HRP20180365T1 - Biciklički heterocikli kao inhibitori fgfr - Google Patents
Biciklički heterocikli kao inhibitori fgfr Download PDFInfo
- Publication number
- HRP20180365T1 HRP20180365T1 HRP20180365TT HRP20180365T HRP20180365T1 HR P20180365 T1 HRP20180365 T1 HR P20180365T1 HR P20180365T T HRP20180365T T HR P20180365TT HR P20180365 T HRP20180365 T HR P20180365T HR P20180365 T1 HRP20180365 T1 HR P20180365T1
- Authority
- HR
- Croatia
- Prior art keywords
- nrc6rd6
- alkyl
- nrc6c
- ora6
- independently selected
- Prior art date
Links
- 125000002618 bicyclic heterocycle group Chemical group 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 33
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 30
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 27
- 150000001875 compounds Chemical class 0.000 claims 26
- 125000005843 halogen group Chemical group 0.000 claims 26
- 125000001424 substituent group Chemical group 0.000 claims 24
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 23
- 150000003839 salts Chemical class 0.000 claims 23
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims 20
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 16
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 16
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims 13
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 12
- 101100310928 Caenorhabditis elegans sra-6 gene Proteins 0.000 claims 12
- -1 -C(O)RA Chemical group 0.000 claims 11
- 125000006568 (C4-C7) heterocycloalkyl group Chemical group 0.000 claims 10
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 10
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 9
- 238000000034 method Methods 0.000 claims 9
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 6
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 5
- 208000035475 disorder Diseases 0.000 claims 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- 101100310920 Caenorhabditis elegans sra-2 gene Proteins 0.000 claims 3
- 208000014767 Myeloproliferative disease Diseases 0.000 claims 3
- 201000007224 Myeloproliferative neoplasm Diseases 0.000 claims 3
- 206010028980 Neoplasm Diseases 0.000 claims 3
- 201000011510 cancer Diseases 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 210000001612 chondrocyte Anatomy 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 2
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 2
- KCTAFCBIIMHTHL-UHFFFAOYSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-(2-morpholin-4-ylethylamino)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NCCN4CCOCC4)=NC=C3C2)=O)=C1F KCTAFCBIIMHTHL-UHFFFAOYSA-N 0.000 claims 2
- JLLPQMNQJBQSRY-UHFFFAOYSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-[2-(4-methylpiperazin-1-yl)ethylamino]spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NCCN4CCN(C)CC4)=NC=C3C2)=O)=C1F JLLPQMNQJBQSRY-UHFFFAOYSA-N 0.000 claims 2
- WLDSTFTUIFOSDT-AWEZNQCLSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-[[(2S)-oxolan-2-yl]methylamino]spiro[1H-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound FC1=C(C(=C(C=C1OC)OC)F)N1CC2=CN=C(C=C2C2(CC2)C1=O)NC[C@H]1OCCC1 WLDSTFTUIFOSDT-AWEZNQCLSA-N 0.000 claims 2
- 201000010028 Acrocephalosyndactylia Diseases 0.000 claims 2
- 101100310926 Caenorhabditis elegans sra-3 gene Proteins 0.000 claims 2
- 101100310927 Caenorhabditis elegans sra-4 gene Proteins 0.000 claims 2
- 206010025323 Lymphomas Diseases 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 230000003553 hypophosphatemic effect Effects 0.000 claims 2
- 239000000825 pharmaceutical preparation Substances 0.000 claims 2
- 208000011580 syndromic disease Diseases 0.000 claims 2
- 201000003896 thanatophoric dysplasia Diseases 0.000 claims 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- 125000006584 (C3-C10) heterocycloalkyl group Chemical group 0.000 claims 1
- FLBAYUMRQUHISI-UHFFFAOYSA-N 1,8-naphthyridine Chemical compound N1=CC=CC2=CC=CN=C21 FLBAYUMRQUHISI-UHFFFAOYSA-N 0.000 claims 1
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- UNVZGXGIFYPFHJ-UHFFFAOYSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-(3-fluoroanilino)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC=4C=C(F)C=CC=4)=NC=C3C2)=O)=C1F UNVZGXGIFYPFHJ-UHFFFAOYSA-N 0.000 claims 1
- NWBYJLBUUNLMHP-UHFFFAOYSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-(methylamino)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound C1=NC(NC)=CC2=C1CN(C=1C(=C(OC)C=C(OC)C=1F)F)C(=O)C21CC1 NWBYJLBUUNLMHP-UHFFFAOYSA-N 0.000 claims 1
- XCGLSKCGLBBYIN-UHFFFAOYSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-(oxan-4-ylamino)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC4CCOCC4)=NC=C3C2)=O)=C1F XCGLSKCGLBBYIN-UHFFFAOYSA-N 0.000 claims 1
- VIWMYZJWZCGRBF-UHFFFAOYSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-(pyridin-2-ylmethylamino)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NCC=4N=CC=CC=4)=NC=C3C2)=O)=C1F VIWMYZJWZCGRBF-UHFFFAOYSA-N 0.000 claims 1
- BFUHISFXTSUKRS-UHFFFAOYSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-(pyridin-3-ylamino)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC=4C=NC=CC=4)=NC=C3C2)=O)=C1F BFUHISFXTSUKRS-UHFFFAOYSA-N 0.000 claims 1
- MVRQRUQUYBUKRR-UHFFFAOYSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-[(1-methylpiperidin-4-yl)amino]spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC4CCN(C)CC4)=NC=C3C2)=O)=C1F MVRQRUQUYBUKRR-UHFFFAOYSA-N 0.000 claims 1
- FVDRKBARHIIISQ-UHFFFAOYSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-[(1-methylpyrazol-4-yl)amino]spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC4=CN(C)N=C4)=NC=C3C2)=O)=C1F FVDRKBARHIIISQ-UHFFFAOYSA-N 0.000 claims 1
- MPIBAVKEXCASBT-UHFFFAOYSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-[(1-methylpyrazol-4-yl)methylamino]spiro[1H-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound FC1=C(C(=C(C=C1OC)OC)F)N1CC2=CN=C(C=C2C2(CC2)C1=O)NCC=1C=NN(C1)C MPIBAVKEXCASBT-UHFFFAOYSA-N 0.000 claims 1
- VVIZKMACHQLJHX-OAHLLOKOSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-[[(1r)-1-phenylethyl]amino]spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(N[C@H](C)C=4C=CC=CC=4)=NC=C3C2)=O)=C1F VVIZKMACHQLJHX-OAHLLOKOSA-N 0.000 claims 1
- VPBADHFSKMXWLX-NSHDSACASA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-[[(2s)-2-hydroxypropyl]amino]spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC[C@H](C)O)=NC=C3C2)=O)=C1F VPBADHFSKMXWLX-NSHDSACASA-N 0.000 claims 1
- QQYBCRVKCIIDMI-ZDUSSCGKSA-N 2-(2,6-difluoro-3,5-dimethoxyphenyl)-6-[[(3s)-oxolan-3-yl]amino]spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(N[C@@H]4COCC4)=NC=C3C2)=O)=C1F QQYBCRVKCIIDMI-ZDUSSCGKSA-N 0.000 claims 1
- PECYZEOJVXMISF-UWTATZPHSA-N 3-amino-D-alanine Chemical compound NC[C@@H](N)C(O)=O PECYZEOJVXMISF-UWTATZPHSA-N 0.000 claims 1
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- VNXKNBMRJYHPDM-UHFFFAOYSA-N 6-(cyclobutylamino)-2-(2,6-difluoro-3,5-dimethoxyphenyl)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC4CCC4)=NC=C3C2)=O)=C1F VNXKNBMRJYHPDM-UHFFFAOYSA-N 0.000 claims 1
- OPTQIQIKSBUZNX-UHFFFAOYSA-N 6-(cyclohexylamino)-2-(2,6-difluoro-3,5-dimethoxyphenyl)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC4CCCCC4)=NC=C3C2)=O)=C1F OPTQIQIKSBUZNX-UHFFFAOYSA-N 0.000 claims 1
- ROWWMGUULGUJPH-UHFFFAOYSA-N 6-(cyclopentylamino)-2-(2,6-difluoro-3,5-dimethoxyphenyl)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC4CCCC4)=NC=C3C2)=O)=C1F ROWWMGUULGUJPH-UHFFFAOYSA-N 0.000 claims 1
- GUPHIFOHCAAWAV-UHFFFAOYSA-N 6-(cyclopropylamino)-2-(2,6-difluoro-3,5-dimethoxyphenyl)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC4CC4)=NC=C3C2)=O)=C1F GUPHIFOHCAAWAV-UHFFFAOYSA-N 0.000 claims 1
- VLUBZJFVIZSEHU-UHFFFAOYSA-N 6-[(3,3-difluorocyclobutyl)amino]-2-(2,6-difluoro-3,5-dimethoxyphenyl)spiro[1h-2,7-naphthyridine-4,1'-cyclopropane]-3-one Chemical compound COC1=CC(OC)=C(F)C(N2C(C3(CC3)C3=CC(NC4CC(F)(F)C4)=NC=C3C2)=O)=C1F VLUBZJFVIZSEHU-UHFFFAOYSA-N 0.000 claims 1
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims 1
- 208000009746 Adult T-Cell Leukemia-Lymphoma Diseases 0.000 claims 1
- 208000016683 Adult T-cell leukemia/lymphoma Diseases 0.000 claims 1
- 208000025490 Apert syndrome Diseases 0.000 claims 1
- 208000003950 B-cell lymphoma Diseases 0.000 claims 1
- 206010005003 Bladder cancer Diseases 0.000 claims 1
- 206010006187 Breast cancer Diseases 0.000 claims 1
- 208000026310 Breast neoplasm Diseases 0.000 claims 1
- YAKXQTYYTVPRSB-SHTZXODSSA-N COc1cc(OC)c(F)c(N2Cc3cnc(N[C@H]4CC[C@H](O)CC4)cc3C3(CC3)C2=O)c1F Chemical compound COc1cc(OC)c(F)c(N2Cc3cnc(N[C@H]4CC[C@H](O)CC4)cc3C3(CC3)C2=O)c1F YAKXQTYYTVPRSB-SHTZXODSSA-N 0.000 claims 1
- 101100150279 Caenorhabditis elegans srb-6 gene Proteins 0.000 claims 1
- 206010008342 Cervix carcinoma Diseases 0.000 claims 1
- 206010009944 Colon cancer Diseases 0.000 claims 1
- 206010066946 Craniofacial dysostosis Diseases 0.000 claims 1
- 208000009283 Craniosynostoses Diseases 0.000 claims 1
- 201000006526 Crouzon syndrome Diseases 0.000 claims 1
- 206010013883 Dwarfism Diseases 0.000 claims 1
- 206010014733 Endometrial cancer Diseases 0.000 claims 1
- 206010014759 Endometrial neoplasm Diseases 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 208000000461 Esophageal Neoplasms Diseases 0.000 claims 1
- 208000032027 Essential Thrombocythemia Diseases 0.000 claims 1
- 108091008794 FGF receptors Proteins 0.000 claims 1
- 208000005050 Familial Hypophosphatemic Rickets Diseases 0.000 claims 1
- 208000022072 Gallbladder Neoplasms Diseases 0.000 claims 1
- 208000017604 Hodgkin disease Diseases 0.000 claims 1
- 208000021519 Hodgkin lymphoma Diseases 0.000 claims 1
- 208000010747 Hodgkins lymphoma Diseases 0.000 claims 1
- 208000029663 Hypophosphatemia Diseases 0.000 claims 1
- 208000009289 Jackson-Weiss syndrome Diseases 0.000 claims 1
- 208000008839 Kidney Neoplasms Diseases 0.000 claims 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 1
- 208000031422 Lymphocytic Chronic B-Cell Leukemia Diseases 0.000 claims 1
- 206010052178 Lymphocytic lymphoma Diseases 0.000 claims 1
- 208000034578 Multiple myelomas Diseases 0.000 claims 1
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims 1
- 208000015914 Non-Hodgkin lymphomas Diseases 0.000 claims 1
- 206010030155 Oesophageal carcinoma Diseases 0.000 claims 1
- 208000005072 Oncogenic osteomalacia Diseases 0.000 claims 1
- 206010033128 Ovarian cancer Diseases 0.000 claims 1
- 206010061535 Ovarian neoplasm Diseases 0.000 claims 1
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims 1
- 201000004014 Pfeiffer syndrome Diseases 0.000 claims 1
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 1
- 206010060862 Prostate cancer Diseases 0.000 claims 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 1
- 206010038389 Renal cancer Diseases 0.000 claims 1
- 208000000453 Skin Neoplasms Diseases 0.000 claims 1
- 208000005718 Stomach Neoplasms Diseases 0.000 claims 1
- 208000024770 Thyroid neoplasm Diseases 0.000 claims 1
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims 1
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 claims 1
- 208000033559 Waldenström macroglobulinemia Diseases 0.000 claims 1
- 208000031878 X-linked hypophosphatemia Diseases 0.000 claims 1
- 208000035724 X-linked hypophosphatemic rickets Diseases 0.000 claims 1
- 208000017733 acquired polycythemia vera Diseases 0.000 claims 1
- 201000006966 adult T-cell leukemia Diseases 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 201000003674 autosomal dominant hypophosphatemic rickets Diseases 0.000 claims 1
- 201000003672 autosomal recessive hypophosphatemic rickets Diseases 0.000 claims 1
- 210000004027 cell Anatomy 0.000 claims 1
- 201000010881 cervical cancer Diseases 0.000 claims 1
- 230000001684 chronic effect Effects 0.000 claims 1
- 208000029742 colonic neoplasm Diseases 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 201000004101 esophageal cancer Diseases 0.000 claims 1
- 102000052178 fibroblast growth factor receptor activity proteins Human genes 0.000 claims 1
- 201000010175 gallbladder cancer Diseases 0.000 claims 1
- 206010017758 gastric cancer Diseases 0.000 claims 1
- 208000005017 glioblastoma Diseases 0.000 claims 1
- 201000010536 head and neck cancer Diseases 0.000 claims 1
- 208000014829 head and neck neoplasm Diseases 0.000 claims 1
- 201000010072 hypochondroplasia Diseases 0.000 claims 1
- 238000000338 in vitro Methods 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 201000010982 kidney cancer Diseases 0.000 claims 1
- 208000032839 leukemia Diseases 0.000 claims 1
- 201000007270 liver cancer Diseases 0.000 claims 1
- 208000014018 liver neoplasm Diseases 0.000 claims 1
- 201000005202 lung cancer Diseases 0.000 claims 1
- 208000020816 lung neoplasm Diseases 0.000 claims 1
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- XNPFFUMEQYIEGJ-UHFFFAOYSA-N methyl n-[7-(2,6-difluoro-3,5-dimethoxyphenyl)-6-oxospiro[8h-2,7-naphthyridine-5,1'-cyclopropane]-3-yl]carbamate Chemical compound C1=NC(NC(=O)OC)=CC2=C1CN(C=1C(=C(OC)C=C(OC)C=1F)F)C(=O)C21CC1 XNPFFUMEQYIEGJ-UHFFFAOYSA-N 0.000 claims 1
- 206010028537 myelofibrosis Diseases 0.000 claims 1
- 201000002528 pancreatic cancer Diseases 0.000 claims 1
- 208000008443 pancreatic carcinoma Diseases 0.000 claims 1
- 208000037244 polycythemia vera Diseases 0.000 claims 1
- 208000003476 primary myelofibrosis Diseases 0.000 claims 1
- 125000006514 pyridin-2-ylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims 1
- 201000009410 rhabdomyosarcoma Diseases 0.000 claims 1
- 201000000849 skin cancer Diseases 0.000 claims 1
- 201000011549 stomach cancer Diseases 0.000 claims 1
- 201000002510 thyroid cancer Diseases 0.000 claims 1
- 201000005112 urinary bladder cancer Diseases 0.000 claims 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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Claims (23)
1. Spoj formule IIIa:
[image]
ili njegova farmaceutski prihvatljiva sol, naznačen time da:
R2 i R5 su svaki neovisno odabrani između H, halo, C1-6 alkil, C2-6 alkenil, C2-6 alkinil, C1-6 haloalkil, ciklopropil, CN, ORa, SRa, C(O)Rb, C(O)NRcRd, C(O)ORa, OC(O)Rb, OC(O)NRcRd, NRcRd, NRcC(O)Rb, NRcC(O)ORa, NRcC(O)NRcRd, C(=NRe)Rb, C(=NRe)NRcRd, NRcC(=NRe)NRcRd, NRcS(O)Rb, NRcS(O)2Rb, NRcS(O)2NRcRd, S(O)Rb, S(O)NRcRd, S(O)2Rb, i S(O)2NRcRd;
R6 je H, halo, C1-6 alkil, C2-6 alkenil, C2-6 alkinil, C1-6 haloalkil, C6-10 aril, C3-10 cikloalkil, 5-10 člani heteroaril, 4-10 člani heterocikloalkil, CN, NO2, ORa2, SRa2, C(O)Rb2, C(O)NRc2Rd2, C(O)ORa2, OC(O)Rb2, OC(O)NRc2Rd2, NRc2Rd2, NRc2C(O)Rb2, NRc2C(O)ORa2, NRc2C(O)NRc2Rd2, C(=NRe2)Rb2, C(=NRe2)NRc2Rd2, NRc2C(=NRe2)NRc2Rd2, NRc2S(O)Rb2, NRc2S(O)2Rb2, NRc2S(O)2NRc2Rd2, S(O)Rb2, S(O)NRc2Rd2, S(O)2Rb2, ili S(O)2NRc2Rd2; pri čemu navedeni C1-6 alkil, C2-6 alkenil, C2-6 alkinil, C6-10 aril, C3-10 cikloalkil, 5-10 člani heteroaril, i 4-10 člani heterocikloalkil su svaki proizvoljno supstituirani s 1, 2, 3, 4, ili 5 supstituenata koji su neovisno odabrani od R6a;
svaki R6a je neovisno odabran od Cy1, halo, C1-6 alkil, C2-6 alkenil, C2-6 alkinil, C1-6 haloalkil, CN, NO2, ORa2, SRa2, C(O)Rb2, C(O)NRc2Rd2, C(O)ORa2, OC(O)Rb2, OC(O)NRc2Rd2, C(=NRe2)NRc2Rd2, NRc2C(=NRe2)NRc2Rd2, NRc2Rd2, NRc2C(O)Rb2, NRc2C(O)ORa2, NRc2C(O)NRc2Rd2, NRc2S(O)Rb2, NRc2S(O)2Rb2, NRc2S(O)2NRc2Rd2, S(O)Rb2, S(O)NRc2Rd2, S(O)2Rb2, i S(O)2NRc2Rd2, pri čemu navedeni C1-6 alkil, C2-6 alkenil, i C2-6 alkinil su svaki proizvoljno supstituirani s 1, 2, ili 3 supstituenta koji su neovisno odabrani od Cy1, halo, CN, NO2, ORa2, SRa2, C(O)Rb2, C(O)NRc2Rd2, C(O)ORa2, OC(O)Rb2, OC(O)NRc2Rd2, C(=NRe2)NRc2Rd2, NRc2C(=NRe2)NRc2Rd2, NRc2Rd2, NRc2C(O)Rb2, NRc2C(O)ORa2, NRc2C(O)NRc2Rd2, NRc2S(O)Rb2, NRc2S(O)2Rb2, NRc2S(O)2NRc2Rd2, S(O)Rb2, S(O)NRc2Rd2, S(O)2Rb2, i S(O)2NRc2Rd2; R7 i R8 su svaki neovisno odabrani od H, C1-6 alkil, C2-6 alkenil, C2-6 alkinil, -C(O)RA, S(O)RA, S(O)2RA, C6-10 aril, C3-10 cikloalkil, 5-10 članog heteroarila, 4-10 članog heterocikloalkila, C6-10 aril-C1-4 alkil, C3-10 cikloalkil-C1-4 alkil, (5-10 člani heteroaril)-C1-4 alkil, i (4-10 člani heterocikloalkil)-C1-4 alkil, pri čemu navedeni C1-6 alkil, C2-6 alkenil, C2-6 alkinil, C6-10 aril, C3-10 cikloalkil, 5-10 člani heteroaril, 4-10 člani heterocikloalkil, C6-10 aril-C1-4 alkil, C3-10 cikloalkil-C1-4 alkil, (5-10 člani heteroaril)-C1-4 alkil, i (4-10 člani heterocikloalkil)-C1-4 alkil su svaki proizvoljno supstituirani s 1, 2, 3, 4, ili 5 supstituenata koji su neovisno odabrani od R7a;
svaki R7a je neovisno odabran od Cy2, halo, C1-6 alkil, C2-6 alkenil, C2-6 alkinil, C1-6 haloalkil, CN, NO2, ORa3, SRa3, C(O)Rb3, C(O)NRc3Rd3, C(O)ORa3, OC(O)Rb3, OC(O)NRc3Rd3, C(=NRe3)NRc3Rd3, NRC3C(=NRe3)NRc3Rd3, NRc3Rd3 , NRc3C(O)Rb3, NRc3C(O)ORa3, NRc3C(O)NRc3Rd3, NRc3S(O)Rb3, NRC3S(O)2Rb3, NRc3S(O)2NRc3Rd3, S(O)Rb3, S(O)NRc3Rd3, S(O)2Rb3, i S(O)2NRc3Rd3, pri čemu navedeni C1-6 alkil, C2-6 alkenil, i C2-6 alkinil su svaki proizvoljno supstituirani s 1, 2, ili 3 supstituenta koji su neovisno odabrani od Cy2, halo, CN, NO2, ORa3, SRa3, C(O)Rb3, C(O)NRc3Rd3, C(O)ORa3, OC(O)Rb3, OC(O)NRc3Rd3, C(=NRe3)NRc3Rd3, NRC3C(=NRe3)NRc3Rd3, NRc3Rd3, NRc3C(O)Rb3, NRc3C(O)ORa3, NRc3C(O)NRc3Rd3, NRc3S(O)Rb3, NRc3S(O)2Rb3, NRc3S(O)2NRc3Rd3, S(O)Rb3, S(O)NRc3Rd3, S(O)2Rb3, i S(O)2NRc3Rd3;
R10 i R11 zajedno s ugljikovim atomom za koji su vezani tvore 3-, 4-, 5-, 6-, ili 7-članu cikloalkil skupinu ili 4-, 5-, 6-, ili 7-članu heterocikloalkil skupinu, svaku proizvoljno supstituiranu sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od Cy3, C1-6 alkil, C1-6 haloalkil, halo, CN, ORa4, SRa4, C(O)Rb4, C(O)NRc4Rd4, C(O)ORa4, OC(O)Rb4, OC(O)NRc4Rd4, NRc4Rd4, NRc4C(O)Rb4, NRc4C(O)NRc4Rd4, NRc4C(O)ORa4, C(=NRe4)NRc4Rd4, NRc4C(=NRe4)NRc4Rd4, S(O)Rb4, S(O)NRc4Rd4, S(O)2Rb4, NRc4S(O)2Rb4, NRc4S(O)2NRc4Rd4, i S(O)2NRc4Rd4, pri čemu navedeni C1-6 alkil je proizvoljno supstituiran s 1, 2, ili 3 supstituenta koji su neovisno odabrani od Cy3, halo, CN, ORa4, SRa4, C(O)Rb4, C(O)NRc4Rd4, C(O)ORa4, OC(O)Rb4, OC(O)NRc4Rd4, NRc4Rd4, NRc4C(O)Rb4, NRc4C(O)NRc4Rd4, NRc4C(O)ORa4, C(=NRe4)NRc4Rd4, NRc4C(=NRe4)NRc4Rd4, S(O)Rb4, S(O)NRc4Rd4, S(O)2Rb4, NRc4S(O)2Rb4, NRc4S(O)2NRc4Rd4, i S(O)2NRc4Rd4;
svaki RA je neovisno odabran od H, C1-6 alkil, C1-6 alkoksi, C6-10 aril, C3-10 cikloalkil, 5-10 članog heteroarila, 4-10 članog heterocikloalkila, C6-10 aril-C1-4 alkil, C3-10 cikloalkil-C1-4 alkil, (5-10 člani heteroaril)-C1-4 alkil, i (4-10 člani heterocikloalkil)-C1-4 alkil, pri čemu navedeni C1-6 alkil, C1-6 alkoksi, C6-10 aril, C3-10 cikloalkil, 5-10 člani heteroaril, 4-10 člani heterocikloalkil, C6-10 aril-C1-4 alkil, C3-10 cikloalkil-C1-4 alkil, (5-10 člani heteroaril)-C1-4 alkil, i (4-10 člani heterocikloalkil)-C1-4 alkil su svaki proizvoljno supstituirani s 1, 2, ili 3 supstituenta koji su neovisno odabrani od R7a; Cy1, Cy2, i Cy3 su svaki neovisno odabrani od C6-10 aril, C3-10 cikloalkil, 5-10 članog heteroarila, i 4-10 članog heterocikloalkila, svaki od kojih je proizvoljno supstituiran s 1, 2, 3, 4, ili 5 supstituenata koji su neovisno odabrani od halo, C1-6 alkil, C2-6 alkenil, C2-6 alkinil, C1-6 haloalkil, C6-10 aril, C3-10 cikloalkil, 5-10 člani heteroaril, 3-10 člani heterocikloalkil, CN, NO2, ORa5, SRa5, C(O)Rb5, C(O)NRc5Rd5, C(O)ORa5, OC(O)Rb5, OC(O)NRc5Rd5, NRc5Rd5, NRc5C(O)Rb5, NRc5C(O)ORa5, NRc5C(O)NRc5Rd5, C(=NRe5)Rb5, C(=NRe5)NRc5Rd5, NRc5C(=NRe5)NRc5Rd5, NRc5S(O)Rb5, NRcSS(O)2Rb5, NRc5S(O)2NRc5Rd5, S(O)Rb5, S(O)NRc5Rd5, S(O)2Rb5, i S(O)2NRc5Rd5; pri čemu navedeni C1-6 alkil, C2-6 alkenil, C2-6 alkinil, C6-10 aril, C3-10 cikloalkil, 5-10 člani heteroaril, i 4-10 člani heterocikloalkil su svaki proizvoljno supstituirani s 1, 2, 3, 4, ili 5 supstituenata koji su neovisno odabrani od halo, C1-6 alkil, C2-6 alkenil, C2-6 alkinil, C1-6 haloalkil, CN, NO2, ORa5, SRa5, C(O)Rb5, C(O)NRc5Rd5, C(O)ORa5, OC(O)Rb5, OC(O)NRc5Rd5, C(=NRe5)NRc5Rd5, NRc5C(=NRe5)NRc5Rd5, NRc5Rd5, NRc5C(O)Rb5, NRc5C(O)ORa5, NRc5C(O)NRc5Rd5, NRc5S(O)Rb5, NRc5S(O)2Rb5, NRc5S(O)2NRc5Rd5, S(O)Rb5, S(O)NRc5Rd5, S(O)2Rb5, i S(O)2NRc5Rd5; svaki Ra, Rb, Rc, i Rd je neovisno odabran od H, C1-6 alkil, C1-4 haloalkil, C2-6 alkenil, C2-6 alkinil, i ciklopropil, pri čemu navedeni C1-6 alkil, C2-6 alkenil, C2-6 alkinil, i ciklopropil je proizvoljno supstituiran s 1, 2, ili 3 supstituenta koji su neovisno odabrani od C1-4 alkil, C1-4 haloalkil, halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6;
svaki Ra2, Rb2, Rc2, Rd2, Ra3, Rb3, Rc3, Rd3, Ra4, Rb4, Rc4, Rd4, Ra5, Rb5, Rc5, i Rd5 je neovisno odabran od H, C1-6 alkil, C1-4 haloalkil, C2-6 alkenil, C2-6 alkinil, C6-10 aril, C3-10 cikloalkil, 5-10 članog heteroarila, 4-10 članog heterocikloalkila, C6-10 aril-C1-4 alkil, C3-10 cikloalkil-C1-4 alkil, (5-10 člani heteroaril)-C1-4 alkil, i (4-10 člani heterocikloalkil)-C1-4 alkil, pri čemu navedeni C1-6 alkil, C2-6 alkenil, C2-6 alkinil, C6-10 aril, C3-10 cikloalkil, 5-10 članog heteroarila, 4-10 članog heterocikloalkila, C6-10 aril-C1-4 alkil, C3-10 cikloalkil-C1-4 alkil, (5-10 člani heteroaril)-C1-4 alkil, i (4-10 člani heterocikloalkil)-C1-4 alkil je proizvoljno supstituiran s 1, 2, 3, 4, ili 5 supstituenata koji su neovisno odabrani od C1-4 alkil, C1-4 haloalkil, halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6;
ili bilo koji Rc i Rd zajedno sa N atomom za koji su vezani tvore 4-, 5-, 6-, ili 7-članu heterocikloalkil skupinu proizvoljno supstituiranu sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od C1-6 alkil, C3-7 cikloalkil, 4-7 člani heterocikloalkil, C6-10 aril, 5-6 članog heteroarila, C1-6 haloalkil, halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6, pri čemu navedeni C1-6 alkil, C3-7 cikloalkil, 4-7 člani heterocikloalkil, C6-10 aril, i 5-6 člani heteroaril su proizvoljno supstituirani sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6;
ili bilo koji Rc2 i Rd2 zajedno s N atomom za koji su vezani tvore 4-, 5-, 6-, ili 7-člani heterocikloalkil skupinu proizvoljno supstituiranu sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od C1-6 alkil, C3-7 cikloalkil, 4-7 članog heterocikloalkila, C6-10 aril, i 5-6 članog heteroarila, C1-6 haloalkil, halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6, pri čemu navedeni C1-6 alkil, C3-7 cikloalkil, 4-7 člani heterocikloalkil, C6-10 aril, i 5-6 člani heteroaril su proizvoljno supstituirani sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6;
ili bilo koji Rc3 i Rd3 zajedno sa N atomom za koji su vezani tvore 4-, 5-, 6-, ili 7-članu heterocikloalkil skupinu proizvoljno supstituiranu sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od C1-6 alkil, C3-7 cikloalkil, 4-7 članog heterocikloalkila, C6-10 aril, 5-6 članog heteroarila, C1-6 haloalkil, halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRC6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6, pri čemu navedeni C1-6 alkil, C3-7 cikloalkil, 4-7 člani heterocikloalkil, C6-10 aril, i 5-6 člani heteroaril su proizvoljno supstituirani sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6;
ili bilo koji Rc4 i Rd4 zajedno sa N atomom za koji su vezani tvore 4-, 5-, 6-, ili 7-članu heterocikloalkil skupinu proizvoljno supstituiranu s 1, 2, ili 3 supstituenta koji su neovisno odabrani od C1-6 alkil, C3-7 cikloalkil, 4-7 članog heterocikloalkila, C6-10 aril, 5-6 članog heteroarila, C1-6 haloalkil, halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6, pri čemu navedeni C1-6 alkil, C1-4 cikloalkil, 4-7 člani heterocikloalkil, C6-10 aril, i 5-6 člani heteroaril su proizvoljno supstituirani sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6;
ili bilo koji Rc5 i Rd5 zajedno sa N atomom za koji su vezani tvore 4-, 5-, 6-, ili 7-članu heterocikloalkil skupinu proizvoljno supstituiranu s 1, 2, ili 3 supstituenta koji su neovisno odabrani od C1-6 alkil, C3-7 cikloalkil, 4-7 članog heterocikloalkila, C6-10 aril, 5-6 članog heteroarila, C1-6 haloalkil, halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6, pri čemu navedeni C1-6 alkil, C3-7 cikloalkil, 4-7 člani heterocikloalkil, C6-10 aril, i 5-6 člani heteroaril su proizvoljno supstituirani sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od halo, CN, ORa6, SRa6, C(O)Rb6, C(O)NRc6Rd6, C(O)ORa6, OC(O)Rb6, OC(O)NRc6Rd6, NRc6Rd6, NRc6C(O)Rb6, NRc6C(O)NRc6Rd6, NRc6C(O)ORa6, C(=NRe6)NRc6Rd6, NRc6C(=NRe6)NRc6Rd6, S(O)Rb6, S(O)NRc6Rd6, S(O)2Rb6, NRc6S(O)2Rb6, NRc6S(O)2NRc6Rd6, i S(O)2NRc6Rd6;
svaki od Re, Re2, Re3, Re4, i Re5 je neovisno odabran od H, C1-4 alkil, CN, ORa6, SRb6, S(O)2Rb6, C(O)Rb6, S(O)2NRc6Rd6, i C(O)NRc6Rd6;
svaki od Ra6, Rb6, Rc6, i Rd6 je neovisno odabran od H, C1-4 alkil, C1-4 haloalkil, C2-4 alkenil, i C2-4 alkinil, pri čemu navedeni C1-4 alkil, C2-4 alkenil, i C2-4 alkinil su proizvoljno supstituirani sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od OH, CN, amino, halo, C1-4 alkil, C1-4 alkoksi, C1-4 alkiltio, C1-4 alkilamino, di(C1-4 alkil)amino, C1-4 haloalkil, i C1-4 haloalkoksi;
ili svaki Rc6 i Rd6 zajedno sa N atomom za koji su vezani tvore 4-, 5-, 6-, ili 7-članu heterocikloalkil skupinu proizvoljno supstituiranu sa 1, 2, ili 3 supstituenta koji su neovisno odabrani od OH, CN, amino, halo, C1-6 alkil, C1-4 alkoksi, C1-4 alkiltio, C1-4 alkilamino, di(C1-4 alkil)amino, C1-4 haloalkil, i C1-4 haloalkoksi;
i svaki Re6 je neovisno odabran od H, C1-4 alkil, i CN.
2. Spoj prema zahtjevu 1, ili njegova farmaceutski prihvatljiva sol, naznačen time da R2 je halo.
3. Spoj prema zahtjevu 1, ili njegova farmaceutski prihvatljiva sol, naznačen time da R2 je fluoro.
4. Spoj prema bilo kojem od zahtjeva 1-3, ili njegova farmaceutski prihvatljiva sol, naznačen time da R5 je halo.
5. Spoj prema bilo kojem od zahtjeva 1-3, ili njegova farmaceutski prihvatljiva sol, naznačen time da R5 je fluoro.
6. Spoj prema bilo kojem od zahtjeva 1-5, ili njegova farmaceutski prihvatljiva sol, naznačen time da R6 je H.
7. Spoj prema bilo kojem od zahtjeva 1-6, ili njegova farmaceutski prihvatljiva sol, naznačen time da R10 i R11 zajedno s ugljikovim atomom za koji su vezani tvore 3-, 4-, 5-, 6-, ili 7-članu cikloalkil skupinu.
8. Spoj prema bilo kojem od zahtjeva 1-6, ili njegova farmaceutski prihvatljiva sol, naznačen time da R10 i R11 zajedno s ugljikovim atomom za koji su vezani tvore ciklopropil skupinu.
9. Spoj prema bilo kojem od zahtjeva 1-8, ili njegova farmaceutski prihvatljiva sol, naznačen time da su R7 i R8 svaki neovisno odabrani od H, C1-6 alkil, -C(O)RA, C6-10 aril, C3-10 cikloalkil, 5-10 članog heteroarila, 4-10 članog heterocikloalkila, C6-10 aril-C1-4 alkil, (5-10 člani heteroaril)-C1-4 alkil, i (4-10 člani heterocikloalkil)-C1-4 alkil, pri čemu navedeni C1-6 alkil, C6-10 aril, C3-10 cikloalkil, 5-10 člani heteroaril, 4-10 člani heterocikloalkil, (5-10 člani heteroaril)-C1-4 alkil, i (4-10 člani heterocikloalkil)-C1-4 alkil su svaki proizvoljno supstituirani s 1, 2, 3, 4, ili 5 supstituenata koji su neovisno odabrani od R7a.
10. Spoj prema bilo kojem od zahtjeva 1-8, ili njegova farmaceutski prihvatljiva sol, naznačen time da su R7 i R8 svaki neovisno odabrani između H, 2-hidroksipropil, -C(O)OCH3, 3-fluorofenil, ciklopropil, ciklobutil, 3,3-difluoro-ciklobutil, ciklopentil, cikloheksil, 4-hidroksicikloheksil, metil, 1-metil-1H-pirazol-4-il, piridin-3-il, N-metil-piperidin-4-il, tetrahidro-2H-piran-4-il, tetrahidrofuran-3-il, 1-feniletil, (1-metil-1H-pirazol-4-il)metil, 2-morfolino-4-iletil, piridin-2-ilmetil, N-metilpiperazin-1-iletil, i tetrahidrofuran-2-il-metil.
11. Spoj prema bilo kojem od zahtjeva 1-8, ili njegova farmaceutski prihvatljiva sol, naznačen time da jedan od R7 i R8 je H.
12. Spoj prema bilo kojem od zahtjeva 1-8, ili njegova farmaceutski prihvatljiva sol, naznačen time da su R7 i R8 svaki H.
13. Spoj prema zahtjevu 1 naznačen time da je odabran između:
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-[(2-morfolin-4-iletil)amino]-1’,2’-dihidro-3’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’-on;
6’-amino-2’-(2,6-difluoro-3,5-dimetoksifenil)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(metilamino)-1’,2’-dihidro-3’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’-on;
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(tetrahidro-2H-piran-4-ilamino)-1’,2’-dihidro-3’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’-on;
(S)-2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(2-hidroksipropilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(piridin-2-ilmetilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
(S)-2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(tetrahidrofuran-3-ilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(2-(4-metilpiperazin-1-il)etilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
metil 2’-(2,6-difluoro-3,5-dimetoksifenil)-3’-okso-2’,3’-dihidro-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridine]-6’-ilkarbamat;
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(piridin-3-ilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(3-fluorofenilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
6’-(ciklopentilamino)-2’-(2,6-difluoro-3,5-dimetoksifenil)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
(S)-2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-((tetrahidrofuran-2-il)metilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(1-metil-1H-pirazol-4-ilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-((1-metil-1H-pirazol-4-il)metilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
(R)-2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(1-feniletilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
6’-(cikloheksilamino)-2’-(2,6-difluoro-3,5-dimetoksifenil)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(trans-4-hidroksicikloheksilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
6’-(ciklopropilamino)-2’-(2,6-difluoro-3,5-dimetoksifenil)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
6’-(ciklobutilamino)-2’-(2,6-difluoro-3,5-dimetoksifenil)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(3,3-difluorociklobutilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on; i
2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(1-metilpiperidin-4-ilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on;
ili farmaceutski prihvatljive soli bilo kojeg od prethodnih.
14. Spoj prema zahtjevu 1, naznačen time da je spoj 2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-[(2-morfolin-4-iletil)amino]-1’,2’-dihidro-3’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’-on, ili njegova farmaceutski prihvatljiva sol.
15. Spoj prema zahtjevu 1, naznačen time da je spoj 2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-(2-(4-metilpiperazin-1-il)etilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on, ili njegova farmaceutski prihvatljiva sol.
16. Spoj prema zahtjevu 1, naznačen time da je spoj (S)-2’-(2,6-difluoro-3,5-dimetoksifenil)-6’-((tetrahidrofuran-2-il)metilamino)-1’H-spiro[ciklopropan-1,4’-[2,7]naftiridin]-3’(2’H)-on, ili njegova farmaceutski prihvatljiva sol.
17. Farmaceutski pripravak naznačen time da sadrži spoj prema bilo kojem od zahtjeva 14-16, ili njegovu farmaceutski prihvatljivu sol, te barem jedan farmaceutski prihvatljiv nosač.
18. Farmaceutski pripravak naznačen time da sadrži spoj prema bilo kojem od zahtjeva 1 do 13, ili njegovu farmaceutski prihvatljivu sol, te barem jedan farmaceutski prihvatljiv nosač.
19. Postupak inhibiranja FGFR enzima naznačen time da sadrži dovođenje u kontakt navedenog enzima in vitro sa spojem prema bilo kojem od zahtjeva 1 do 16, ili njegovom farmaceutski prihvatljivom soli.
20. Spoj prema bilo kojem od zahtjeva 1 do 16, ili njegova farmaceutski prihvatljiva sol, za upotrebu u:
a) postupku liječenja raka kod pacijenta; ili
b) postupku liječenja raka kod pacijenta pri čemu je navedeni rak odabran od raka mjehura, raka dojke, raka grlića maternice, raka debelog crijeva, raka endometrija, raka želudca, raka glave i vrata, raka bubrega, raka jetre, raka pluća, raka jajnika, raka prostate, raka jednjaka, raka žučni, raka gušterače, raka štitnjače, raka kože, leukemije, multiplog mijeloma, kroničnog limfoma limfocita, leukemije T-stanica odraslih, limfoma B-stanica, akutne mijeloidne leukemije, Hodgkinovog ili ne-Hodgkinovog limfoma, Walden-stromove makroglobulinemije, limfoma vlasastih stanica, Burketovog limfoma, glioblastoma, melanoma, i rabdosarkoma.
21. Spoj prema bilo kojem od zahtjeva 1 do 16, ili njegova farmaceutski prihvatljiva sol, za upotrebu u:
a) postupku liječenja mijeloproliferativnog poremećaja kod pacijenta; ili
b) postupku liječenja mijeloproliferativnog poremećaja kod pacijenta pri čemu je navedeni mijeloproliferativni poremećaj odabran od policitemije vera, esencijalne trombocitemije, i primarne mijelofibroze.
22. Spoj prema bilo kojem od zahtjeva 1 do 16, ili njegova farmaceutski prihvatljiva sol, za upotrebu u:
a) postupku liječenja poremećaja skeleta ili kondrocita kod pacijenata; ili
b) postupku liječenja poremećaja skeleta ili kondrocita kod pacijenta pri čemu je navedeni poremećaj skeleta ili kondrocita odabran od ahrondroplazije, hipohondroplazije, patuljastog rasta, tanatoforne displazije (TD), Apertovog sindroma, Crouzonovog sindroma, sindroma Jackson-Weiss, Beare-Stevensonov sindrom kružno izuvijane kože, Pfeifferovog sindroma, i sindroma kraniostenoze.
23. Spoj prema bilo kojem od zahtjeva 1 do 16, ili njegova farmaceutski prihvatljiva sol, za upotrebu u:
a) postupku liječenja poremećaja hipofosfatemije kod pacijenta; ili
b) postupku liječenja poremećaja hipofosfatemije kod pacijenta pri čemu navedeni poremećaj hipofosfatemije je hipofosfatemični rahitis u vezi sa X kromosomom, autosomni recesivni hipofosfatemični rahitis, autosomni dominantni hipofosfatemični rahitis, i osteomalacija izazvana tumorom.
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---|---|---|---|---|
US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
LT3495367T (lt) | 2012-06-13 | 2021-02-25 | Incyte Holdings Corporation | Pakeistieji tricikliniai junginiai, kaip fgfr inhibitoriai |
US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
SI2986610T1 (en) | 2013-04-19 | 2018-04-30 | Incyte Holdings Corporation | Bicyclic heterocycles as inhibitors of FGFR |
US10124003B2 (en) | 2013-07-18 | 2018-11-13 | Taiho Pharmaceutical Co., Ltd. | Therapeutic agent for FGFR inhibitor-resistant cancer |
US20160193210A1 (en) | 2013-07-18 | 2016-07-07 | Taiho Pharmaceutical Co., Ltd. | Antitumor drug for intermittent administration of fgfr inhibitor |
US9266883B2 (en) | 2013-10-25 | 2016-02-23 | Novartis Ag | Ring-fused bicyclic pyridyl derivatives as FGFR4 inhibitors |
US20180185341A1 (en) | 2014-10-03 | 2018-07-05 | Novartis Ag | Use of ring-fused bicyclic pyridyl derivatives as fgfr4 inhibitors |
WO2016064960A1 (en) * | 2014-10-22 | 2016-04-28 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
US9694084B2 (en) | 2014-12-23 | 2017-07-04 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
SG10201913036RA (en) * | 2015-02-20 | 2020-02-27 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
US9802917B2 (en) | 2015-03-25 | 2017-10-31 | Novartis Ag | Particles of N-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-7-formyl-6-((4-methyl-2-oxopiperazin-1-yl)methyl)-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxamide |
CA2980888C (en) | 2015-03-31 | 2018-03-06 | Taiho Pharmaceutical Co., Ltd. | Crystal of 3,5-disubstituted benzene alkynyl compound |
TWI782906B (zh) * | 2016-03-04 | 2022-11-11 | 日商大鵬藥品工業股份有限公司 | 惡性腫瘤治療用製劑及組合物 |
US11883404B2 (en) | 2016-03-04 | 2024-01-30 | Taiho Pharmaceuticals Co., Ltd. | Preparation and composition for treatment of malignant tumors |
CN111689959B (zh) * | 2016-05-27 | 2022-04-01 | 石药集团中奇制药技术(石家庄)有限公司 | 作为fgfr4抑制剂的杂环化合物 |
CN107459519A (zh) * | 2016-06-06 | 2017-12-12 | 上海艾力斯医药科技有限公司 | 稠合嘧啶哌啶环衍生物及其制备方法和应用 |
WO2018160076A1 (en) * | 2017-03-03 | 2018-09-07 | Auckland Uniservices Limited | Fgfr kinase inhibitors and pharmaceutical uses |
AR111960A1 (es) * | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
WO2018218197A2 (en) * | 2017-05-26 | 2018-11-29 | Board Of Regents, The University Of Texas System | Tetrahydropyrido[4,3-d]pyrimidine inhibitors of atr kinase |
CN111867590B (zh) | 2017-07-13 | 2023-11-17 | 德州大学系统董事会 | Atr激酶的杂环抑制剂 |
CN112218631B (zh) | 2018-03-16 | 2023-12-22 | 德州大学系统董事会 | Atr激酶的杂环抑制剂 |
TWI790364B (zh) | 2018-03-19 | 2023-01-21 | 日商大鵬藥品工業股份有限公司 | 包含烷基硫酸鈉之醫藥組合物 |
WO2019213544A2 (en) | 2018-05-04 | 2019-11-07 | Incyte Corporation | Solid forms of an fgfr inhibitor and processes for preparing the same |
EP3788046A1 (en) | 2018-05-04 | 2021-03-10 | Incyte Corporation | Salts of an fgfr inhibitor |
US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
AU2020242287A1 (en) | 2019-03-21 | 2021-09-02 | INSERM (Institut National de la Santé et de la Recherche Médicale) | A Dbait molecule in combination with kinase inhibitor for the treatment of cancer |
US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
US12122767B2 (en) | 2019-10-01 | 2024-10-22 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
JP2022552324A (ja) | 2019-10-14 | 2022-12-15 | インサイト・コーポレイション | Fgfr阻害剤としての二環式複素環 |
WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
GB201915828D0 (en) * | 2019-10-31 | 2019-12-18 | Cancer Research Tech Ltd | Compounds, compositions and therapeutic uses thereof |
WO2021089791A1 (en) | 2019-11-08 | 2021-05-14 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
CN115151539A (zh) | 2019-12-04 | 2022-10-04 | 因赛特公司 | Fgfr抑制剂的衍生物 |
US11897891B2 (en) | 2019-12-04 | 2024-02-13 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
EP4114468A1 (en) * | 2020-03-02 | 2023-01-11 | The Johns Hopkins University | Glucose triptolide conjugates and uses thereof |
CN111960932B (zh) * | 2020-09-16 | 2022-11-08 | 沈阳药科大学 | 二氯雷琐酚类化合物及其制备方法和医药用途 |
CA3215903A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
CA3220274A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
CN113527311B (zh) * | 2021-08-23 | 2022-05-06 | 中南大学湘雅医院 | Fgfr4抑制剂、组合物及其在药物制备中的用途 |
WO2023039828A1 (en) * | 2021-09-17 | 2023-03-23 | Nutshell Biotech (Shanghai) Co., Ltd. | Fused ring compounds as inhibitors of fgfr4 tyrosine kinases |
IL312886A (en) | 2021-11-22 | 2024-07-01 | Incyte Corp | Combined treatment that includes a Pegfer inhibitor and a Kras inhibitor |
WO2024206858A1 (en) | 2023-03-30 | 2024-10-03 | Revolution Medicines, Inc. | Compositions for inducing ras gtp hydrolysis and uses thereof |
Family Cites Families (811)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE280853C (hr) | ||||
US850370A (en) | 1906-06-05 | 1907-04-16 | William L Hynes | Water-automobile. |
DE2156720A1 (de) | 1971-11-16 | 1973-05-24 | Bayer Ag | Pyrimido eckige klammer auf 4,5-d eckige klammer zu pyrimidine |
US3894021A (en) | 1974-01-28 | 1975-07-08 | Squibb & Sons Inc | Derivatives of 1,7-dihydro-2H-pyrazolo{8 4{40 ,3{40 :5,6{9 pyrido{8 4,3-D{9 pyrimidine-2,4-(3H)-diones |
JPS5120580B2 (hr) | 1974-06-19 | 1976-06-25 | ||
JPS5120580A (en) | 1974-08-08 | 1976-02-18 | Nitto Electric Ind Co | 4 futsukaechirenjugotaihifukudensenno seizohoho |
US4347348A (en) | 1978-06-05 | 1982-08-31 | Chernikhov Alexei Y | Heat-resistant heterocyclic polymers and methods for producing same |
FR2428654A1 (fr) | 1978-06-13 | 1980-01-11 | Chernikhov Alexei | Polymeres heterocycliques thermostables et leurs procedes de preparation |
CH641470A5 (de) | 1978-08-30 | 1984-02-29 | Ciba Geigy Ag | Imidgruppen enthaltende silane. |
CH635828A5 (de) | 1978-08-30 | 1983-04-29 | Ciba Geigy Ag | N-substituierte imide und bisimide. |
US4339267A (en) | 1980-01-18 | 1982-07-13 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
US4405519A (en) | 1980-10-22 | 1983-09-20 | Plastics Engineering Company | Di-Acetylene-terminated polyimide derivatives |
US4402878A (en) | 1980-10-22 | 1983-09-06 | Plastics Engineering Company | Addition products of di-acetylene-terminated polyimide derivatives with a polyimide having terminal non-conjugated acetylene groups |
US4405786A (en) | 1980-10-22 | 1983-09-20 | Plastics Engineering Company | Addition products of di-acetylene-terminated polyimide derivatives and an dienophile having ethylene groups |
US4405520A (en) | 1980-10-22 | 1983-09-20 | Plastics Engineering Company | Addition products of di-acetylene-terminated polymide derivatives and dienophiles having terminal maleimide grops |
JPS5857170A (ja) | 1981-09-30 | 1983-04-05 | シャープ株式会社 | 学習機 |
JPS5873576U (ja) | 1981-11-12 | 1983-05-18 | 沖電気工業株式会社 | コネクタのロツク構造 |
US4460773A (en) | 1982-02-05 | 1984-07-17 | Lion Corporation | 1-Phenyl-1H-pyrazolo [3,4-b]pyrazine derivatives and process for preparing same |
JPS5926040U (ja) | 1982-08-12 | 1984-02-17 | 井出 正一 | ロ−プ掛締付け器 |
DE3432983A1 (de) | 1983-09-07 | 1985-04-18 | Lion Corp., Tokio/Tokyo | 1,5-disubstituierte 1h-pyrazolo(3,4-b)-pyrazin-derivate und antitumormittel, die diese enthalten |
JPH029895Y2 (hr) | 1984-11-08 | 1990-03-12 | ||
JPH0348656Y2 (hr) | 1985-05-10 | 1991-10-17 | ||
JPS62273979A (ja) | 1986-05-21 | 1987-11-28 | Lion Corp | 1,5−置換−1H−ピラゾロ〔3,4−b〕ピラジン誘導体及び該化合物を含有する抗腫瘍剤 |
JPS6310630A (ja) | 1986-06-23 | 1988-01-18 | Teijin Ltd | 芳香族ポリアミドイミドエ−テルの製造法 |
JPS6317882A (ja) | 1986-07-09 | 1988-01-25 | Lion Corp | 5−置換−1H−ピラゾロ〔3,4−b〕ピラジン誘導体及び該化合物を含有する抗腫瘍剤 |
US4859672A (en) | 1986-10-29 | 1989-08-22 | Rorer Pharmaceutical Corporation | Pyrido[2,3-d]pyrimidinone and imidazo[4,5-b]pyrimidinone |
US4874803A (en) | 1987-09-21 | 1989-10-17 | Pennwalt Corporation | Dianhydride coupled polymer stabilizers |
DE3814549A1 (de) | 1987-10-30 | 1989-05-18 | Bayer Ag | N-substituierte derivate von 1-desoxynojirimycin und 1-desoxymannonojirimycin, verfahren zu deren herstellung und deren verwendung in arzneimitteln |
JPH029895A (ja) | 1988-06-28 | 1990-01-12 | Lion Corp | ヌクレオシド類似化合物及び抗腫瘍剤 |
DD280853A1 (de) | 1989-03-21 | 1990-07-18 | Akad Nauk Sssr | Bindemittel fuer elektroden, vorzugsweise fuer polymerelektroden |
US5159054A (en) | 1989-05-16 | 1992-10-27 | The United States Of America As Represented By The Secretary Of The Navy | Synthesis of phthalonitrile resins containing ether and imide linkages |
JP2845957B2 (ja) | 1989-07-17 | 1999-01-13 | 三井化学株式会社 | イミド環を有する新規ジフェノール類およびその製造方法 |
US5726302A (en) | 1989-09-15 | 1998-03-10 | Gensia Inc. | Water soluble adenosine kinase inhibitors |
DE3937633A1 (de) | 1989-11-11 | 1991-05-16 | Bayer Ag | Heterocyclische verbindungen und deren verwendung als pigmente und farbstoffe |
US5329046A (en) | 1989-12-28 | 1994-07-12 | Hoechst Aktiengesellschaft | Biscationic acid amide and imide derivatives and processes for their preparation |
EP0506867B1 (de) | 1989-12-28 | 1995-09-20 | Hoechst Aktiengesellschaft | Biskationische säureamid- und -imidderivate als ladungssteuermittel |
JP2883670B2 (ja) | 1990-03-23 | 1999-04-19 | 三井化学株式会社 | イミド環を有する新規ビスフェノール類およびその製造方法 |
GB9113137D0 (en) | 1990-07-13 | 1991-08-07 | Ici Plc | Thioxo heterocycles |
CA2093322C (en) | 1990-10-03 | 2002-01-29 | Jonathan H. Hodgkin | Epoxy resins based on diaminobisimide compounds |
JPH04158084A (ja) | 1990-10-22 | 1992-06-01 | Fuji Photo Film Co Ltd | 記録材料 |
JPH04179576A (ja) | 1990-11-14 | 1992-06-26 | Fuji Photo Film Co Ltd | 記録材料 |
JPH04328121A (ja) | 1991-04-26 | 1992-11-17 | Sumitomo Bakelite Co Ltd | 半導体封止用エポキシ樹脂組成物 |
AU657986B2 (en) | 1991-06-14 | 1995-03-30 | Pharmacia & Upjohn Company | Imidazo(1,5-a)quinoxalines |
DE4119767A1 (de) | 1991-06-15 | 1992-12-17 | Dresden Arzneimittel | Verfahren zur herstellung von (pyrimid-2-yl-thio- bzw. seleno)-essigsaeurederivaten |
US5521184A (en) | 1992-04-03 | 1996-05-28 | Ciba-Geigy Corporation | Pyrimidine derivatives and processes for the preparation thereof |
JP3279635B2 (ja) | 1992-05-18 | 2002-04-30 | 鐘淵化学工業株式会社 | ヒドロシリル基含有イミド化合物 |
JP3232123B2 (ja) | 1992-05-20 | 2001-11-26 | 鐘淵化学工業株式会社 | 硬化性組成物 |
JPH07506836A (ja) | 1992-05-28 | 1995-07-27 | コモンウェルス・サイエンティフィック・アンド・インダストリアル・リサーチ・オーガニゼイション | ビスマレイミド化合物 |
WO1994013669A1 (en) | 1992-12-07 | 1994-06-23 | Commonwealth Scientific And Industrial Research Organisation | Bisnadimides |
JPH08506189A (ja) | 1993-01-11 | 1996-07-02 | ザ・トラスティーズ・オブ・ザ・ユニバーシティ・オブ・ペンシルバニア | 非線形光学的性質を有する多環式芳香族化合物 |
WO1994025438A1 (en) | 1993-04-28 | 1994-11-10 | The Du Pont Merck Pharmaceutical Company | Novel trisubstituted aromatic amines useful for the treatment of cognitive deficits |
US5536725A (en) | 1993-08-25 | 1996-07-16 | Fmc Corporation | Insecticidal substituted-2,4-diamino-5,6,7,8-tetrahydroquinazolines |
RU2139281C1 (ru) | 1993-11-30 | 1999-10-10 | Джи Ди Сирл энд Компани | Пиразолилзамещенный бензолсульфонамид или его фармацевтически приемлемая соль, фармацевтическая композиция, способ лечения от воспаления или связанного с воспалением заболевания |
US5480887A (en) | 1994-02-02 | 1996-01-02 | Eli Lilly And Company | Protease inhibitors |
PT746320E (pt) | 1994-02-02 | 2001-05-31 | Lilly Co Eli | Intermediarios e inibidores da protease de hiv |
ATE190978T1 (de) | 1994-11-14 | 2000-04-15 | Warner Lambert Co | 6-aryl-pyrido(2,3-d)pyrimidine und -naphthyridine zur hemmung der durch protein-tyrosin-kinase hervorgerufenen zellvermehrung |
US7067664B1 (en) | 1995-06-06 | 2006-06-27 | Pfizer Inc. | Corticotropin releasing factor antagonists |
US5783577A (en) | 1995-09-15 | 1998-07-21 | Trega Biosciences, Inc. | Synthesis of quinazolinone libraries and derivatives thereof |
JPH09188812A (ja) | 1996-01-11 | 1997-07-22 | Mitsui Toatsu Chem Inc | 結晶化促進剤 |
JP3531169B2 (ja) | 1996-06-11 | 2004-05-24 | 三菱ウェルファーマ株式会社 | 縮合ヘテロ環化合物およびその医薬用途 |
SK14099A3 (en) | 1996-08-06 | 2000-05-16 | Pfizer | Substituted pyrido- or pyrimido-containing 6,6- or 6,7-bicyclic derivatives |
EP0927167A1 (en) | 1996-08-14 | 1999-07-07 | Warner-Lambert Company | 2-phenyl benzimidazole derivatives as mcp-1 antagonists |
JP3669783B2 (ja) | 1996-08-21 | 2005-07-13 | 三井化学株式会社 | 有機電界発光素子 |
US5994364A (en) | 1996-09-13 | 1999-11-30 | Schering Corporation | Tricyclic antitumor farnesyl protein transferase inhibitors |
AU6908398A (en) | 1996-10-28 | 1998-05-22 | Versicor Inc | Fused 2,4-pyrimidinedione combinatorial libraries and biologically active fused 2,4-pyramidinediones |
US6057329A (en) | 1996-12-23 | 2000-05-02 | Celltech Therapeutics Limited | Fused polycyclic 2-aminopyrimidine derivatives |
AU749750B2 (en) | 1997-02-05 | 2002-07-04 | Warner-Lambert Company | Pyrido {2,3-d} pyrimidines and 4-aminopyrimidines as inhibitors of cellular proliferation |
CA2285263C (en) | 1997-04-11 | 2009-03-10 | Abbott Laboratories | Furopyridine, thienopyridine, pyrrolopyridine and related pyrimidine, pyridazine and triazine compounds useful in controlling chemical synaptic transmission |
KR100425638B1 (ko) | 1997-05-28 | 2004-04-03 | 아벤티스 파마슈티칼스 인크. | 혈소판-유도된 성장 인자 및/또는 P56lck 티로신키나제를 억제하는 퀴놀린 및 퀴녹살린 화합물 |
GB9716231D0 (en) | 1997-07-31 | 1997-10-08 | Amersham Int Ltd | Base analogues |
CA2300478A1 (en) | 1997-08-11 | 1999-02-18 | Cor Therapeutics, Inc. | Selective factor xa inhibitors |
WO1999009030A1 (en) | 1997-08-20 | 1999-02-25 | Warner-Lambert Company | Naphthyridinones for inhibiting protein tyrosine kinase and cell cycle kinase mediated cellular proliferation |
US6465484B1 (en) | 1997-09-26 | 2002-10-15 | Merck & Co., Inc. | Angiogenesis inhibitors |
JPH11171865A (ja) | 1997-12-04 | 1999-06-29 | Yoshitomi Pharmaceut Ind Ltd | 縮合ヘテロ環化合物 |
EP1057812A4 (en) | 1998-02-20 | 2001-07-25 | Takeda Chemical Industries Ltd | AMINOGUANIDINE HYDRAZONE DERIVATIVES, PROCESSES FOR PRODUCING SAME, AND MEDICINAL PRODUCTS BASED ON SUCH DERIVATIVES |
AU9298798A (en) | 1998-05-15 | 1999-12-06 | Guilford Pharmaceuticals Inc. | Fused tricyclic compounds which inhibit parp activity |
US20040044012A1 (en) | 1998-05-26 | 2004-03-04 | Dobrusin Ellen Myra | Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation |
GEP20033093B (en) * | 1998-05-26 | 2003-10-27 | Warner Lambert Co | Bicyclic Pyrimidines and Bicyclic 3,4-Dihydropyrimidines as Inhibitors of Cellular Proliferation, Compositions Containing Them and Methods for Treating Cell Proliferative Disorders |
WO1999064400A1 (en) | 1998-06-12 | 1999-12-16 | Vertex Pharmaceuticals Incorporated | INHIBITORS OF p38 |
BR9912938B1 (pt) | 1998-08-11 | 2011-06-28 | derivados de isoquinolina, composição que os compreende, processo para preparação e uso dos mesmos. | |
JP2000123973A (ja) | 1998-10-09 | 2000-04-28 | Canon Inc | 有機発光素子 |
GB9823103D0 (en) | 1998-10-23 | 1998-12-16 | Pfizer Ltd | Pharmaceutically active compounds |
CN1150195C (zh) | 1998-10-23 | 2004-05-19 | 霍夫曼-拉罗奇有限公司 | 双环氮杂环 |
US6133031A (en) | 1999-08-19 | 2000-10-17 | Isis Pharmaceuticals Inc. | Antisense inhibition of focal adhesion kinase expression |
GB9905075D0 (en) | 1999-03-06 | 1999-04-28 | Zeneca Ltd | Chemical compounds |
DE19912638A1 (de) | 1999-03-20 | 2000-09-21 | Bayer Ag | Naphthylcarbonsäureamid-substituierte Sulfonamide |
DE19920790A1 (de) | 1999-05-06 | 2000-11-09 | Bayer Ag | Bis-Sulfonamide mit anti-HCMV-Wirkung |
PE20010306A1 (es) | 1999-07-02 | 2001-03-29 | Agouron Pharma | Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa |
JP4041624B2 (ja) | 1999-07-21 | 2008-01-30 | 三井化学株式会社 | 有機電界発光素子 |
BRPI0014271B1 (pt) | 1999-09-24 | 2021-06-22 | Janssen Pharmaceutica N.V. | Partícula consistindo em uma dispersão de sólidos, uso da dita partícula, dispersão de sólidos, forma de dosagem farmacêutica, bem como processos de preparação de dita partícula, dispersão e forma de dosagem |
DE19946289A1 (de) | 1999-09-28 | 2001-03-29 | Basf Ag | Benzodiazepin-Derivate, deren Herstellung und Anwendung |
WO2001029042A1 (en) | 1999-10-21 | 2001-04-26 | F. Hoffmann-La Roche Ag | Heteroalkylamino-substituted bicyclic nitrogen heterocycles as inhibitors of p38 protein kinase |
CN1156477C (zh) | 1999-10-21 | 2004-07-07 | 霍夫曼-拉罗奇有限公司 | 作为p38蛋白激酶的抑制剂的烷基氨基-取代的双环氮杂环类化合物 |
TWI271406B (en) | 1999-12-13 | 2007-01-21 | Eisai Co Ltd | Tricyclic condensed heterocyclic compounds, preparation method of the same and pharmaceuticals comprising the same |
EP1242382B1 (en) | 1999-12-29 | 2007-02-07 | Wyeth | Tricyclic protein kinase inhibitors |
ES2304992T3 (es) | 2000-01-24 | 2008-11-01 | Warner-Lambert Company Llc | Agentes antibacterianos de 3-aminoquinazolin-2,4-diona. |
SK10772002A3 (sk) | 2000-01-27 | 2004-01-08 | Warner-Lambert Company | Pyridopyrimidinónové deriváty na liečbu neurodegeneratívnych ochorení |
US7041675B2 (en) | 2000-02-01 | 2006-05-09 | Abbott Gmbh & Co. Kg | Heterocyclic compounds and their use as PARP inhibitors |
WO2001057037A1 (en) | 2000-02-04 | 2001-08-09 | Cor Therapeutics, Inc. | Platelet adp receptor inhibitors |
DE60110749T2 (de) | 2000-02-09 | 2006-02-02 | Novartis Ag | Pyridinderivative als angiogenese- und/oder vegf-rezeptor-tyrosinkinase-inhibitoren |
GB0004890D0 (en) | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
DE60112268T2 (de) | 2000-03-06 | 2006-05-24 | Astrazeneca Ab | Verwendung von quinazolinderivate als inhibitoren der angiogenese |
DE10012549A1 (de) | 2000-03-15 | 2001-09-20 | Bayer Ag | Arzneimittel gegen virale Erkrankungen |
JP2001265031A (ja) | 2000-03-15 | 2001-09-28 | Fuji Xerox Co Ltd | 電子写真感光体、プロセスカートリッジ、及び、電子写真装置 |
TWI310035B (en) | 2000-04-28 | 2009-05-21 | Acadia Pharm Inc | Muscarinic agonists |
JP2003532728A (ja) | 2000-05-05 | 2003-11-05 | コー セラピューティックス, インコーポレイテッド | ヘテロ二環式スルホンアミドおよび血小板adpレセプターインヒビターとしてのそれらの使用 |
AU2001268712A1 (en) | 2000-06-23 | 2002-01-08 | Bristol-Myers Squibb Company | 1 - (heteroaryl-phenyl) - condensed pyrazol derivatives as factor Xa inhibitors |
ES2225624T3 (es) | 2000-06-28 | 2005-03-16 | Smithkline Beecham Plc | Procedimiento de molienda por via humeda. |
US20050009876A1 (en) | 2000-07-31 | 2005-01-13 | Bhagwat Shripad S. | Indazole compounds, compositions thereof and methods of treatment therewith |
WO2002012442A2 (en) | 2000-08-07 | 2002-02-14 | Neurogen Corporation | Heterocyclic compounds as ligands of the gabaa receptor |
JP5049447B2 (ja) | 2000-08-14 | 2012-10-17 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | 置換ピラゾール |
JP2004531456A (ja) | 2000-09-06 | 2004-10-14 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | 置換ピラゾールを用いてアレルギーを治療する方法 |
GB0025782D0 (en) | 2000-10-20 | 2000-12-06 | Pfizer Ltd | Use of inhibitors |
EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
GB0100621D0 (en) | 2001-01-10 | 2001-02-21 | Vernalis Res Ltd | Chemical compounds VI |
GB0103926D0 (en) | 2001-02-17 | 2001-04-04 | Astrazeneca Ab | Chemical compounds |
AP1699A (en) | 2001-03-21 | 2006-12-26 | Warner Lambert Co | New spirotricyclic derivatives and their use as phosphodiesterase-7 inhibitors |
US6998408B2 (en) | 2001-03-23 | 2006-02-14 | Bristol-Myers Squibb Pharma Company | 6-5, 6-6, or 6-7 Heterobicycles as factor Xa inhibitors |
JP2002296731A (ja) | 2001-03-30 | 2002-10-09 | Fuji Photo Film Co Ltd | 熱現像カラー画像記録材料 |
KR20040007497A (ko) | 2001-04-16 | 2004-01-24 | 에자이 가부시키가이샤 | 신규 1h-인다졸 화합물 |
ATE402164T1 (de) | 2001-04-26 | 2008-08-15 | Eisai R&D Man Co Ltd | Stickstoffhaltige verbindung mit kondensiertem ring und pyrazolylgruppe als substituent und medizinische zusammensetzung davon |
PL366934A1 (en) | 2001-04-30 | 2005-02-07 | Glaxo Group Limited | Fused pyrimidines as antagonists of the corticotropin releasing factor (crf) |
WO2002094825A1 (fr) | 2001-05-22 | 2002-11-28 | Banyu Pharmaceutical Co., Ltd. | Nouveau derive de spiropiperidine |
US20030114448A1 (en) | 2001-05-31 | 2003-06-19 | Millennium Pharmaceuticals, Inc. | Inhibitors of factor Xa |
CA2446963A1 (en) | 2001-06-19 | 2002-12-27 | Warner-Lambert Company Llc | Quinazolinediones as antibacterial agents |
GB0115109D0 (en) | 2001-06-21 | 2001-08-15 | Aventis Pharma Ltd | Chemical compounds |
WO2003000187A2 (en) | 2001-06-21 | 2003-01-03 | Ariad Pharmaceuticals, Inc. | Novel pyrazolo-and pyrrolo-pyrimidines and uses thereof |
WO2003000690A1 (en) | 2001-06-25 | 2003-01-03 | Aventis Pharmaceuticals Inc. | Synthesis of heterocyclic compounds employing microwave technology |
US20040235867A1 (en) | 2001-07-24 | 2004-11-25 | Bilodeau Mark T. | Tyrosine kinase inhibitors |
PL367983A1 (en) | 2001-08-07 | 2005-03-21 | Banyu Pharmaceutical Co, Ltd. | Spiro compounds |
MXPA04002243A (es) | 2001-09-19 | 2004-06-29 | Aventis Pharma Sa | Compuestos quimicos. |
DE60213842T2 (de) | 2001-10-30 | 2007-09-06 | Novartis Ag | Staurosporin-derivate als hemmer der flt3-rezeptor-tyrosinkinase-wirkung |
HUP0402106A3 (en) | 2001-11-01 | 2009-07-28 | Janssen Pharmaceutica Nv | Heteroaryl amines as glycogen synthase kinase 3 beta inhibitors, process for their preparation and pharmaceutical compositions containing them |
CN1582284A (zh) | 2001-11-07 | 2005-02-16 | 霍夫曼-拉罗奇有限公司 | 氨基嘧啶类和吡啶类化合物 |
CA2466279A1 (en) | 2001-11-13 | 2003-05-22 | Dana-Farber Cancer Institute, Inc. | Agents that modulate immune cell activation and methods of use thereof |
GB0129476D0 (en) | 2001-12-10 | 2002-01-30 | Syngenta Participations Ag | Organic compounds |
KR20060111716A (ko) | 2002-01-22 | 2006-10-27 | 워너-램버트 캄파니 엘엘씨 | 2-(피리딘-2-일아미노)-피리도[2,3-d]피리미딘-7-온 |
DK1482924T3 (da) | 2002-03-05 | 2008-09-29 | Merck Frosst Canada Ltd | Cathepsin-cystein-protease-inhibotorer |
US6815519B2 (en) | 2002-03-22 | 2004-11-09 | Chung-Shan Institute Of Science & Technology | Acidic fluorine-containing poly (siloxane amideimide) silica hybrids |
BR0308937A (pt) | 2002-04-03 | 2005-01-04 | Hoffmann La Roche | Compostos imidazo fundidos |
UA80820C2 (en) | 2002-05-15 | 2007-11-12 | Janssen Pharmaceutica Nv | N-substituted tricyclic 3-aminopyrazoles as pdfg receptor inhibitors |
JP4499342B2 (ja) | 2002-05-16 | 2010-07-07 | 株式会社カネカ | SiH基を含有する含窒素有機系化合物の製造方法 |
US7034033B2 (en) | 2002-05-23 | 2006-04-25 | Chiron Corporation | Substituted quinazolinone compounds |
US7119111B2 (en) | 2002-05-29 | 2006-10-10 | Amgen, Inc. | 2-oxo-1,3,4-trihydroquinazolinyl derivatives and methods of use |
TW200406374A (en) | 2002-05-29 | 2004-05-01 | Novartis Ag | Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases |
US7105526B2 (en) | 2002-06-28 | 2006-09-12 | Banyu Pharmaceuticals Co., Ltd. | Benzimidazole derivatives |
GB0215676D0 (en) | 2002-07-05 | 2002-08-14 | Novartis Ag | Organic compounds |
PA8577501A1 (es) | 2002-07-25 | 2004-02-07 | Warner Lambert Co | Inhibidores de quinasas |
ATE451104T1 (de) | 2002-07-29 | 2009-12-15 | Rigel Pharmaceuticals Inc | Verfahren zur behandlung oder pruvention von autoimmunkrankheiten mit 2,4-pyrimidindiamin- verbindungen |
PL375403A1 (en) | 2002-08-06 | 2005-11-28 | F.Hoffmann-La Roche Ag | 6-alkoxy-pyrido-pyrimidines as p-38 map kinase inhibitors |
EP1388541A1 (en) | 2002-08-09 | 2004-02-11 | Centre National De La Recherche Scientifique (Cnrs) | Pyrrolopyrazines as kinase inhibitors |
US7084270B2 (en) | 2002-08-14 | 2006-08-01 | Hoffman-La Roche Inc. | Pyrimido compounds having antiproliferative activity |
GB0220187D0 (en) | 2002-08-30 | 2002-10-09 | Novartis Ag | Organic compounds |
GB0223349D0 (en) | 2002-10-08 | 2002-11-13 | Merck Sharp & Dohme | Therapeutic agents |
US7129351B2 (en) | 2002-11-04 | 2006-10-31 | Hoffmann-La Roche Inc. | Pyrimido compounds having antiproliferative activity |
TW200413381A (en) | 2002-11-04 | 2004-08-01 | Hoffmann La Roche | Novel amino-substituted dihydropyrimido [4,5-d]pyrimidinone derivatives, their manufacture and use as pharmaceutical agents |
US7384937B2 (en) | 2002-11-06 | 2008-06-10 | Bristol-Myers Squibb Co. | Fused heterocyclic compounds and use thereof |
CL2003002353A1 (es) | 2002-11-15 | 2005-02-04 | Vertex Pharma | Compuestos derivados de diaminotriazoles, inhibidores d ela proteina quinasa; composicion farmaceutica; procedimiento de preparacion; y su uso del compuesto en el tratamiento de enfermedades de desordenes alergicos, proliferacion, autoinmunes, condic |
CN100357293C (zh) * | 2002-11-18 | 2007-12-26 | 霍夫曼-拉罗奇有限公司 | 二嗪并嘧啶类 |
US7504410B2 (en) | 2002-11-28 | 2009-03-17 | Schering Aktiengesellschaft | Chk-, Pdk- and Akt-inhibitory pyrimidines, their production and use as pharmaceutical agents |
JP4903385B2 (ja) | 2002-12-06 | 2012-03-28 | パーデュー・リサーチ・ファウンデーション | 損傷した哺乳類神経組織を治療するためのピリジン類 |
US7759336B2 (en) | 2002-12-10 | 2010-07-20 | Ono Pharmaceutical Co., Ltd. | Nitrogen-containing heterocyclic compounds and medicinal use thereof |
UA80171C2 (en) | 2002-12-19 | 2007-08-27 | Pfizer Prod Inc | Pyrrolopyrimidine derivatives |
US7098332B2 (en) | 2002-12-20 | 2006-08-29 | Hoffmann-La Roche Inc. | 5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones |
UA80767C2 (en) | 2002-12-20 | 2007-10-25 | Pfizer Prod Inc | Pyrimidine derivatives for the treatment of abnormal cell growth |
CA2508660C (en) | 2002-12-23 | 2013-08-20 | Wyeth | Antibodies against pd-1 and uses therefor |
JP2004203749A (ja) | 2002-12-24 | 2004-07-22 | Kanegafuchi Chem Ind Co Ltd | SiH基を含有する含窒素有機系化合物の製造方法 |
BRPI0406809A (pt) | 2003-01-17 | 2005-12-27 | Warner Lambert Co | Heterociclos substituìdos de 2-aminopiridina como inibidores da proliferação celular |
GB0305929D0 (en) | 2003-03-14 | 2003-04-23 | Novartis Ag | Organic compounds |
US7135469B2 (en) | 2003-03-18 | 2006-11-14 | Bristol Myers Squibb, Co. | Linear chain substituted monocyclic and bicyclic derivatives as factor Xa inhibitors |
US7687625B2 (en) | 2003-03-25 | 2010-03-30 | Takeda Pharmaceutical Company Limited | Dipeptidyl peptidase inhibitors |
GB0308208D0 (en) | 2003-04-09 | 2003-05-14 | Glaxo Group Ltd | Chemical compounds |
RU2350617C2 (ru) * | 2003-04-10 | 2009-03-27 | Ф.Хоффманн-Ля Рош Аг | Пиримидиновые соединения, обладающие свойствами селективного ингибирования активности кдр и фрфр |
RU2328497C2 (ru) | 2003-05-05 | 2008-07-10 | Ф.Хоффманн-Ля Рош Аг | Конденсированные производные пиримидина и лекарственное средство, обладающее активностью в отношении crf |
JP2004346145A (ja) | 2003-05-21 | 2004-12-09 | Teijin Ltd | イミド組成物およびそれからなる樹脂組成物、及びその製造方法 |
EP1651229A1 (en) | 2003-05-23 | 2006-05-03 | Chiron Corporation | Guanidino-substituted quinazolinone compounds as mc4-r agonists |
NZ543636A (en) | 2003-06-06 | 2009-07-31 | Arexis Ab | Use of fused heterocyclic compounds as SCCE inhibitors for the treatment of skin conditions or cancer |
IL156495A0 (en) | 2003-06-17 | 2004-01-04 | Prochon Biotech Ltd | Use of fgfr3 antagonists for treating t cell mediated diseases |
US20060270849A1 (en) | 2003-06-18 | 2006-11-30 | Shigeyoshi Nishino | Process for producing pyrimidin-4-one compound |
JP2005015395A (ja) | 2003-06-26 | 2005-01-20 | Japan Science & Technology Agency | 新規ピリミドピリミジンヌクレオシドとその構造類縁体 |
CN1984660B (zh) | 2003-07-03 | 2010-12-15 | 美瑞德生物工程公司 | 作为天冬氨酸特异性半胱氨酸蛋白酶活化剂和细胞程序死亡诱导剂的4-芳基氨基-喹唑啉 |
AR045037A1 (es) | 2003-07-10 | 2005-10-12 | Aventis Pharma Sa | Tetrahidro-1h-pirazolo [3,4-c] piridinas sustituidas, composiciones que las contienen y su utilizacion. |
BRPI0413005A (pt) | 2003-07-29 | 2006-09-26 | Irm Llc | compostos e composições como inibidores da proteìna cinase |
US7390820B2 (en) | 2003-08-25 | 2008-06-24 | Amgen Inc. | Substituted quinolinone derivatives and methods of use |
JP2007504243A (ja) | 2003-09-03 | 2007-03-01 | ニューロジェン・コーポレーション | 5−アリール−ピラゾロ[4,3−d]ピリミジン類、ピリジン類、ピラジン類及び関連化合物 |
CA2539548A1 (en) | 2003-09-18 | 2005-03-31 | Conforma Therapeutics Corporation | Novel heterocyclic compounds as hsp90-inhibitors |
CA2537325A1 (en) | 2003-09-19 | 2005-03-31 | Gilead Sciences, Inc. | Aza-quinolinol phosphonate integrase inhibitor compounds |
PE20050952A1 (es) | 2003-09-24 | 2005-12-19 | Novartis Ag | Derivados de isoquinolina como inhibidores de b-raf |
DE602004032276D1 (de) | 2003-10-01 | 2011-05-26 | Xention Ltd | Tetrahydro-Naphthalen und Harnstoffderivate |
BRPI0415210A (pt) | 2003-10-08 | 2006-12-05 | Irm Llc | compostos e composições como inibidores de proteìna cinase |
CN1897950A (zh) | 2003-10-14 | 2007-01-17 | 惠氏公司 | 稠合芳基和杂芳基衍生物及其使用方法 |
US20090099165A1 (en) | 2003-10-14 | 2009-04-16 | Arizona Board Of Regents On Behalf Of The University Of Arizona | Protein Kinase Inhibitors |
WO2005047289A1 (en) | 2003-11-17 | 2005-05-26 | Pfizer Products Inc. | Pyrrolopyrimidine compounds useful in treatment of cancer |
WO2005056524A2 (en) | 2003-12-09 | 2005-06-23 | Euro-Celtique S.A. | Therapeutic agents useful for treating pain |
US20080188527A1 (en) | 2003-12-23 | 2008-08-07 | Cashman John R | Synthetic Compounds and Derivatives as Modulators of Smoking or Nicotine Ingestion and Lung Cancer |
KR100703068B1 (ko) | 2003-12-30 | 2007-04-05 | 에스케이케미칼주식회사 | 피리딘 유도체와 이의 제조방법, 및 이를 포함하는약제조성물 |
US20050222171A1 (en) | 2004-01-22 | 2005-10-06 | Guido Bold | Organic compounds |
JP2007524673A (ja) | 2004-01-23 | 2007-08-30 | アムジエン・インコーポレーテツド | バニロイド受容体リガンドと治療におけるその使用 |
JP4879755B2 (ja) | 2004-01-23 | 2012-02-22 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | キノリン誘導体及びマイコバクテリア抑制剤としてのその使用 |
EP1715855A4 (en) | 2004-01-29 | 2010-06-16 | Elixir Pharmaceuticals Inc | ANTIVIRAL DRUGS |
GB0402137D0 (en) | 2004-01-30 | 2004-03-03 | Smithkline Beecham Corp | Novel compounds |
BRPI0507668A (pt) | 2004-02-14 | 2007-07-17 | Irm Llc | compostos e composições como inibidores de proteìna cinase |
WO2005082903A1 (en) | 2004-02-18 | 2005-09-09 | Warner-Lambert Company Llc | 2-(pyridin-3-ylamino)-pyrido[2,3-d]pyrimidin-7-ones |
AU2005219525B2 (en) | 2004-02-27 | 2011-08-18 | F. Hoffmann-La Roche Ag | Fused derivatives of pyrazole |
CA2558109A1 (en) | 2004-02-27 | 2005-09-15 | F. Hoffmann-La Roche Ag | Heteroaryl-fused pyrazolo derivatives |
US20080004263A1 (en) | 2004-03-04 | 2008-01-03 | Santora Vincent J | Ligands of Follicle Stimulating Hormone Receptor and Methods of Use Thereof |
US20070197510A1 (en) | 2004-03-10 | 2007-08-23 | Kazuyuki Ohmoto | Nitriles and medicinal compositions containing the same as the active ingredient |
US7763727B2 (en) | 2004-03-29 | 2010-07-27 | Mitsui Chemicals, Inc. | Compound and organic electronic device using the same |
WO2005105097A2 (en) | 2004-04-28 | 2005-11-10 | Gpc Biotech Ag | Pyridopyrimidines for treating inflammatory and other diseases |
JP2005320288A (ja) | 2004-05-10 | 2005-11-17 | Mitsui Chemicals Inc | テトラカルボン酸誘導体、および該化合物を用いた電子写真感光体、電子写真装置 |
US20050256309A1 (en) | 2004-05-12 | 2005-11-17 | Altenbach Robert J | Tri-and bi-cyclic heteroaryl histamine-3 receptor ligands |
MXPA06013805A (es) | 2004-05-27 | 2007-02-02 | Pfizer Prod Inc | Derivados de pirrolopirimidina de utilidad en el tratamiento contra el cancer. |
PE20060426A1 (es) | 2004-06-02 | 2006-06-28 | Schering Corp | DERIVADOS DE ACIDO TARTARICO COMO INHIBIDORES DE MMPs, ADAMs, TACE Y TNF-alfa |
ES2396135T3 (es) | 2004-06-10 | 2013-02-19 | Irm Llc | Compuestos y composiciones como inhibidores de proteínas cinasas |
ATE383360T1 (de) | 2004-06-11 | 2008-01-15 | Japan Tobacco Inc | 5-amino-2,4,7-trioxo-3,4,7,8-tetrahydro-2h- pyrido(2,3-d)pyrimidinderivate und verwandte verbindungen zur behandlung von krebs |
GB0512324D0 (en) | 2005-06-16 | 2005-07-27 | Novartis Ag | Organic compounds |
JP2006028027A (ja) | 2004-07-12 | 2006-02-02 | Mitsui Chemicals Inc | テトラカルボン酸誘導体、および該化合物を用いた電子写真感光体、電子写真装置 |
EP1789399A1 (en) | 2004-08-31 | 2007-05-30 | AstraZeneca AB | Quinazolinone derivatives and their use as b-raf inhibitors |
AU2005279337A1 (en) | 2004-08-31 | 2006-03-09 | F. Hoffmann-La Roche Ag | Amide derivatives of 7-amino-3-phenyl-dihydropyrimido [4,5-d]pyrimidinones, their manufacture and use as pharmaceutical agents |
MX2007002096A (es) | 2004-08-31 | 2007-03-29 | Hoffmann La Roche | Derivados de amida de 3-fenil-dihidropirimido[4,5-d] pirimidinonas, su fabricacion y su uso como agentes farmaceuticos. |
DE102004042667A1 (de) | 2004-09-01 | 2006-03-30 | Ewald Dörken Ag | Mehrschichtige Gebäudewand |
WO2006028289A1 (en) | 2004-09-10 | 2006-03-16 | Ube Industries, Ltd. | Modified polyimide resin and curable resin composition |
WO2007053135A1 (en) | 2004-09-14 | 2007-05-10 | Minerva Biotechnologies Corporation | Methods for diagnosis and treatment of cancer |
GB0420719D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
WO2006038112A1 (en) | 2004-10-01 | 2006-04-13 | Warner-Lambert Company Llc | Use of kinase inhibitors to promote neochondrogenesis |
FR2876582B1 (fr) | 2004-10-15 | 2007-01-05 | Centre Nat Rech Scient Cnrse | Utilisation de derives de pyrrolo-pyrazines pour la fabrication de medicaments pour le traitement de la mucoviscidose et de maladies liees a un defaut d'adressage des proteines dans les cellules |
US20060135553A1 (en) | 2004-10-28 | 2006-06-22 | Campbell David A | Imidazole derivatives |
WO2006050076A1 (en) | 2004-10-29 | 2006-05-11 | Janssen Pharmaceutica, N.V. | Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders |
AU2005304952B2 (en) | 2004-11-08 | 2013-04-04 | Baxter Healthcare S.A. | Nanoparticulate compositions of tubulin inhibitors |
KR20070097441A (ko) | 2004-11-18 | 2007-10-04 | 인사이트 산 디에고 인코포레이티드 | 11-β 하이드록실 스테로이드 데하이드로게나제 유형 1의억제제 및 이를 사용하는 방법 |
US20060122185A1 (en) | 2004-11-22 | 2006-06-08 | Jeremy Green | Bicyclic inhibitors of Rho kinase |
JP2008520612A (ja) | 2004-11-24 | 2008-06-19 | ノバルティス アクチエンゲゼルシャフト | JAK阻害剤およびBcr−Abl、Flt−3、FAKまたはRAFキナーゼ阻害剤のうち少なくとも1個の組合せ |
MY140748A (en) | 2004-12-06 | 2010-01-15 | Astrazeneca Ab | Novel pyrrolo [3,2-d] pyrimidin-4-one derivatives and their use in therapy |
WO2006065703A1 (en) | 2004-12-13 | 2006-06-22 | Sunesis Pharmaceuticals, Inc. | Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors |
WO2006074293A2 (en) | 2005-01-07 | 2006-07-13 | President And Fellows Of Harvard College | Bicyclic dihydropyrimidines as eg5 inhibitors |
DE102005008310A1 (de) | 2005-02-17 | 2006-08-24 | Schering Ag | Verwendung von CDKII Inhibitoren zur Fertilitätskontrolle |
BRPI0607402A2 (pt) | 2005-03-01 | 2009-09-01 | Pfizer Ltd | uso de inibidores de pde7 para o tratamento de dor neuropática |
US7402596B2 (en) | 2005-03-24 | 2008-07-22 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
JP2008543276A (ja) | 2005-03-30 | 2008-12-04 | ミネルバ バイオテクノロジーズ コーポレーション | Muc1発現細胞の増殖 |
JP2006284843A (ja) | 2005-03-31 | 2006-10-19 | Mitsui Chemicals Inc | テトラカルボン酸誘導体を用いた電子写真感光体、電子写真装置 |
US20060223993A1 (en) | 2005-04-01 | 2006-10-05 | Connor Daniel M | Colorant compounds, intermediates, and compositions |
JP2006316054A (ja) | 2005-04-15 | 2006-11-24 | Tanabe Seiyaku Co Ltd | 高コンダクタンス型カルシウム感受性kチャネル開口薬 |
KR100781704B1 (ko) | 2005-04-20 | 2007-12-03 | 에스케이케미칼주식회사 | 피리딘 유도체와 이의 제조방법, 및 이를 포함하는약제조성물 |
WO2006119504A2 (en) | 2005-05-04 | 2006-11-09 | Renovis, Inc. | Fused heterocyclic compounds, and compositions and uses thereof |
EP2161336B2 (en) | 2005-05-09 | 2017-03-29 | ONO Pharmaceutical Co., Ltd. | Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics |
WO2006124731A2 (en) | 2005-05-12 | 2006-11-23 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
ES2358344T3 (es) | 2005-05-13 | 2011-05-09 | Irm, Llc | Compuestos y composiciones como inhibidores de proteína quinasa. |
WO2006135821A2 (en) | 2005-06-09 | 2006-12-21 | Achille Carlisle Tisdelle | Vehicular head and neck safety system and method |
GB0512844D0 (en) | 2005-06-23 | 2005-08-03 | Novartis Ag | Organic compounds |
PT1907424E (pt) | 2005-07-01 | 2015-10-09 | Squibb & Sons Llc | Anticorpos monoclonais humanos para o ligando 1 de morte programada (pd-l1) |
WO2007013964A1 (en) | 2005-07-22 | 2007-02-01 | Sunesis Pharmaceuticals, Inc. | Pyrazolo pyrimidines useful as aurora kinase inhibitors |
WO2007013673A1 (en) | 2005-07-29 | 2007-02-01 | Astellas Pharma Inc. | Fused heterocycles as lck inhibitors |
ES2270715B1 (es) | 2005-07-29 | 2008-04-01 | Laboratorios Almirall S.A. | Nuevos derivados de pirazina. |
BRPI0614804A2 (pt) | 2005-08-09 | 2011-04-12 | Irm Llc | compostos e composições como inibidores de proteìna cinase |
US7589101B2 (en) | 2005-08-16 | 2009-09-15 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
MX2008002383A (es) | 2005-08-25 | 2008-03-18 | Hoffmann La Roche | Pirazol fusionado como inhibidores de proteinas cinasas activadas por mitogenos p38. |
US7678917B2 (en) | 2005-09-01 | 2010-03-16 | Hoffman-La Roche Inc. | Factor Xa inhibitors |
EA200800549A1 (ru) | 2005-09-06 | 2008-08-29 | Смитклайн Бичем Корпорейшн | Региоселективный способ получения бензимидазолтиофенов |
AU2006289838B2 (en) | 2005-09-15 | 2011-08-18 | Aska Pharmaceutical Co., Ltd. | Heterocyclic compound, and production process and use thereof |
US20070116984A1 (en) | 2005-09-21 | 2007-05-24 | Doosan Corporation | Spiro-compound for electroluminescent display device and electroluminescent display device comprising the same |
JP2009508966A (ja) | 2005-09-23 | 2009-03-05 | シェーリング コーポレイション | 治療薬としての縮合四環性mGluR1アンタゴニスト |
DE102005048072A1 (de) | 2005-09-24 | 2007-04-05 | Bayer Cropscience Ag | Thiazole als Fungizide |
AU2006302179C1 (en) | 2005-10-07 | 2013-06-20 | Exelixis, Inc. | N- (3-amino-quinoxalin-2-yl) -sulfonamide derivatives and their use as phosphatidylinositol 3-kinase inhibitors |
WO2007044698A1 (en) | 2005-10-07 | 2007-04-19 | Exelixis, Inc. | PYRIDOPYRIMIDINONE INHIBITORS OF PI3Kα |
WO2007061554A2 (en) | 2005-10-21 | 2007-05-31 | Purdue Research Foundation | Dosage of 4-aminopyridine derivatives for treatment of central nervous system injuries |
AU2006307953A1 (en) | 2005-10-26 | 2007-05-03 | Boehringer Ingelheim International Gmbh | (Hetero)aryl compounds with MCH antagonistic activity and medicaments comprising these compounds |
MY167260A (en) | 2005-11-01 | 2018-08-14 | Targegen Inc | Bi-aryl meta-pyrimidine inhibitors of kinases |
WO2007053498A1 (en) | 2005-11-01 | 2007-05-10 | Millennium Pharmaceuticals, Inc. | Compounds useful as antagonists of ccr2 |
US8604042B2 (en) | 2005-11-01 | 2013-12-10 | Targegen, Inc. | Bi-aryl meta-pyrimidine inhibitors of kinases |
WO2007056023A2 (en) | 2005-11-02 | 2007-05-18 | Targegen, Inc. | Thiazole inhibitors targeting resistant kinase mutations |
ES2401099T3 (es) | 2005-11-02 | 2013-04-16 | Bayer Intellectual Property Gmbh | Pirrolo[2,1-F] [1,2,4]-triazin-4-ilaminas como inhibidores de la quinasa IGF-1R para el tratamiento del cáncer y de otras enfermedades hiperproliferativas |
EP1953165B1 (en) | 2005-11-10 | 2012-02-01 | Msd K.K. | Aza-substituted spiro derivative |
DE602006018057D1 (de) | 2005-11-10 | 2010-12-16 | Chemocentryx Inc | Substituierte chinolone und verwendungsverfahren |
WO2007058626A1 (en) | 2005-11-16 | 2007-05-24 | S*Bio Pte Ltd | Indazole compounds |
AR057986A1 (es) | 2005-11-21 | 2008-01-09 | Japan Tobacco Inc | Compuesto heterociclico y su uso farmaceutico |
BRPI0619146A2 (pt) | 2005-12-02 | 2011-09-13 | Bayer Pharmaceuticals Corp | derivados de 4-amino-pirroltriazina substituìda úteis no tratamento de disordens e doenças hiperproliferativas associadas com angiogênesis |
PE20070855A1 (es) | 2005-12-02 | 2007-10-14 | Bayer Pharmaceuticals Corp | Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas |
US8110687B2 (en) | 2005-12-08 | 2012-02-07 | Millennium Pharmaceuticals, Inc. | Bicyclic compounds with kinase inhibitory activity |
WO2007066189A2 (en) | 2005-12-09 | 2007-06-14 | Pfizer Products Inc. | Salts, prodrugs and formulations of 1-[5-(4-amino-7-isopropyl-7h-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-2-methoxy-phenyl]-3-(2,4-dichloro-phenyl)-urea |
EP1968950A4 (en) | 2005-12-19 | 2010-04-28 | Genentech Inc | PYRIMIDINKINASEINHIBITOREN |
MEP3808A (xx) | 2005-12-21 | 2010-02-10 | Novartis Ag | Derivati pirimidinil aril uree kao fgf inhibitori |
US7998959B2 (en) | 2006-01-12 | 2011-08-16 | Incyte Corporation | Modulators of 11-β hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same |
UY30118A1 (es) | 2006-01-31 | 2007-06-29 | Tanabe Seiyaku Co | Compueto amina trisustituido |
US7427625B2 (en) | 2006-02-08 | 2008-09-23 | Janssen Pharmaceutica, N.V. | Substituted thiatriazaacenaphthylene-6-carbonitrile kinase inhibitors |
JP2009528989A (ja) | 2006-02-17 | 2009-08-13 | ファイザー・リミテッド | Tlr7変調剤としての3−デアザプリン誘導体 |
WO2007109334A2 (en) | 2006-03-21 | 2007-09-27 | Epix Delaware, Inc. | Sip receptor modulating compounds and use thereof |
WO2008117269A2 (en) | 2007-03-28 | 2008-10-02 | Atir Holding S.A. | Heterotri cyciii c compounds as serotonergic and/or dopaminergic agents and uses thereof |
EP2233472B1 (en) | 2006-03-28 | 2014-01-15 | Atir Holding S.A. | Heterocyclic compounds and uses thereof in the treatment of sexual disorders |
WO2007112347A1 (en) | 2006-03-28 | 2007-10-04 | Takeda Pharmaceutical Company Limited | Dipeptidyl peptidase inhibitors |
BRPI0709699A2 (pt) | 2006-03-29 | 2011-07-26 | Foldrx Pharmaceuticals Inc | inibiÇço da toxidez da alfa-sinucleina |
JP2010505739A (ja) | 2006-04-06 | 2010-02-25 | ウイスコンシン アラムニ リサーチ ファンデーション | 2−メチレン−1α,25−ジヒドロキシ−19,21−ジノルビタミンD3類縁体およびその使用 |
CN101472926A (zh) | 2006-04-13 | 2009-07-01 | 阿斯利康(瑞典)有限公司 | 硫代黄嘌呤衍生物以及它们作为髓过氧化物酶抑制剂的用途 |
GB0608386D0 (en) | 2006-04-27 | 2006-06-07 | Senexis Ltd | Compounds |
US7998978B2 (en) | 2006-05-01 | 2011-08-16 | Pfizer Inc. | Substituted 2-amino-fused heterocyclic compounds |
PL2027123T3 (pl) | 2006-05-11 | 2011-09-30 | Irm Llc | Związki i kompozycje jako inhibitory kinaz białkowych |
KR20080109095A (ko) * | 2006-05-15 | 2008-12-16 | 아이알엠 엘엘씨 | Fgf 수용체 키나제 억제제를 위한 조성물 및 방법 |
WO2007143600A2 (en) | 2006-06-05 | 2007-12-13 | Incyte Corporation | Sheddase inhibitors combined with cd30-binding immunotherapeutics for the treatment of cd30 positive diseases |
DE102006027156A1 (de) | 2006-06-08 | 2007-12-13 | Bayer Schering Pharma Ag | Sulfimide als Proteinkinaseinhibitoren |
MX2008015140A (es) | 2006-06-16 | 2008-12-10 | Albemarle Corp | Metodos para reducir o eliminar la salmonela en reptiles y/o sus huevos. |
ES2474865T3 (es) | 2006-06-22 | 2014-07-09 | Prana Biotechnology Limited | Método de tratamiento de un tumor cerebral glioma |
TW200817391A (en) | 2006-06-30 | 2008-04-16 | Astrazeneca Ab | Novel compounds |
WO2008005877A2 (en) | 2006-06-30 | 2008-01-10 | Board Of Regents, The University Of Texas System | Inhibitors of c-kit and uses thereof |
JP2009542604A (ja) | 2006-07-06 | 2009-12-03 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 4−ヘテロシクロアルキルピリミジン、それらの調製方法及び医薬としての使用 |
WO2008008234A1 (en) | 2006-07-07 | 2008-01-17 | Targegen, Inc. | 2-amino-5-substituted pyrimidine inhibitors |
TW200811134A (en) | 2006-07-12 | 2008-03-01 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
WO2008012635A2 (en) | 2006-07-26 | 2008-01-31 | Pfizer Products Inc. | Amine derivatives useful as anticancer agents |
EP2049481A2 (en) | 2006-08-09 | 2009-04-22 | SmithKline Beecham Corporation | Novel compounds as antagonists or inverse agonists for opioid receptors |
JP2010500994A (ja) | 2006-08-16 | 2010-01-14 | エグゼリクシス, インコーポレイテッド | Pi3kおよびmekモジュレーターを使用する方法 |
DE102006041382A1 (de) | 2006-08-29 | 2008-03-20 | Bayer Schering Pharma Ag | Carbamoyl-Sulfoximide als Proteinkinaseinhibitoren |
CA2974246C (en) | 2006-09-01 | 2020-02-25 | Senhwa Biosciences, Inc. | Tricyclic heteroaryl compounds and their use as protein modulators |
EP2063882A4 (en) | 2006-09-05 | 2010-03-03 | Univ Emory | TYROSINKINASE INHIBITOR FOR PREVENTING OR TREATING INFECTIONS |
EP2270200A3 (en) | 2006-09-11 | 2011-07-13 | CGI Pharmaceuticals, Inc. | Kinase inhibitors, and methods of using and identifying kinase inhibitors |
US7897762B2 (en) | 2006-09-14 | 2011-03-01 | Deciphera Pharmaceuticals, Llc | Kinase inhibitors useful for the treatment of proliferative diseases |
EP2074130A1 (en) | 2006-09-21 | 2009-07-01 | Boehringer Ingelheim International GmbH | Glucopyranosyl-substituted difluorobenzyl-benzene derivatives, medicaments containing such compounds, their use and process for their manufacture |
US20080176891A1 (en) | 2006-09-22 | 2008-07-24 | Paul Bamborough | Novel compounds |
CN101516888A (zh) | 2006-09-28 | 2009-08-26 | 诺瓦提斯公司 | 吡唑并[1,5-a]嘧啶衍生物及其治疗用途 |
US8202876B2 (en) | 2006-10-02 | 2012-06-19 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
JP2010508322A (ja) | 2006-10-30 | 2010-03-18 | グラクソ グループ リミテッド | システインプロテアーゼ阻害薬としての新規置換ピリジン誘導体 |
US7858645B2 (en) | 2006-11-01 | 2010-12-28 | Hoffmann-La Roche Inc. | Indazole derivatives |
EP2081928B1 (en) | 2006-11-10 | 2014-02-26 | Bristol-Myers Squibb Company | Pyrrolo-pyridine kinase inhibitors |
JP5380296B2 (ja) | 2006-11-17 | 2014-01-08 | ポリエラ コーポレイション | ジイミド系半導体材料ならびにジイミド系半導体材料を調製および使用する方法 |
US7892454B2 (en) | 2006-11-17 | 2011-02-22 | Polyera Corporation | Acene-based organic semiconductor materials and methods of preparing and using the same |
KR20080045536A (ko) | 2006-11-20 | 2008-05-23 | 에스케이케미칼주식회사 | 피리딘 화합물을 포함하는 간염 치료 및 예방 또는 간 보호효능을 갖는 약제 조성물 |
EP2104501B1 (en) | 2006-12-13 | 2014-03-12 | Merck Sharp & Dohme Corp. | Methods of cancer treatment with igf1r inhibitors |
WO2008071455A1 (en) | 2006-12-15 | 2008-06-19 | Bayer Schering Pharma Aktiengesellschaft | Bicyclic acyltryptophanols |
WO2008074068A1 (en) | 2006-12-20 | 2008-06-26 | Prana Biotechnology Limited | Substituted quinoline derivatives as antiamyloidogeneic agents |
US7737149B2 (en) | 2006-12-21 | 2010-06-15 | Astrazeneca Ab | N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]-4-(3,5-dimethylpiperazin-1-yl)benzamide and salts thereof |
CA2672172C (en) * | 2006-12-22 | 2016-05-03 | Astex Therapeutics Limited | Bicyclic heterocyclic compounds as fgfr inhibitors |
JP5442449B2 (ja) | 2006-12-22 | 2014-03-12 | アステックス、セラピューティックス、リミテッド | 新規化合物 |
EP2094682A2 (en) | 2006-12-22 | 2009-09-02 | Novartis AG | Heteroaryl-heteroaryl compounds as cdk inhibitors for the treatment of cancer, inflammation and viral infections |
FR2911140B1 (fr) | 2007-01-05 | 2009-02-20 | Sanofi Aventis Sa | Nouveaux derives de 2-anilino 4-heteroaryle pyrimides, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk |
US7893265B2 (en) | 2007-01-08 | 2011-02-22 | Polyera Corporation | Methods for preparing arene-BIS (dicarboximide)-based semiconducting materials and related intermediates for preparing same |
CN101007778A (zh) | 2007-01-10 | 2007-08-01 | 复旦大学 | 一种链延长型芴基双马来酰亚胺及其制备方法 |
CA2674589A1 (en) | 2007-01-12 | 2008-07-24 | Biocryst Pharmaceuticals, Inc. | Antiviral nucleoside analogs |
MX2009007426A (es) | 2007-01-12 | 2009-07-17 | Astellas Pharma Inc | Compuesto de piridina condensado. |
FR2911604B1 (fr) | 2007-01-19 | 2009-04-17 | Sanofi Aventis Sa | Derives de n-(heteroaryl-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique |
JP5358962B2 (ja) | 2007-02-06 | 2013-12-04 | 住友化学株式会社 | 組成物及び該組成物を用いてなる発光素子 |
JP2008198769A (ja) | 2007-02-13 | 2008-08-28 | Nippon Steel Chem Co Ltd | 有機エレクトロルミネッセント素子 |
EA200901167A1 (ru) | 2007-03-06 | 2010-04-30 | Новартис Аг | Бициклические органические соединения, пригодные для лечения воспалительных и аллергических состояний |
JP2010520293A (ja) | 2007-03-07 | 2010-06-10 | アラントス・フアーマシユーテイカルズ・ホールデイング・インコーポレイテツド | 複素環式部分を含有するメタロプロテアーゼ阻害剤 |
BRPI0808888B8 (pt) | 2007-03-12 | 2021-05-25 | Cytopia Res Pty Ltd | composto de fenil amino pirimidina para uso no tratamento de uma doença associada à quinase, processo para a preparação do composto, composição farmacêutica, e, implante |
US20080234262A1 (en) | 2007-03-21 | 2008-09-25 | Wyeth | Pyrazolopyrimidine analogs and their use as mtor kinase and pi3 kinase inhibitors |
WO2008118454A2 (en) | 2007-03-23 | 2008-10-02 | Amgen Inc. | Derivatives of quinoline or benzopyrazine and their uses for the treatment of (inter alia) inflammatory diseases, autoimmune diseases or various kinds of cancer |
KR20080091948A (ko) | 2007-04-10 | 2008-10-15 | 에스케이케미칼주식회사 | 락탐형 피리딘 화합물을 포함하는 허혈성 질환의 예방 및치료용 약학조성물 |
KR20100016477A (ko) | 2007-04-12 | 2010-02-12 | 어드밴스드 테크놀러지 머티리얼즈, 인코포레이티드 | Ald/cvd용의 지르코늄, 하프늄, 티타늄 및 규소 전구체 |
JP2010524941A (ja) | 2007-04-20 | 2010-07-22 | シェーリング コーポレイション | ピリミジノン誘導体およびそれらの使用方法 |
EP1985612A1 (en) | 2007-04-26 | 2008-10-29 | Bayer Schering Pharma Aktiengesellschaft | Arymethylen substituted N-Acyl-gamma-aminoalcohols |
US20100234386A1 (en) | 2007-05-10 | 2010-09-16 | Chaudhari Amita | Quinoxaline derivatives as pi3 kinase inhibitors |
EP1990342A1 (en) * | 2007-05-10 | 2008-11-12 | AEterna Zentaris GmbH | Pyridopyrazine Derivatives, Process of Manufacturing and Uses thereof |
WO2008144253A1 (en) | 2007-05-14 | 2008-11-27 | Irm Llc | Protein kinase inhibitors and methods for using thereof |
GB2449293A (en) | 2007-05-17 | 2008-11-19 | Evotec | Compounds having Hsp90 inhibitory activity |
AU2008259776A1 (en) | 2007-06-03 | 2008-12-11 | Vanderbilt University | Benzamide mGluR5 positive allosteric modulators and methods of making and using same |
EP2166842A4 (en) | 2007-06-07 | 2012-01-25 | Merck Sharp & Dohme | TRICYCLIC ANILIDHETEROCYCLES AS CGRP RECEPTOR ANTAGONISTS |
US8633186B2 (en) | 2007-06-08 | 2014-01-21 | Senomyx Inc. | Modulation of chemosensory receptors and ligands associated therewith |
US7928111B2 (en) | 2007-06-08 | 2011-04-19 | Senomyx, Inc. | Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors |
PT2168966T (pt) | 2007-06-15 | 2017-01-02 | Msd Kk | Derivado de bicicloanilina |
ES2616355T3 (es) | 2007-06-18 | 2017-06-12 | Merck Sharp & Dohme B.V. | Anticuerpos para el receptor humano de muerte programada PD-1 |
EP2018859A1 (en) | 2007-07-26 | 2009-01-28 | Bayer Schering Pharma Aktiengesellschaft | Arylmethylene substituted N-acyl-beta-amino alcohols |
WO2009013335A1 (en) | 2007-07-26 | 2009-01-29 | Novartis Ag | Organic compounds |
EP2020404A1 (en) | 2007-08-01 | 2009-02-04 | Bayer Schering Pharma Aktiengesellschaft | Cyanomethyl substituted N-Acyl Tryptamines |
WO2009019518A1 (en) | 2007-08-09 | 2009-02-12 | Astrazeneca Ab | Pyrimidine compounds having a fgfr inhibitory effect |
EP2173354A4 (en) | 2007-08-09 | 2011-10-05 | Glaxosmithkline Llc | CHINOXALIN DERIVATIVES AS PI3 KINASE INHIBITORS |
US9493419B2 (en) | 2007-08-21 | 2016-11-15 | The Hong Kong Polytechnic University | Quinoline derivatives as anti-cancer agents |
WO2009029625A1 (en) | 2007-08-27 | 2009-03-05 | Kalypsys, Inc. | 4- [heterocyclyl-methyl] -8-fluoro-quinolin-2-ones useful as nitric oxide synthase inhibitors |
US7960400B2 (en) | 2007-08-27 | 2011-06-14 | Duquesne University Of The Holy Ghost | Tricyclic compounds having cytostatic and/or cytotoxic activity and methods of use thereof |
US8530480B2 (en) | 2007-09-04 | 2013-09-10 | The Scripps Research Institute | Substituted pyrimidinyl-amines as protein kinase inhibitors |
WO2009030871A1 (en) | 2007-09-07 | 2009-03-12 | Vernalis R & D Ltd | Pyrrolopyrimidine derivatives having hsp90 inhibitory activity |
TW200920357A (en) | 2007-09-10 | 2009-05-16 | Curis Inc | HSP90 inhibitors containing a zinc binding moiety |
RU2501803C2 (ru) | 2007-10-01 | 2013-12-20 | Айзис Фармасьютикалз, Инк. | Композиции и способы модуляции экспрессии рецептора фактора роста фибробластов 4 (fgfr4) |
JP5470043B2 (ja) | 2007-10-05 | 2014-04-16 | Msd株式会社 | ベンゾオキサジノン誘導体 |
US20100298289A1 (en) | 2007-10-09 | 2010-11-25 | Ucb Pharma, S.A. | Heterobicyclic compounds as histamine h4-receptor antagonists |
WO2009049018A1 (en) | 2007-10-10 | 2009-04-16 | Syndax Pharmaceuticals, Inc. | Novel compounds and methods of using them |
CN101821243B (zh) | 2007-10-11 | 2013-05-08 | 中国科学院上海药物研究所 | 一类嘧啶取代苯丙酸衍生物及其作为ppar激动剂的用途 |
GB0720038D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New compounds |
GB0720041D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New Compounds |
WO2009047993A1 (ja) | 2007-10-13 | 2009-04-16 | Konica Minolta Holdings, Inc. | 有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
AU2008312631A1 (en) | 2007-10-16 | 2009-04-23 | Wyeth Llc | Thienopyrimidine and pyrazolopyrimidine compounds and their use as mTOR kinase and PI3 kinase inhibitors |
EP2212323B1 (en) | 2007-10-17 | 2012-08-15 | Novartis AG | Imidazo [1,2-a] pyridine derivatives useful as alk inhibitors |
EP2215085B1 (en) | 2007-10-25 | 2011-09-07 | AstraZeneca AB | Pyridine and pyrazine derivatives useful in the treatment of cell proliferative disorders |
RU2007139634A (ru) | 2007-10-25 | 2009-04-27 | Сергей Олегович Бачурин (RU) | Новые тиазол-, триазол- или оксадиазол-содержащие тетрациклические соединения |
WO2009056886A1 (en) | 2007-11-01 | 2009-05-07 | Astrazeneca Ab | Pyrimidine derivatives and their use as modulators of fgfr activity |
EP2222162B1 (en) | 2007-11-28 | 2016-11-16 | Dana-Farber Cancer Institute, Inc. | Small molecule myristate inhibitors of bcr-abl and methods of use |
WO2009071535A1 (en) | 2007-12-03 | 2009-06-11 | Boehringer Ingelheim International Gmbh | Diaminopyridines for the treatment of diseases which are characterised by excessive or anomal cell proliferation |
EA201001030A1 (ru) | 2007-12-19 | 2011-02-28 | Амген Инк. | Конденсированные соединения пиридина, пиримидина и триазина в качестве ингибиторов клеточного цикла |
CA2709784A1 (en) | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
CA2710458A1 (en) | 2007-12-21 | 2009-07-09 | Wyeth Llc | Imidazo [1,2-b] pyridazine compounds as modulators of liver x receptors |
WO2009086509A2 (en) | 2007-12-27 | 2009-07-09 | Purdue Research Foundation | Reagents for biomolecular labeling, detection and quantification employing raman spectroscopy |
FR2926297B1 (fr) | 2008-01-10 | 2013-03-08 | Centre Nat Rech Scient | Molecules chimiques inhibitrices du mecanisme d'epissage pour traiter des maladies resultant d'anomalies d'epissage. |
WO2009093210A2 (ru) | 2008-01-24 | 2009-07-30 | Alla Chem, Llc | ЗАМЕЩЕННЫЕ ЦИKЛOAЛKAHO[e ИЛИ d]ПИPAЗOЛO[l,5-a]ПИPИMИДИHЫ - АНТАГОНИСТЫ СЕРОТОНИНОВЫХ 5-HT6 РЕЦЕПТОРОВ, СПОСОБЫ ИХ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ |
EP2248816B1 (en) | 2008-01-24 | 2014-10-22 | Alla Chem, LLC. | 2-ALKYLAMINO-3-ARYLSULFONYL-CYCLOALCANO [e OR d] PYRAZOLO[1,5-A]PYRIMIDINES AS ANTAGONISTS OF SEROTONIN 5-HT6 RECEPTORS, METHODS FOR THE PRODUCTION AND THE USE THEREOF |
PE20091883A1 (es) | 2008-01-24 | 2010-01-07 | Ucb Pharma Sa | Compuestos que comprenden un grupo ciclobutoxi |
KR101709141B1 (ko) | 2008-01-25 | 2017-02-22 | 브이티브이 테라퓨틱스 엘엘씨 | TNF-α 합성의 조절자 및 PDE4 억제제로서 3고리 화합물 |
EP2252616B1 (en) | 2008-01-30 | 2014-07-23 | Genentech, Inc. | Pyrazolopyrimidine pi3k inhibitor compounds and methods of use |
JP2011511005A (ja) | 2008-02-04 | 2011-04-07 | オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド | 2−アミノピリジン系キナーゼ阻害薬 |
CN102007126A (zh) | 2008-02-22 | 2011-04-06 | Irm责任有限公司 | 作为gpr119活性调控剂的化合物和组合物 |
RU2010137300A (ru) | 2008-02-22 | 2012-03-27 | Ф. Хоффманн-Ля Рош Аг (Ch) | Модуляторы бета-амилоида |
EP2265588B1 (en) | 2008-02-27 | 2013-06-26 | Vitae Pharmaceuticals, Inc. | INHIBITORS OF 11ß -HYDROXYSTEROID DEHYDROGENASE TYPE 1 |
WO2009108827A1 (en) | 2008-02-29 | 2009-09-03 | Wyeth | Fused tricyclic pyrazolo[1, 5-a]pyrimidines, methods for preparation and uses thereof |
US8168757B2 (en) | 2008-03-12 | 2012-05-01 | Merck Sharp & Dohme Corp. | PD-1 binding proteins |
GB0804701D0 (en) | 2008-03-13 | 2008-04-16 | Amura Therapeutics Ltd | Compounds |
US8637542B2 (en) | 2008-03-14 | 2014-01-28 | Intellikine, Inc. | Kinase inhibitors and methods of use |
US8993580B2 (en) | 2008-03-14 | 2015-03-31 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
US20090246198A1 (en) | 2008-03-31 | 2009-10-01 | Takeda Pharmaceutical Company Limited | Mapk/erk kinase inhibitors and methods of use thereof |
WO2009122180A1 (en) | 2008-04-02 | 2009-10-08 | Medical Research Council | Pyrimidine derivatives capable of inhibiting one or more kinases |
US8436005B2 (en) | 2008-04-03 | 2013-05-07 | Abbott Laboratories | Macrocyclic pyrimidine derivatives |
AU2009233951B2 (en) | 2008-04-07 | 2014-02-27 | Amgen Inc. | Gem-disubstituted and spirocyclic amino pyridines/pyrimidines as cell cycle inhibitors |
WO2009124755A1 (en) | 2008-04-08 | 2009-10-15 | European Molecular Biology Laboratory (Embl) | Compounds with novel medical uses and method of identifying such compounds |
WO2009125809A1 (ja) | 2008-04-11 | 2009-10-15 | 第一三共株式会社 | ピペリジン誘導体 |
WO2009125808A1 (ja) | 2008-04-11 | 2009-10-15 | 第一三共株式会社 | アミノシクロヘキシル誘導体 |
WO2009128520A1 (ja) | 2008-04-18 | 2009-10-22 | 塩野義製薬株式会社 | P13k阻害活性を有する複素環化合物 |
WO2009131687A2 (en) | 2008-04-22 | 2009-10-29 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
US8309577B2 (en) | 2008-04-23 | 2012-11-13 | Bristol-Myers Squibb Company | Quinuclidine compounds as α-7 nicotinic acetylcholine receptor ligands |
US7863291B2 (en) | 2008-04-23 | 2011-01-04 | Bristol-Myers Squibb Company | Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands |
SG190592A1 (en) | 2008-04-29 | 2013-06-28 | Novartis Ag | Methods of monitoring the modulation of the kinase activity of fibroblast growth factor receptor and uses of said methods |
CN102015704A (zh) | 2008-04-29 | 2011-04-13 | 霍夫曼-拉罗奇有限公司 | Jnk的嘧啶基吡啶酮抑制剂 |
WO2009133127A1 (en) | 2008-04-30 | 2009-11-05 | Merck Serono S.A. | Fused bicyclic compounds and use thereof as pi3k inhibitors |
US9315449B2 (en) | 2008-05-15 | 2016-04-19 | Duke University | Substituted pyrazoles as heat shock transcription factor activators |
CN102036963B (zh) | 2008-05-23 | 2013-08-21 | 诺瓦提斯公司 | 作为蛋白酪氨酸激酶抑制剂的喹啉类和喹喔啉类衍生物 |
WO2009144205A1 (en) | 2008-05-30 | 2009-12-03 | Basf Se | Rylene-based semiconductor materials and methods of preparation and use thereof |
EP2303269B1 (en) | 2008-06-03 | 2014-07-30 | Merck Sharp & Dohme Corp. | Inhibitors of akt activity |
WO2009150150A1 (de) | 2008-06-10 | 2009-12-17 | Basf Se | Neue übergangsmetall-komplexe und deren verwendung in organischen leuchtdioden - iii |
WO2009151997A1 (en) | 2008-06-12 | 2009-12-17 | Merck & Co., Inc. | Process for producing bicycloaniline derivatives |
GB0810902D0 (en) | 2008-06-13 | 2008-07-23 | Astex Therapeutics Ltd | New compounds |
WO2009153592A1 (en) | 2008-06-19 | 2009-12-23 | Astrazeneca Ab | Pyrazole compounds 436 |
TW201004958A (en) | 2008-06-24 | 2010-02-01 | Res Found Itsuu Lab | Oxazolidinone derivatives having a fused ring |
US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
WO2010009155A2 (en) | 2008-07-14 | 2010-01-21 | Gilead Colorado, Inc. | Fused heterocyclyc inhibitor compounds |
WO2010007099A1 (en) | 2008-07-15 | 2010-01-21 | Cellzome Limited | 2-aminoimidazo[1,2-b]pyridazine derivatives as pi3k inhibitors |
CA2726460C (en) | 2008-07-15 | 2017-02-21 | F. Hoffmann-La Roche Ag | Novel phenyl-imidazopyridines and pyridazines |
UY31982A (es) | 2008-07-16 | 2010-02-26 | Boehringer Ingelheim Int | Derivados de 1,2-dihidropiridin-3-carboxamidas n-sustituidas |
EP2328897A1 (en) | 2008-07-16 | 2011-06-08 | Schering Corporation | Bicyclic heterocycle derivatives and their use as gpcr modulators |
CN102159572A (zh) | 2008-07-16 | 2011-08-17 | 先灵公司 | 双环杂环衍生物及其作为gpr 119调节剂的用途 |
WO2010009735A2 (en) | 2008-07-23 | 2010-01-28 | Dako Denmark A/S | Combinatorial analysis and repair |
JP2011530511A (ja) | 2008-08-05 | 2011-12-22 | メルク・シャープ・エンド・ドーム・コーポレイション | 治療用化合物 |
WO2010015643A1 (en) | 2008-08-06 | 2010-02-11 | Novartis Ag | New antiviral modified nucleosides |
WO2010019210A2 (en) | 2008-08-11 | 2010-02-18 | President And Fellows Of Harvard College | Halofuginone analogs for inhibition of trna synthetases and uses thereof |
UY32049A (es) | 2008-08-14 | 2010-03-26 | Takeda Pharmaceutical | Inhibidores de cmet |
US20110166135A1 (en) | 2008-09-10 | 2011-07-07 | Hiroshi Morimoto | Aromatic nitrogen-containing 6-membered ring compounds and their use |
CA2998281C (en) | 2008-09-26 | 2022-08-16 | Dana-Farber Cancer Institute, Inc. | Human anti-pd-1 antobodies and uses therefor |
US20100137313A1 (en) | 2008-10-03 | 2010-06-03 | Astrazeneca Ab | Heterocyclic derivatives and methods of use thereof |
WO2010045371A1 (en) | 2008-10-15 | 2010-04-22 | Gilead Palo Alto, Inc. | Pyrido- and pyrimido (1, 2-a) pyrimidine compounds useful as stearoyl coa desaturase inhibitors |
US8110578B2 (en) | 2008-10-27 | 2012-02-07 | Signal Pharmaceuticals, Llc | Pyrazino[2,3-b]pyrazine mTOR kinase inhibitors for oncology indications and diseases associated with the mTOR/PI3K/Akt pathway |
US20100105655A1 (en) | 2008-10-29 | 2010-04-29 | Astrazeneca Ab | Novel compounds 515 |
US8476282B2 (en) | 2008-11-03 | 2013-07-02 | Intellikine Llc | Benzoxazole kinase inhibitors and methods of use |
WO2010052448A2 (en) | 2008-11-05 | 2010-05-14 | Ucb Pharma S.A. | Fused pyrazine derivatives as kinase inhibitors |
WO2010059552A1 (en) | 2008-11-18 | 2010-05-27 | Glaxosmithkline Llc | Prolyl hydroxylase inhibitors |
US8697685B2 (en) | 2008-11-20 | 2014-04-15 | Glaxosmithkline Llc | Chemical compounds |
WO2010064621A1 (ja) | 2008-12-03 | 2010-06-10 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子材料、表示装置及び照明装置 |
KR101061599B1 (ko) | 2008-12-05 | 2011-09-02 | 한국과학기술연구원 | 비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 저해제인 신규 인다졸 유도체, 이의 약학적으로 허용가능한염 및 이를 유효성분으로 함유하는 약학적 조성물 |
WO2010077680A2 (en) | 2008-12-08 | 2010-07-08 | Vm Discovery Inc. | Compositions of protein receptor tyrosine kinase inhibitors |
US8110265B2 (en) | 2008-12-09 | 2012-02-07 | The Coca-Cola Company | Pet container and compositions having enhanced mechanical properties and gas barrier properties |
KR20180089573A (ko) | 2008-12-09 | 2018-08-08 | 제넨테크, 인크. | 항-pd-l1 항체 및 t 세포 기능을 향상시키기 위한 그의 용도 |
CA2745959A1 (en) | 2008-12-12 | 2010-06-17 | Msd K.K. | Dihydropyrimidopyrimidine derivatives |
US8507505B2 (en) | 2008-12-12 | 2013-08-13 | Msd K.K. | Dihydropyrazolopyrimidinone derivative |
SG172259A1 (en) | 2008-12-19 | 2011-07-28 | Genentech Inc | Heterocyclic compounds and methods of use |
PA8852901A1 (es) | 2008-12-22 | 2010-07-27 | Lilly Co Eli | Inhibidores de proteina cinasa |
US8263610B2 (en) | 2008-12-30 | 2012-09-11 | Arqule, Inc. | Substituted imidazolyl-5,6-dihydrobenzo[N]isoquinoline compounds |
DK2379506T3 (en) | 2008-12-30 | 2015-12-14 | Arqule Inc | Substituted 5,6-dihydro-6-phenylbenzo [f] isoquinolin-2-amine compounds |
JP5908728B2 (ja) | 2009-01-06 | 2016-04-26 | ダナ ファーバー キャンサー インスティテュート インコーポレイテッド | ピリミド−ジアゼピノンキナーゼ骨格化合物及び疾患を治療する方法 |
JOP20190231A1 (ar) | 2009-01-15 | 2017-06-16 | Incyte Corp | طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به |
EP2387315B1 (en) | 2009-01-16 | 2015-07-15 | Merck Sharp & Dohme Corp. | IMIDAZO[1,2-a]PYRIDINES AND IMIDAZO[1,2-b]PYRIDAZINES AS MARK INHIBITORS |
DE102009007038A1 (de) | 2009-02-02 | 2010-08-05 | Merck Patent Gmbh | Metallkomplexe |
JP2010180147A (ja) | 2009-02-04 | 2010-08-19 | Mitsubishi Gas Chemical Co Inc | シアン酸エステル化合物、およびその硬化物 |
JP5844159B2 (ja) | 2009-02-09 | 2016-01-13 | ユニヴェルシテ デクス−マルセイユUniversite D’Aix−Marseille | Pd−1抗体およびpd−l1抗体ならびにその使用 |
TW201038569A (en) | 2009-02-16 | 2010-11-01 | Abbott Gmbh & Co Kg | Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy |
TW201035102A (en) | 2009-03-04 | 2010-10-01 | Gruenethal Gmbh | Sulfonylated tetrahydroazolopyrazines and their use as medicinal products |
US20100278835A1 (en) | 2009-03-10 | 2010-11-04 | Astrazeneca Uk Limited | Novel compounds 660 |
WO2010104047A1 (ja) | 2009-03-11 | 2010-09-16 | 国立大学法人京都大学 | 多環芳香族化合物 |
AU2010226826A1 (en) | 2009-03-18 | 2011-10-13 | Merck Sharp & Dohme Corp. | Bicyclic compounds as inhibitors of diacylglycerol acyltransferase |
EP2411057B1 (en) | 2009-03-23 | 2020-05-06 | Eli Lilly and Company | Imaging agents for detecting neurological disorders |
WO2010111573A1 (en) | 2009-03-27 | 2010-09-30 | Abbott Laboratories | Compounds as cannabinoid receptor ligands |
WO2010117425A1 (en) | 2009-03-31 | 2010-10-14 | Biogen Idec Ma Inc. | Certain substituted pyrimidines, pharmaceutical compositions thereof, and methods for their use |
ES2465971T3 (es) | 2009-04-06 | 2014-06-09 | University Health Network | Inhibidores de quinasa y método para tratar cáncer con los mismos |
KR101675607B1 (ko) | 2009-04-07 | 2016-11-11 | 에머리티 파마 아베 | 치료제로서 이소옥사졸-3(2h)-온 유사체 |
GB0906470D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
GB0906472D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
JP5531446B2 (ja) | 2009-04-20 | 2014-06-25 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子材料、表示装置および照明装置 |
ES2347630B1 (es) | 2009-04-29 | 2011-09-08 | Universitat Ramon Llull | Sintesis y usos de 4-cianopentanoatos y 4-cianopentenoatos sustituidos. |
EP2424368B1 (en) | 2009-04-29 | 2014-12-31 | Locus Pharmaceuticals, Inc. | Pyrrolotriazine compounds |
US20100280067A1 (en) | 2009-04-30 | 2010-11-04 | Pakala Kumara Savithru Sarma | Inhibitors of acetyl-coa carboxylase |
EP2424617B1 (en) | 2009-05-01 | 2013-07-24 | Heartsine Technologies Limited | An external defibrillator |
AR078411A1 (es) | 2009-05-07 | 2011-11-09 | Lilly Co Eli | Compuesto de vinil imidazolilo y composicion farmaceutica que lo comprende |
JP5600891B2 (ja) | 2009-05-15 | 2014-10-08 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、表示装置および照明装置 |
JP5604808B2 (ja) | 2009-05-20 | 2014-10-15 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
JP5568889B2 (ja) | 2009-05-22 | 2014-08-13 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、表示装置、照明装置及び有機エレクトロルミネッセンス素子材料 |
JP5629980B2 (ja) | 2009-05-22 | 2014-11-26 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
JP5499519B2 (ja) | 2009-05-27 | 2014-05-21 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
JP2012528083A (ja) | 2009-05-27 | 2012-11-12 | コーベンハブンス ウニベルシテト | Ncamに結合する線維芽細胞増殖因子レセプター由来ペプチド |
GB0910003D0 (en) | 2009-06-11 | 2009-07-22 | Univ Leuven Kath | Novel compounds for the treatment of neurodegenerative diseases |
JP5600894B2 (ja) | 2009-06-24 | 2014-10-08 | コニカミノルタ株式会社 | 白色有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
CA2766088C (en) | 2009-06-25 | 2017-06-13 | Alkermes, Inc. | Heterocyclic compounds for the treatment of neurological and psychological disorders |
US8883888B2 (en) | 2009-06-30 | 2014-11-11 | Zeon Corporation | Diarylamine compounds, aging inhibitor, polymer composition, crosslinked rubber product and molded article of the crosslinked product, and method of producing diarylamine compound |
EP2455370A1 (en) | 2009-07-17 | 2012-05-23 | Shionogi&Co., Ltd. | Pharmaceutical product containing lactam or benzene sulfonamide compound |
US8680077B2 (en) | 2009-07-24 | 2014-03-25 | Duke University | Prochelators useful for inhibiting metal-associated toxicity |
FR2948568B1 (fr) | 2009-07-30 | 2012-08-24 | Sanofi Aventis | Formulation pharmaceutique |
TWI468402B (zh) | 2009-07-31 | 2015-01-11 | 必治妥美雅史谷比公司 | 降低β-類澱粉生成之化合物 |
IN2012DN01254A (hr) | 2009-08-05 | 2015-05-15 | Versitech Ltd | |
JP2012197231A (ja) | 2009-08-06 | 2012-10-18 | Oncotherapy Science Ltd | Ttk阻害作用を有するピリジンおよびピリミジン誘導体 |
CN102574836B (zh) | 2009-08-07 | 2014-04-16 | 中外制药株式会社 | 氨基吡唑衍生物 |
WO2011018894A1 (en) | 2009-08-10 | 2011-02-17 | Raqualia Pharma Inc. | Pyrrolopyrimidine derivatives as potassium channel modulators |
US9085560B2 (en) | 2009-08-17 | 2015-07-21 | Intellikine, Inc. | Heterocyclic compounds and uses thereof |
JP5577650B2 (ja) | 2009-08-24 | 2014-08-27 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子材料、表示装置及び照明装置 |
KR101184115B1 (ko) | 2009-08-31 | 2012-09-18 | 일동제약주식회사 | 신규 펩티드 데포르밀라제 저해제 화합물 및 그 제조방법 |
EP2473504B1 (en) | 2009-09-03 | 2015-02-25 | Bioenergenix | Heterocyclic compounds for the inhibition of pask |
US9340528B2 (en) | 2009-09-04 | 2016-05-17 | Bayer Pharma Aktiengesellschaft | Substituted aminoquinoxalines as tyrosine threonine kinase inhibitors |
WO2011031740A1 (en) | 2009-09-09 | 2011-03-17 | Achaogen, Inc. | Antibacterial fluoroquinolone analogs |
EP2475666A2 (en) | 2009-09-11 | 2012-07-18 | Trius Therapeutics, Inc. | Gyrase inhibitors |
US8426438B2 (en) | 2009-10-01 | 2013-04-23 | Merck Sharp & Dohme Corp. | Heterocyclic-fused pyrazolo[4,3-c]pyridin-3-one M1 receptor positive allosteric modulators |
US8466155B2 (en) | 2009-10-02 | 2013-06-18 | Boehringer Ingelheim International Gmbh | Pyrimidines |
GB0917571D0 (en) | 2009-10-07 | 2009-11-25 | Karobio Ab | Novel estrogen receptor ligands |
EP2308866A1 (de) | 2009-10-09 | 2011-04-13 | Bayer CropScience AG | Phenylpyri(mi)dinylpyrazole und ihre Verwendung als Fungizide |
FR2951172B1 (fr) | 2009-10-13 | 2014-09-26 | Pf Medicament | Derives pyrazolopyridines en tant qu'agent anticancereux |
CN102666537A (zh) | 2009-10-20 | 2012-09-12 | 艾格尔生物制药股份有限公司 | 治疗黄病毒科病毒感染的氮杂吲唑 |
KR20110043270A (ko) | 2009-10-21 | 2011-04-27 | (주)씨에스엘쏠라 | 유기발광화합물 및 이를 구비한 유기발광소자 |
US8507507B2 (en) | 2009-10-22 | 2013-08-13 | Gilead Sciences, Inc. | Modulators of toll-like receptors |
WO2011050245A1 (en) | 2009-10-23 | 2011-04-28 | Yangbo Feng | Bicyclic heteroaryls as kinase inhibitors |
ES2613664T3 (es) | 2009-10-26 | 2017-05-25 | Signal Pharmaceuticals, Llc | Procedimientos de síntesis y purificación de compuestos de heteroarilo |
ES2524548T3 (es) | 2009-10-30 | 2014-12-10 | Novartis Ag | N-óxido de 3-(2,6-dicloro-3,5-dimetoxi-fenil)-1-{6-[4-(4-etil-piperacin-1-il)-fenilamino]-pirimidin-4-il}-1-metil-urea |
KR20110049217A (ko) | 2009-11-04 | 2011-05-12 | 다우어드밴스드디스플레이머티리얼 유한회사 | 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자 |
GB0919432D0 (en) | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Use |
MX2012005284A (es) | 2009-11-06 | 2012-06-28 | Plexxikon Inc | Compuestos y metodos para la modulacion de cinasas. e indicaciones para ello. |
WO2011060295A1 (en) | 2009-11-13 | 2011-05-19 | Genosco | Kinase inhibitors |
KR20120097512A (ko) | 2009-11-18 | 2012-09-04 | 플렉시콘, 인코퍼레이티드 | 키나제 조절을 위한 화합물 및 방법, 및 그에 대한 적응증 |
JP2013032290A (ja) | 2009-11-20 | 2013-02-14 | Dainippon Sumitomo Pharma Co Ltd | 新規縮合ピリミジン誘導体 |
EP2504010A4 (en) | 2009-11-23 | 2013-04-17 | Merck Sharp & Dohme | Fused Bicyclic Pyrimidine Derivatives and Methods of Use Therefor |
WO2011066342A2 (en) | 2009-11-24 | 2011-06-03 | Amplimmune, Inc. | Simultaneous inhibition of pd-l1/pd-l2 |
EP2332939A1 (en) * | 2009-11-26 | 2011-06-15 | Æterna Zentaris GmbH | Novel Naphthyridine derivatives and the use thereof as kinase inhibitors |
RU2012127368A (ru) | 2009-12-01 | 2014-01-10 | Эбботт Лэборетриз | Новые трициклические соединения |
JP2011116840A (ja) | 2009-12-02 | 2011-06-16 | Fujifilm Corp | 顔料微粒子分散体、これを用いた光硬化性組成物及びカラーフィルタ |
AR079257A1 (es) | 2009-12-07 | 2012-01-04 | Novartis Ag | Formas cristalinas de 3-(2,6-dicloro-3-5-dimetoxi-fenil)-1-{6-[4-(4-etil-piperazin-1-il)-fenil-amino]-pirimidin-4-il}-1-metil-urea y sales de las mismas |
WO2011075515A1 (en) | 2009-12-17 | 2011-06-23 | Merck Sharp & Dohme Corp. | Aminopyrimidines as syk inhibitors |
EP2512476A1 (en) | 2009-12-18 | 2012-10-24 | Novartis AG | Method for treating haematological cancers |
EP2516417B1 (en) | 2009-12-22 | 2017-10-11 | Vertex Pharmaceuticals Incorporated | Isoindolinone inhibitors of phosphatidylinositol 3-kinase |
FR2954315B1 (fr) | 2009-12-23 | 2012-02-24 | Galderma Res & Dev | Nouveaux derives phenoliques, et leur utilisation pharmaceutique ou cosmetique |
WO2011079231A1 (en) | 2009-12-23 | 2011-06-30 | Gatekeeper Pharmaceutical, Inc. | Compounds that modulate egfr activity and methods for treating or preventing conditions therewith |
FR2954317B1 (fr) | 2009-12-23 | 2012-01-27 | Galderma Res & Dev | Nouveaux derives phenoliques, et leur utilisation pharmaceutique ou cosmetique |
WO2011090666A2 (en) | 2009-12-28 | 2011-07-28 | Afraxis, Inc. | Methods for treating autism |
CN102933581A (zh) | 2009-12-29 | 2013-02-13 | 破立纪元有限公司 | 作为有机半导体的硫代硫酸芳香二酰亚胺以及使用它们的器件 |
EP2519517B1 (en) | 2009-12-29 | 2015-03-25 | Dana-Farber Cancer Institute, Inc. | Type ii raf kinase inhibitors |
WO2011080755A1 (en) | 2009-12-29 | 2011-07-07 | Advinus Therapeutics Private Limited | Fused nitrogen heterocyclic compounds, process of preparation and uses thereof |
WO2011082267A2 (en) | 2009-12-30 | 2011-07-07 | Arqule, Inc. | Substituted triazolo-pyrazine compounds |
WO2011082266A2 (en) | 2009-12-30 | 2011-07-07 | Arqule, Inc. | Substituted heterocyclic compounds |
JP2013516420A (ja) | 2009-12-30 | 2013-05-13 | アークル インコーポレイテッド | 置換されたピロロ−アミノピリミジン化合物 |
CN102115026A (zh) | 2009-12-31 | 2011-07-06 | 清华大学 | 一维纳米结构、其制备方法及一维纳米结构作标记的方法 |
WO2011082400A2 (en) | 2010-01-04 | 2011-07-07 | President And Fellows Of Harvard College | Modulators of immunoinhibitory receptor pd-1, and methods of use thereof |
WO2011082488A1 (en) | 2010-01-06 | 2011-07-14 | British Columbia Cancer Agency Branch | Bisphenol derivative therapeutics and methods for their use |
KR101483215B1 (ko) | 2010-01-29 | 2015-01-16 | 한미약품 주식회사 | 단백질 키나아제 저해활성을 갖는 비시클릭 헤테로아릴 유도체 |
WO2011094890A1 (en) | 2010-02-02 | 2011-08-11 | Argusina Inc. | Phenylalanine derivatives and their use as non-peptide glp-1 receptor modulators |
WO2011097717A1 (en) | 2010-02-15 | 2011-08-18 | University Of Victoria Innovation And Development Corporation | Synthesis of bicyclic compounds and method for their use as therapeutic agents |
US9334269B2 (en) | 2010-02-17 | 2016-05-10 | Amgen Inc. | Carboxamides as inhibitors of voltage-gated sodium channels |
SA111320200B1 (ar) | 2010-02-17 | 2014-02-16 | ديبيوفارم اس ايه | مركبات ثنائية الحلقة واستخداماتها كمثبطات c-src/jak مزدوجة |
EP2536410B1 (en) | 2010-02-18 | 2015-09-23 | Merck Sharp & Dohme Corp. | Substituted pyrimidine derivatives and their use in treating viral infections |
CN102782101B (zh) | 2010-02-18 | 2015-10-07 | Ntn株式会社 | 增稠剂、润滑脂及它们的制造方法以及润滑脂封入轴承 |
US9193728B2 (en) | 2010-02-18 | 2015-11-24 | Medivation Technologies, Inc. | Fused tetracyclic pyrido [4,3-B] indole and pyrido [3,4-B] indole derivatives and methods of use |
UY33227A (es) | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de la cdk4/6 |
US9403769B2 (en) | 2010-02-22 | 2016-08-02 | Advanced Cancer Therapeutics, Llc | Small molecule inhibitors of PFKFB3 and glycolytic flux and their methods of use as anti-cancer therapeutics |
KR101719173B1 (ko) | 2010-02-26 | 2017-03-23 | 신닛테츠 수미킨 가가쿠 가부시키가이샤 | 유기 전계 발광 소자 |
WO2011109237A2 (en) | 2010-03-02 | 2011-09-09 | Emory University | Uses of noscapine and derivatives in subjects diagnosed with fap |
WO2011111880A1 (ko) | 2010-03-08 | 2011-09-15 | 주식회사 메디젠텍 | 세포핵에서 세포질로의 gsk3의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 gsk3 이동에 의해 발생되는 질환의 치료 또는 예방용 약학적 조성물 |
US20110237599A1 (en) | 2010-03-10 | 2011-09-29 | Kalypsys, Inc. | Heterocyclic inhibitors of histamine receptors for the treatment of disease |
US9562056B2 (en) | 2010-03-11 | 2017-02-07 | Gilead Connecticut, Inc. | Imidazopyridines Syk inhibitors |
US8987275B2 (en) | 2010-03-16 | 2015-03-24 | Dana-Farber Cancer Institute, Inc. | Indazole compounds and their uses |
CA2794086A1 (en) | 2010-03-24 | 2011-09-29 | Amitech Therapeutic Solutions, Inc. | Heterocyclic compounds useful for kinase inhibition |
JP5752232B2 (ja) | 2010-03-31 | 2015-07-22 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | プロテインキナーゼ阻害剤としての置換ピロロトリアジン化合物 |
CN102153551B (zh) | 2010-04-02 | 2012-04-25 | 济南海乐医药技术开发有限公司 | 基于吲唑或氮杂吲唑的双芳基脲或硫脲类结构抗肿瘤药物 |
JP5724204B2 (ja) | 2010-04-07 | 2015-05-27 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、表示装置、及び照明装置 |
US8618095B2 (en) | 2010-04-13 | 2013-12-31 | Rigel Pharmaceuticals, Inc. | 2, 4-pyrimidinediamine compounds and prodrugs thereof and their uses |
RU2012148710A (ru) | 2010-04-16 | 2014-05-27 | Новартис Аг | Органическое соединение для применения при лечении рака печени |
EP2560962B1 (en) | 2010-04-22 | 2015-05-20 | Janssen Pharmaceutica NV | Indazole compounds useful as ketohexokinase inhibitors |
AR081331A1 (es) | 2010-04-23 | 2012-08-08 | Cytokinetics Inc | Amino- pirimidinas composiciones de las mismas y metodos para el uso de los mismos |
BR112012026641A2 (pt) | 2010-04-23 | 2016-07-12 | Kineta Inc | compostos antivirais |
GB201007286D0 (en) | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
WO2011137313A1 (en) | 2010-04-30 | 2011-11-03 | Bristol-Myers Squibb Company | Aza-bicyclic amine n-oxide compounds as alpha-7 nicotinic acetylcholine receptor ligand pro-drugs |
US8759398B2 (en) | 2010-05-03 | 2014-06-24 | Biolink Life Sciences, Inc. | Phosphorus binder composition for treatment of hyperphosphatemia |
US20130137709A1 (en) | 2010-05-05 | 2013-05-30 | Nathanael S. Gray | Compounds that modulate EGFR activity and methods for treating or preventing conditions therewith |
CA2798831A1 (en) | 2010-05-11 | 2011-11-17 | Pfizer Inc. | Morpholine compounds as mineralocorticoid receptor antagonists |
RU2012153241A (ru) | 2010-05-11 | 2014-06-20 | Авео Фармасьютикалз, Инк. | Антитела к fgfr2 |
TWI513694B (zh) | 2010-05-11 | 2015-12-21 | Amgen Inc | 抑制間變性淋巴瘤激酶的嘧啶化合物 |
CA3224506A1 (en) | 2010-05-12 | 2011-11-17 | Unicycive Therapeutics, Inc. | Lanthanum carbonate hydroxide, lanthanum oxycarbonate and methods of their manufacture and use |
US8293738B2 (en) | 2010-05-12 | 2012-10-23 | Abbott Laboratories | Indazole inhibitors of kinase |
GB201008134D0 (en) | 2010-05-14 | 2010-06-30 | Medical Res Council Technology | Compounds |
WO2011147199A1 (en) | 2010-05-28 | 2011-12-01 | Versitech Limited | Compounds and methods for treating viral infections |
WO2011147198A1 (en) | 2010-05-28 | 2011-12-01 | Versitech Limited | Compounds and methods for treatment of proliferative diseases |
WO2011153553A2 (en) | 2010-06-04 | 2011-12-08 | The Regents Of The University Of California | Methods and compositions for kinase inhibition |
EP3075730B1 (en) | 2010-06-04 | 2018-10-24 | Genentech, Inc. | Aminopyrimidine derivatives as lrrk2 modulators |
WO2011155983A1 (en) | 2010-06-07 | 2011-12-15 | Bikam Pharmaceuticals Inc. | Opsin-binding ligands, compositions and methods of use |
TW201210597A (en) | 2010-06-09 | 2012-03-16 | Gilead Sciences Inc | Inhibitors of hepatitis C virus |
US8299117B2 (en) | 2010-06-16 | 2012-10-30 | Metabolex Inc. | GPR120 receptor agonists and uses thereof |
JP2013532153A (ja) | 2010-06-18 | 2013-08-15 | ザ ブリガム アンド ウィメンズ ホスピタル インコーポレイテッド | 慢性免疫病に対する免疫治療のためのtim−3およびpd−1に対する二重特異性抗体 |
US8999957B2 (en) | 2010-06-24 | 2015-04-07 | Merck Sharp & Dohme Corp. | Heterocyclic compounds as ERK inhibitors |
US8907053B2 (en) | 2010-06-25 | 2014-12-09 | Aurigene Discovery Technologies Limited | Immunosuppression modulating compounds |
WO2012005744A1 (en) | 2010-06-27 | 2012-01-12 | King Saud University | One-time password authentication with infinite nested hash claims |
ES2706066T3 (es) | 2010-07-02 | 2019-03-27 | Univ Health Network | Procedimiento dirigido a enfermedades mutantes con PTEN y composiciones para las mismas |
EP2590968A1 (en) | 2010-07-06 | 2013-05-15 | Novartis AG | Cyclic ether compounds useful as kinase inhibitors |
FR2962437B1 (fr) | 2010-07-06 | 2012-08-17 | Sanofi Aventis | Derives d'imidazopyridine, leur procede de preparation et leur application en therapeutique |
FR2962438B1 (fr) | 2010-07-06 | 2012-08-17 | Sanofi Aventis | Derives d'indolizines, procedes de preparation et application en therapeutique |
JP5810157B2 (ja) | 2010-07-09 | 2015-11-11 | ザ・ウォルター・アンド・エリザ・ホール・インスティテュート・オブ・メディカル・リサーチ | プロテインキナーゼ阻害剤および処置の方法 |
WO2012009258A2 (en) | 2010-07-13 | 2012-01-19 | Edward Roberts | Peptidomimetic galanin receptor modulators |
US20130210807A1 (en) | 2010-07-14 | 2013-08-15 | Nigel J Liverton | Tricyclic Compounds as Allosteric Modulators of Metabotropic Glutamate Receptors. |
TW201206946A (en) | 2010-07-15 | 2012-02-16 | Bristol Myers Squibb Co | Compounds for the reduction of beta-amyloid production |
KR20130091331A (ko) | 2010-07-16 | 2013-08-16 | 교와 핫꼬 기린 가부시키가이샤 | 함질소 방향족 복소환 유도체 |
WO2012008564A1 (ja) | 2010-07-16 | 2012-01-19 | 協和発酵キリン株式会社 | 含窒素芳香族複素環誘導体 |
CA2806655A1 (en) | 2010-07-28 | 2012-02-02 | Bayer Intellectual Property Gmbh | Substituted imidazo[1,2-b]pyridazines |
EP2413140A1 (en) | 2010-07-29 | 2012-02-01 | Sanofi | Method for identifying a compound having an antiarrhythmic effect as well as uses relating thereto |
JP2013539206A (ja) | 2010-07-30 | 2013-10-17 | ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド | 発光材料として電界発光化合物を使用する電界発光素子 |
WO2012019093A1 (en) | 2010-08-05 | 2012-02-09 | Human Biomolecular Research Institute | Synthetic compounds and methods to decrease nicotine self-administration |
US9051280B2 (en) | 2010-08-13 | 2015-06-09 | AbbVie Deutschland GmbH & Co. KG | Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy |
US8883839B2 (en) | 2010-08-13 | 2014-11-11 | Abbott Laboratories | Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy |
WO2012027239A1 (en) | 2010-08-23 | 2012-03-01 | Schering Corporation | NOVEL PYRAZOLO[1,5-a]PYRROLO[3,2-e]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS |
EP2608669B1 (en) | 2010-08-23 | 2016-06-22 | Merck Sharp & Dohme Corp. | NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS |
US9249123B2 (en) | 2010-09-01 | 2016-02-02 | Genentech, Inc. | Pyridinones/pyrazinones, method of making, and method of use thereof |
EP2611798B1 (en) | 2010-09-01 | 2015-04-08 | Gilead Connecticut, Inc. | Pyridazinones, method of making, and method of use thereof |
AR082799A1 (es) | 2010-09-08 | 2013-01-09 | Ucb Pharma Sa | Derivados de quinolina y quinoxalina como inhibidores de quinasa |
RS54286B1 (en) | 2010-09-08 | 2016-02-29 | Glaxosmithkline Intellectual Property Development Limited | POLYMORPHS AND SALTS N- [5- [4- (5 - {[(2R, 6S) -2,6-DIMETHYL-4-MORPHOLINYL] METHYL} -1,3-OXAZOL-2-yl) -1H-INDAZZOL- 6-IL] -2 (methyloxy) -3-pyridinyl] -methanesulfonamide |
JP5876051B2 (ja) | 2010-09-08 | 2016-03-02 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | インフルエンザウィルス感染の治療に使用するためのインダゾール誘導体 |
TWI541243B (zh) | 2010-09-10 | 2016-07-11 | 拜耳知識產權公司 | 經取代咪唑并嗒 |
WO2012035996A1 (ja) | 2010-09-14 | 2012-03-22 | 保土谷化学工業株式会社 | 電荷制御剤及びそれを用いたトナー |
CN102399233B (zh) | 2010-09-15 | 2014-08-13 | 山东轩竹医药科技有限公司 | PI3K和mTOR双重抑制剂类化合物 |
CN102399220A (zh) | 2010-09-15 | 2012-04-04 | 黄振华 | 三并环类PI3K和mTOR双重抑制剂 |
WO2012036233A1 (ja) | 2010-09-17 | 2012-03-22 | 塩野義製薬株式会社 | メラニン凝集ホルモン受容体アンタゴニスト活性を有する縮合へテロ環誘導体 |
GB201015949D0 (en) | 2010-09-22 | 2010-11-03 | Medical Res Council Technology | Compounds |
JO3062B1 (ar) | 2010-10-05 | 2017-03-15 | Lilly Co Eli | R)-(e)-2-(4-(2-(5-(1-(3، 5-داي كلورو بيريدين-4-يل)إيثوكسي)-1h-إندازول-3-يل)?ينيل)-1h-بيرازول-1-يل)إيثانول بلوري |
EP2629777B1 (en) | 2010-10-22 | 2018-12-19 | Merck Sharp & Dohme Corp. | Bicyclic diamines as janus kinase inhibitors |
PT2632467T (pt) | 2010-10-25 | 2016-08-29 | G1 Therapeutics Inc | Inibidores cdk |
JP2012092049A (ja) | 2010-10-27 | 2012-05-17 | Sumitomo Chemical Co Ltd | 有害動物防除組成物及び有害動物の防除方法 |
US9868728B2 (en) | 2010-10-29 | 2018-01-16 | Emory University | Quinazoline derivatives, compositions, and uses related thereto |
WO2012061337A1 (en) | 2010-11-02 | 2012-05-10 | Exelixis, Inc. | Fgfr2 modulators |
US20120115903A1 (en) | 2010-11-10 | 2012-05-10 | Gruenenthal Gmbh | Substituted Heteroaromatic Carboxamide and Urea Compounds as Vanilloid Receptor Ligands |
EP2638008B1 (en) | 2010-11-10 | 2015-07-01 | Actelion Pharmaceuticals Ltd | Lactam derivatives useful as orexin receptor antagonists |
JP2012116825A (ja) | 2010-11-11 | 2012-06-21 | Ehime Univ | アセンジイミド化合物の製造方法 |
KR101171232B1 (ko) | 2010-11-15 | 2012-08-06 | 단국대학교 산학협력단 | 스파이로 화합물 및 이를 포함하는 유기전계 발광소자 |
WO2012065297A1 (en) | 2010-11-16 | 2012-05-24 | Impact Therapeutics, Inc. | 3-ARYL-6-ARYL-[1,2,4]TRIAZOLO[4,3-a]PYRIDINES AS INHIBITORS OF CELL PROLIFERATION AND THE USE THEREOF |
JP2013543000A (ja) | 2010-11-17 | 2013-11-28 | アムジエン・インコーポレーテツド | 複素環化合物およびその使用 |
EP2640392B1 (en) | 2010-11-18 | 2015-01-07 | Kasina Laila Innova Pharmaceuticals Private Ltd. | Substituted 4-(selenophen-2(or 3)-ylamino)pyrimidine compounds and methods of use thereof |
GB201020179D0 (en) | 2010-11-29 | 2011-01-12 | Astex Therapeutics Ltd | New compounds |
US9090593B2 (en) | 2010-12-09 | 2015-07-28 | Amgen Inc. | Bicyclic compounds as Pim inhibitors |
JP2014503528A (ja) | 2010-12-14 | 2014-02-13 | エレクトロプホレトイクス リミテッド | カゼインキナーゼ1δ(CK1δ)阻害剤及びタウオパチーなどの神経変性疾患の治療におけるその使用 |
CN103429585B (zh) | 2010-12-20 | 2015-07-08 | 默克雪兰诺股份有限公司 | 作为白细胞介素-1受体相关激酶抑制剂的吲唑基三唑衍生物 |
AU2011348638B2 (en) | 2010-12-22 | 2015-05-21 | Leo Laboratories Limited | 3-acyl-ingenols II |
EP2468258A1 (en) | 2010-12-22 | 2012-06-27 | LEK Pharmaceuticals d.d. | Process for the preparation of a pharmaceutical composition comprising a low soluble pharmaceutically active ingredient |
US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
EP2655323B1 (en) | 2010-12-22 | 2017-12-20 | Leo Laboratories Limited | Ingenol-3-acylates iii and ingenol-3-carbamates |
MX2013007261A (es) | 2010-12-23 | 2013-11-04 | Amgen Inc | Compuestos heterociclicos y sus usos. |
JP5691508B2 (ja) | 2010-12-27 | 2015-04-01 | Jnc株式会社 | ジイミド化合物ならびにインクジェット用インクおよびその用途 |
KR101466150B1 (ko) | 2010-12-31 | 2014-11-27 | 제일모직 주식회사 | 유기광전소자용 화합물 및 이를 포함하는 유기광전소자 |
US9487726B2 (en) | 2011-01-06 | 2016-11-08 | Jx Nippon Oil & Energy Corporation | Imide compound, method for producing same, thickening agent for grease, and grease composition |
US8362023B2 (en) | 2011-01-19 | 2013-01-29 | Hoffmann-La Roche Inc. | Pyrazolo pyrimidines |
FR2970967B1 (fr) | 2011-01-27 | 2013-02-15 | Pf Medicament | Derives de type azaindazole ou diazaindazole comme medicament |
EP2487159A1 (en) | 2011-02-11 | 2012-08-15 | MSD Oss B.V. | RorgammaT inhibitors |
WO2012112961A1 (en) | 2011-02-18 | 2012-08-23 | Medivation Technologies, Inc. | Compounds and methods of treating hypertension |
JP5808826B2 (ja) | 2011-02-23 | 2015-11-10 | インテリカイン, エルエルシー | 複素環化合物およびその使用 |
TWI532742B (zh) | 2011-02-28 | 2016-05-11 | 艾伯維有限公司 | 激酶之三環抑制劑 |
RU2013146242A (ru) | 2011-03-17 | 2015-04-27 | Новартис Аг | Fgfr и его лиганды в качестве биомаркеров рака молочной железы у hr-положительных индивидуумов |
MX2013010871A (es) | 2011-03-23 | 2014-01-31 | Amgen Inc | Inhibidores dobles triciclicos fusionados de cdk 4/6 y flt3. |
ITPD20110091A1 (it) | 2011-03-24 | 2012-09-25 | Univ Padova | Inibitori multitirosinchinasi utili per le patologie correlate: modelli farmacoforici, composti identificati tramite questi modelli, metodi per la loro preparazione, la loro formulazione e il loro impiego terapeutico. |
US8802711B2 (en) | 2011-03-25 | 2014-08-12 | Abbvie Inc. | TRPV1 antagonists |
CA2828890A1 (en) | 2011-04-07 | 2012-10-11 | Genentech, Inc. | Anti-fgfr4 antibodies and methods of use |
FR2974088A1 (fr) | 2011-04-12 | 2012-10-19 | Pf Medicament | Composes pyrazolo[3,4-b]pyridines tri- et tetracycliques comme agent anticancereux |
EP2710035B1 (en) | 2011-05-16 | 2017-04-12 | F. Hoffmann-La Roche AG | Fgfr1 agonists and methods of use |
WO2012158795A1 (en) | 2011-05-17 | 2012-11-22 | Principia Biopharma Inc. | Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors |
WO2012156367A1 (en) | 2011-05-17 | 2012-11-22 | Bayer Intellectual Property Gmbh | Amino-substituted imidazopyridazines as mknk1 kinase inhibitors |
CA2834699A1 (en) | 2011-05-19 | 2012-11-22 | Novartis Ag | 4-amino-5-fluoro-3- [6- (4 -methylpiperazin- 1 - yl) - 1h - benzimidazol - 2 - yl] - 1h - quinoli n-2-one for use in the treatment of adenoid cystic carcinoma |
CA2837630A1 (en) | 2011-06-01 | 2012-12-06 | Knut Eis | Substituted aminoimidazopyridazines |
TW201316991A (zh) | 2011-06-03 | 2013-05-01 | Millennium Pharm Inc | Mek抑制劑與奧諾拉(aurora)a激酶選擇性抑制劑之組合 |
EP2719742B1 (en) | 2011-06-13 | 2016-04-27 | LG Chem, Ltd. | Novel compounds and organic electronic device using same |
ES2610366T3 (es) | 2011-06-22 | 2017-04-27 | Bayer Intellectual Property Gmbh | Heterociclil-aminoimidazopiridazinas |
US8846656B2 (en) | 2011-07-22 | 2014-09-30 | Novartis Ag | Tetrahydropyrido-pyridine and tetrahydropyrido-pyrimidine compounds and use thereof as C5a receptor modulators |
JP6123804B2 (ja) | 2011-08-12 | 2017-05-10 | 日産化学工業株式会社 | 3環性ヘテロ環化合物及びjak阻害剤 |
MX355852B (es) | 2011-08-12 | 2018-05-02 | Hoffmann La Roche | Compuestos de pirazolo [3,4-c] piridina y métodos de uso. |
JP2013049251A (ja) | 2011-08-31 | 2013-03-14 | Fujifilm Corp | レーザー彫刻用レリーフ印刷版原版、並びに、レリーフ印刷版及びその製版方法 |
WO2013033981A1 (zh) | 2011-09-06 | 2013-03-14 | 江苏先声药物研究有限公司 | 一类2,7-萘啶衍生物及其制备方法和应用 |
US9345705B2 (en) | 2011-09-15 | 2016-05-24 | Merck Sharp & Dohme Corp. | Compositions and methods for treating cancer |
EP2758400A1 (en) | 2011-09-23 | 2014-07-30 | Bayer Intellectual Property GmbH | Substituted imidazopyridazines |
US9376435B2 (en) | 2011-09-23 | 2016-06-28 | Jawaharlal Nehru Centre For Advanced Scientific Research | Chromophores for the detection of volatile organic compounds |
MX2014003889A (es) | 2011-09-30 | 2014-12-10 | Kineta Inc | Compuestos antivirales. |
UA111382C2 (uk) | 2011-10-10 | 2016-04-25 | Оріон Корпорейшн | Інгібітори протеїнкінази |
CA2850394C (en) | 2011-10-12 | 2019-05-21 | University Health Network | Indazole compounds as kinase inhibitors and method of treating cancer with same |
KR101897044B1 (ko) | 2011-10-20 | 2018-10-23 | 에스에프씨 주식회사 | 유기금속 화합물 및 이를 포함하는 유기전계발광소자 |
RU2014120792A (ru) | 2011-10-28 | 2015-12-10 | Новартис Аг | Способ лечения стромальных опухолей желудочно-кишечного тракта |
WO2013063003A1 (en) | 2011-10-28 | 2013-05-02 | Novartis Ag | Method of treating gastrointestinal stromal tumors |
WO2013088191A1 (en) | 2011-12-12 | 2013-06-20 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Antagonist of the fibroblast growth factor receptor 3 (fgfr3) for use in the treatment or the prevention of skeletal disorders linked with abnormal activation of fgfr3 |
FR2985257B1 (fr) | 2011-12-28 | 2014-02-14 | Sanofi Sa | Composes dimeres agonistes des recepteurs des fgfs (fgfrs), leur procede de preparation et leur application en therapeutique |
FR2985258A1 (fr) | 2011-12-28 | 2013-07-05 | Sanofi Sa | Composes dimeres agonistes des recepteurs des fgfs (fgfrs), leur procede de preparation et leur application en therapeutique |
WO2013109027A1 (ko) | 2012-01-18 | 2013-07-25 | 덕산하이메탈(주) | 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
US10026905B2 (en) | 2012-01-18 | 2018-07-17 | Duk San Neolux Co., Ltd. | Compound, organic electric element using the same, and an electronic device thereof |
BR112014017749B1 (pt) | 2012-01-19 | 2021-08-03 | Taiho Pharmaceutical Co., Ltd. | Composto alquinilbenzeno 3,5-dissubstituído e sal do mesmo |
CA2865021C (en) | 2012-02-23 | 2020-06-30 | Bayer Intellectual Property Gmbh | Substituted benzothienyl-pyrrolotriazines and uses thereof |
JP2013179181A (ja) | 2012-02-28 | 2013-09-09 | Sumitomo Chemical Co Ltd | 有機光電変換素子 |
CN104271577A (zh) | 2012-03-14 | 2015-01-07 | 鲁宾有限公司 | 作为mek抑制剂的杂环基化合物 |
AU2013241664B2 (en) | 2012-03-30 | 2016-05-19 | Novartis Ag | FGFR inhibitor for use in the treatment of hypophosphatemic disorders |
JP5120580B1 (ja) | 2012-05-14 | 2013-01-16 | Jsr株式会社 | 液晶配向剤 |
CN107115162B (zh) | 2012-05-20 | 2021-01-22 | 戴尔马修墨医学研究内结构和服务有限公司 | 人造二尖瓣 |
LT3495367T (lt) | 2012-06-13 | 2021-02-25 | Incyte Holdings Corporation | Pakeistieji tricikliniai junginiai, kaip fgfr inhibitoriai |
BR112015000653A2 (pt) | 2012-07-11 | 2019-11-05 | Blueprint Medicines Corp | compostos inibidores do receptor de fator de crescimento de fibroblasto, sua composição farmacêutica e seus usos |
JP2015522070A (ja) | 2012-07-11 | 2015-08-03 | ノバルティス アーゲー | 消化管間質腫瘍を治療する方法 |
CA2880901A1 (en) | 2012-08-02 | 2014-02-06 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
WO2014019186A1 (en) | 2012-08-02 | 2014-02-06 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
KR101985259B1 (ko) | 2012-08-10 | 2019-06-03 | 제이에스알 가부시끼가이샤 | 액정 배향제 및 화합물 |
WO2014044846A1 (en) | 2012-09-24 | 2014-03-27 | Evotec (Uk) Ltd. | 3-(aryl- or heteroaryl-amino)-7-(3,5-dimethoxyphenyl)isoquinoline derivatives as fgfr inhibitors useful for the treatment of proliferative disorders or dysplasia |
WO2014048878A1 (en) | 2012-09-26 | 2014-04-03 | Evotec (Uk) Ltd. | Phenyl- or pyridyl- pyrrolo[2,3b]pyrazine derivatives useful in the treatment or prevention of proliferative disorders or dysplasia |
WO2014062454A1 (en) | 2012-10-15 | 2014-04-24 | Merck Sharp & Dohme Corp. | Compositions and methods for treating cancer |
KR102000211B1 (ko) | 2012-10-29 | 2019-09-30 | 삼성디스플레이 주식회사 | 유기금속 화합물 및 이를 포함한 유기 발광 소자 |
US20140148548A1 (en) | 2012-11-28 | 2014-05-29 | Central Glass Company, Limited | Fluorine-Containing Polymerizable Monomer And Polymer Compound Using Same |
RU2660349C2 (ru) | 2012-11-28 | 2018-07-05 | Мерк Шарп И Доум Корп. | Композиции и способы для лечения злокачественной опухоли |
CN104968664A (zh) | 2012-12-12 | 2015-10-07 | 山东亨利医药科技有限责任公司 | 作为酪氨酸激酶抑制剂的并环化合物 |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
WO2014105849A1 (en) | 2012-12-28 | 2014-07-03 | Xoma (Us) Llc | Antibodies specific for fgfr4 and methods of use |
TWI629266B (zh) | 2012-12-28 | 2018-07-11 | 藍印藥品公司 | 纖維母細胞生長因子受體之抑制劑 |
KR102030587B1 (ko) | 2013-01-09 | 2019-10-10 | 에스에프씨주식회사 | 두 개의 나프틸기를 포함하는 비대칭 안트라센 유도체 및 이를 포함하는 유기 발광 소자 |
CN103694236B (zh) | 2013-01-15 | 2017-05-31 | 苏州开拓药业股份有限公司 | 一种嘧啶骨架具有刺猬通路拮抗剂活性的抗肿瘤化合物 |
WO2014113191A1 (en) | 2013-01-15 | 2014-07-24 | Xiaohu Zhang | Hedgehog pathway signaling inhibitors and therapeutic applications thereof |
KR101456626B1 (ko) | 2013-02-01 | 2014-11-03 | 대영이앤비 주식회사 | 냉장고 부압 방지 장치 |
WO2014136972A1 (ja) | 2013-03-07 | 2014-09-12 | 国立大学法人九州大学 | 超分子複合体、発光体、および有機化合物検出用のセンサー素子 |
WO2014138485A1 (en) | 2013-03-08 | 2014-09-12 | Irm Llc | Ex vivo production of platelets from hematopoietic stem cells and the product thereof |
EP2968285A4 (en) | 2013-03-13 | 2016-12-21 | Flatley Discovery Lab | COMPOUNDS AND METHODS FOR THE TREATMENT OF CYSTIC FIBROSIS |
US9498532B2 (en) | 2013-03-13 | 2016-11-22 | Novartis Ag | Antibody drug conjugates |
US9163019B2 (en) | 2013-03-14 | 2015-10-20 | AbbVie Deutschland GmbH & Co. KG | Inhibitor compounds of phosphodiesterase type 10A |
MY181020A (en) | 2013-03-15 | 2020-12-16 | Sanofi Sa | Heteroaryl compounds and uses thereof |
TWI647220B (zh) | 2013-03-15 | 2019-01-11 | 美商西建卡爾有限責任公司 | 雜芳基化合物及其用途 |
WO2014160521A1 (en) | 2013-03-15 | 2014-10-02 | Blueprint Medicines Corporation | Piperazine derivatives and their use as kit modulators |
TWI628176B (zh) | 2013-04-04 | 2018-07-01 | 奧利安公司 | 蛋白質激酶抑制劑 |
KR101573611B1 (ko) | 2013-04-17 | 2015-12-01 | 주식회사 엘지화학 | 플러렌 유도체, 이를 이용한 유기 태양 전지 및 이의 제조 방법 |
SI2986610T1 (en) | 2013-04-19 | 2018-04-30 | Incyte Holdings Corporation | Bicyclic heterocycles as inhibitors of FGFR |
EP2986630B1 (en) | 2013-04-19 | 2018-08-15 | Covagen AG | Novel bispecific binding molecules with antitumoral activity |
GB201307577D0 (en) | 2013-04-26 | 2013-06-12 | Astex Therapeutics Ltd | New compounds |
CA2911706A1 (en) | 2013-05-09 | 2014-11-13 | Principia Biopharma Inc. | Quinolone derivatives as fibroblast growth factor inhibitors |
KR20160021134A (ko) | 2013-06-14 | 2016-02-24 | 사노피 | 방광암 치료용 피라졸로피리딘 유도체 |
CN109369671B (zh) | 2013-06-28 | 2021-07-27 | 百济神州有限公司 | 作为Raf激酶和/或Raf激酶二聚体抑制剂的稠合三环脲类化合物 |
US9670231B2 (en) | 2013-06-28 | 2017-06-06 | Beigene, Ltd. | Fused tricyclic amide compounds as multiple kinase inhibitors |
ES2807599T3 (es) | 2013-07-02 | 2021-02-23 | Syngenta Participations Ag | Heterociclos bi- o tricíclicos activos como plaguicidas con sustituyentes que contienen azufre |
EP3019491A4 (en) | 2013-07-09 | 2016-12-21 | Dana Farber Cancer Inst Inc | KINASE INHIBITORS FOR THE TREATMENT OF DISEASE |
JP6018547B2 (ja) | 2013-07-09 | 2016-11-02 | 大成ロテック株式会社 | 舗装機械 |
WO2015006754A2 (en) | 2013-07-11 | 2015-01-15 | Acea Biosciences Inc. | Heterocyclic compounds and uses thereof |
TW201605452A (zh) | 2013-08-28 | 2016-02-16 | 安斯泰來製藥股份有限公司 | 以嘧啶化合物作爲有效成分之醫藥組成物 |
SG11201602069WA (en) | 2013-10-18 | 2016-04-28 | Eisai R&D Man Co Ltd | Pyrimidine fgfr4 inhibitors |
EP3060560A1 (en) | 2013-10-25 | 2016-08-31 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
US9266883B2 (en) | 2013-10-25 | 2016-02-23 | Novartis Ag | Ring-fused bicyclic pyridyl derivatives as FGFR4 inhibitors |
FR3012330B1 (fr) | 2013-10-29 | 2015-10-23 | Oreal | Composition biphase comprenant un ester d'acide gras et de sucre ou un alkylpolyglucoside liquide, de hlb < 8, et un alcane ramifie en c8-c18 |
WO2015066452A2 (en) | 2013-11-01 | 2015-05-07 | Foundation Medicine, Inc. | Methods of treating pediatric cancers |
US9695165B2 (en) | 2014-01-15 | 2017-07-04 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
MA38393B1 (fr) | 2014-03-13 | 2018-11-30 | Sanofi Sa | Composés hétéroaryle et utilisations associées |
BR112017003312B1 (pt) | 2014-08-19 | 2023-05-02 | Shanghai Haihe Pharmaceutical Co., Ltd. | Compostos de indazol como inibidores de fgfr quinase, preparação e uso dos mesmos |
CN104262330B (zh) | 2014-08-27 | 2016-09-14 | 广东东阳光药业有限公司 | 一种脲取代联苯类化合物及其组合物及用途 |
US10350206B2 (en) | 2014-09-19 | 2019-07-16 | Bayer Pharma Aktiengesellschaft | Benzyl substituted indazoles as BUB1 inhibitors |
WO2016064960A1 (en) | 2014-10-22 | 2016-04-28 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
EP3259246B1 (en) | 2015-02-20 | 2023-03-22 | Oregon Health & Science University | Derivatives of sobetirome |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
SG10201913036RA (en) | 2015-02-20 | 2020-02-27 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
KR20240039186A (ko) | 2015-06-03 | 2024-03-26 | 트리아스텍 인코포레이티드 | 제형 및 이의 용도 |
DK3322701T3 (da) | 2015-07-15 | 2019-07-08 | H Hoffmann La Roche Ag | Ethynylderivater som metabotropiske glutamatreceptormodulatorer |
GB2556571B (en) | 2015-07-15 | 2021-07-07 | Cabot Corp | Methods of making an elastomer composite reinforced with silica and products containing same |
SG10201912066SA (en) | 2015-07-15 | 2020-02-27 | Protagonist Therapeutics Inc | Peptide inhibitors of interleukin-23 receptor and their use to treat inflammatory diseases |
GB201512369D0 (en) | 2015-07-15 | 2015-08-19 | Immatics Biotechnologies Gmbh | Novel peptides and combination of peptides for use in immunotherapy against epithelial ovarian cancer and other cancers |
CN107847574B (zh) | 2015-07-30 | 2023-05-23 | 宏观基因有限公司 | Pd-1结合分子和其使用方法 |
WO2017023972A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc. | 3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof |
US10188634B2 (en) | 2015-08-03 | 2019-01-29 | Samumed, Llc | 3-(3H-imidazo[4,5-C]pyridin-2-yl)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof |
WO2017024004A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc. | 3-(1h-pyrrolo[2,3-b]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof |
WO2017024015A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc. | 3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof |
WO2017023989A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc. | 3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof |
US10231956B2 (en) | 2015-08-03 | 2019-03-19 | Samumed, Llc | 3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof |
US10519169B2 (en) | 2015-08-03 | 2019-12-31 | Samumed, Llc | 3-(1H-pyrrolo[2,3-C]pyridin-2-yl)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof |
US10696687B2 (en) | 2015-08-20 | 2020-06-30 | Changzhou Jiekai Pharmatech Co., Ltd. | Pyrazolo fused heterocyclic compounds as ERK inhibitors |
EP3356349A1 (en) | 2015-09-28 | 2018-08-08 | Araxes Pharma LLC | Inhibitors of kras g12c mutant proteins |
US20170107216A1 (en) | 2015-10-19 | 2017-04-20 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
EP3365335B1 (en) | 2015-10-23 | 2024-02-14 | Array Biopharma, Inc. | 2-aryl- and 2-heteroaryl-substituted 2-pyridazin-3(2h)-one compounds as inhibitors of fgfr tyrosine kinases |
SG10202004618TA (en) | 2015-11-19 | 2020-06-29 | Incyte Corp | Heterocyclic compounds as immunomodulators |
US20170174671A1 (en) | 2015-12-17 | 2017-06-22 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
MD3394033T2 (ro) | 2015-12-22 | 2021-04-30 | Incyte Corp | Compuși heterociclici ca imunomodulatori |
US20170320875A1 (en) | 2016-05-06 | 2017-11-09 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
WO2017205464A1 (en) | 2016-05-26 | 2017-11-30 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
BR112018076534A2 (pt) | 2016-06-20 | 2019-04-02 | Incyte Corporation | compostos heterocíclicos como imunomoduladores |
AR108875A1 (es) | 2016-06-24 | 2018-10-03 | Incyte Corp | COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE PI3K-g |
ES2930092T3 (es) | 2016-07-14 | 2022-12-07 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
EP3504198B1 (en) | 2016-08-29 | 2023-01-25 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
WO2018041091A1 (en) | 2016-08-30 | 2018-03-08 | Sunshine Lake Pharma Co., Ltd. | Inhibitors of influenza virus replication, application methods and uses thereof |
WO2018049214A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyridine derivatives as hpk1 modulators and uses thereof for the treatment of cancer |
JP6949952B2 (ja) | 2016-10-05 | 2021-10-13 | リキュリウム アイピー ホールディングス リミテッド ライアビリティー カンパニー | スピロ環化合物 |
KR101755556B1 (ko) | 2016-11-18 | 2017-07-07 | 주식회사 케마스 | 육산화사비소의 결정다형을 포함하는 뇌암 예방 또는 치료용 약학 조성물 및 이의 제조방법 |
KR101834366B1 (ko) | 2016-11-21 | 2018-03-05 | 주식회사 케마스 | 육산화사비소의 결정다형을 포함하는 유방암 예방 또는 치료용 약학 조성물 및 이의 제조방법 |
KR101844049B1 (ko) | 2016-12-05 | 2018-03-30 | 주식회사 케마스 | 육산화사비소의 결정다형을 포함하는 간암 예방 또는 치료용 약학 조성물 |
KR101844050B1 (ko) | 2016-12-09 | 2018-05-14 | 주식회사 케마스 | 육산화사비소의 결정다형을 포함하는 암 예방 또는 치료용 약학 조성물 |
MA47120A (fr) | 2016-12-22 | 2021-04-28 | Incyte Corp | Dérivés pyridine utilisés en tant qu'immunomodulateurs |
WO2018119263A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Heterocyclic compounds derivatives as pd-l1 internalization inducers |
UA126394C2 (uk) | 2016-12-22 | 2022-09-28 | Інсайт Корпорейшн | Похідні бензоксазолу як імуномодулятори |
WO2018119236A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Triazolo[1,5-a]pyridine derivatives as immunomodulators |
TWI798192B (zh) | 2016-12-22 | 2023-04-11 | 美商英塞特公司 | 免疫調節劑化合物及使用方法 |
EP3558963B1 (en) | 2016-12-22 | 2022-03-23 | Incyte Corporation | Bicyclic heteroaromatic compounds as immunomodulators |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
WO2018234354A1 (en) | 2017-06-20 | 2018-12-27 | Grünenthal GmbH | NOVEL SUBSTITUTED 3-INDOLE AND 3-INDAZOLE COMPOUNDS AS PHOSPHODIESTERASE INHIBITORS |
CN111032656B (zh) | 2017-08-22 | 2022-12-02 | 捷思英达医药技术(上海)有限公司 | 杂环化合物激酶抑制剂及其药物组合物和应用 |
CA3079607A1 (en) | 2017-10-19 | 2019-04-25 | Effector Therapeutics, Inc. | Benzimidazole-indole inhibitors of mnk1 and mnk2 |
HUE057581T2 (hu) | 2017-12-02 | 2022-05-28 | Galapagos Nv | Új vegyületek és ezeket tartalmazó gyógyszerkészítmények betegségek kezelésére |
CN112135824B (zh) | 2018-03-30 | 2024-11-05 | 因赛特公司 | 作为免疫调节剂的杂环化合物 |
EP3788046A1 (en) | 2018-05-04 | 2021-03-10 | Incyte Corporation | Salts of an fgfr inhibitor |
WO2019213544A2 (en) | 2018-05-04 | 2019-11-07 | Incyte Corporation | Solid forms of an fgfr inhibitor and processes for preparing the same |
MD3790877T2 (ro) | 2018-05-11 | 2023-08-31 | Incyte Corp | Derivați de tetrahidro-imidazo[4,5-c]piridină în calitate de imunomodulatori PD-L1 |
EP3836923B1 (en) | 2018-08-14 | 2024-10-16 | OssiFi Therapeutics LLC | Pyrrolo - dipyridine compounds for the treatment of bone loss |
ES2954572T3 (es) | 2018-09-07 | 2023-11-23 | Merck Patent Gmbh | Derivados de 5-morfolin-4-il-pirazolo[4,3-b]piridina |
US20220041579A1 (en) | 2018-12-19 | 2022-02-10 | Array Biopharma Inc. | Substituted quinoxaline compounds as inhibitors of fgfr tyrosine kinases |
JP2022515198A (ja) | 2018-12-19 | 2022-02-17 | アレイ バイオファーマ インコーポレイテッド | FGFRチロシンキナーゼの阻害剤としての置換ピラゾロ[1,5-a]ピリジン化合物 |
JP7148802B2 (ja) | 2019-01-25 | 2022-10-06 | 富士通株式会社 | 解析プログラム、解析方法および解析装置 |
US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
US12122767B2 (en) | 2019-10-01 | 2024-10-22 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
JP2022552324A (ja) | 2019-10-14 | 2022-12-15 | インサイト・コーポレイション | Fgfr阻害剤としての二環式複素環 |
WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
CN115151539A (zh) | 2019-12-04 | 2022-10-04 | 因赛特公司 | Fgfr抑制剂的衍生物 |
US11897891B2 (en) | 2019-12-04 | 2024-02-13 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
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