DOP2016000299A - Derivados de pirrolidina-2,5-diona, composiciones farmacéuticas y su uso como inhibidores ido1 - Google Patents
Derivados de pirrolidina-2,5-diona, composiciones farmacéuticas y su uso como inhibidores ido1Info
- Publication number
- DOP2016000299A DOP2016000299A DO2016000299A DO2016000299A DOP2016000299A DO P2016000299 A DOP2016000299 A DO P2016000299A DO 2016000299 A DO2016000299 A DO 2016000299A DO 2016000299 A DO2016000299 A DO 2016000299A DO P2016000299 A DOP2016000299 A DO P2016000299A
- Authority
- DO
- Dominican Republic
- Prior art keywords
- pirrolidine
- pharmaceutical compositions
- ido1 inhibitors
- formula
- relates
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
- C07D207/404—2,5-Pyrrolidine-diones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. succinimide
- C07D207/408—Radicals containing only hydrogen and carbon atoms attached to ring carbon atoms
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4015—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil having oxo groups directly attached to the heterocyclic ring, e.g. piracetam, ethosuximide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/46—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Reproductive Health (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Steroid Compounds (AREA)
Abstract
La presente invención se refiere al compuesto de la fórmula I o sus enantiómeros, sales, solvatos o profármacos farmacéuticamente aceptables. La invención también se refiere al uso de los compuestos de la fórmula I como inhibidores de IDO1. La invención también se refiere al uso de los compuestos de la fórmula I para el tratamiento y/o la prevención de cáncer y endometriosis. La invención también se refiere a un proceso para preparar los compuestos de la fórmula I.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201461996976P | 2014-05-15 | 2014-05-15 | |
EP14168534 | 2014-05-15 | ||
BE2014/0754A BE1021251B1 (fr) | 2014-05-15 | 2014-10-21 | Derives de pyrrolidine-2,5-dione, compositions pharmaceutiques et methodes d'utilisation comme inhibiteurs de ido1 |
Publications (1)
Publication Number | Publication Date |
---|---|
DOP2016000299A true DOP2016000299A (es) | 2017-03-15 |
Family
ID=54479389
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DO2016000299A DOP2016000299A (es) | 2014-05-15 | 2016-11-15 | Derivados de pirrolidina-2,5-diona, composiciones farmacéuticas y su uso como inhibidores ido1 |
Country Status (20)
Country | Link |
---|---|
US (3) | US9603836B2 (es) |
EP (1) | EP3148531A1 (es) |
JP (1) | JP6231226B2 (es) |
KR (1) | KR101873672B1 (es) |
CN (1) | CN106536480B (es) |
AP (1) | AP2016009527A0 (es) |
AU (1) | AU2015260826B2 (es) |
CA (1) | CA2948842C (es) |
CU (1) | CU20160162A7 (es) |
DO (1) | DOP2016000299A (es) |
EA (1) | EA201650031A1 (es) |
IL (1) | IL248915A0 (es) |
MD (1) | MD20160118A2 (es) |
MX (1) | MX2016015005A (es) |
PE (1) | PE20170247A1 (es) |
SG (1) | SG11201608708WA (es) |
TN (1) | TN2016000501A1 (es) |
TW (1) | TWI567059B (es) |
UY (1) | UY36122A (es) |
WO (1) | WO2015173764A1 (es) |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB201311891D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel compound |
GB201311888D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
CN106536480B (zh) | 2014-05-15 | 2019-09-03 | 艾特奥斯治疗公司 | 吡咯烷-2,5-二酮衍生物、药物组合物及用作ido1抑制剂的方法 |
CA2979616C (en) | 2015-03-17 | 2020-04-28 | Pfizer Inc. | Novel 3-indol substituted derivatives, pharmaceutical compositions and methods for use |
CA2929850A1 (en) * | 2015-05-14 | 2016-11-14 | Pfizer Inc. | Combination therapies comprising a pyrrolidine-2,5-dione ido1 inhibitor |
ES2889906T3 (es) | 2015-05-21 | 2022-01-14 | Harpoon Therapeutics Inc | Proteínas de unión triespecíficas y usos médicos |
WO2017025868A1 (en) | 2015-08-10 | 2017-02-16 | Pfizer Inc. | 3-indol substituted derivatives, pharmaceutical compositions and methods for use |
MX2018008797A (es) | 2016-01-19 | 2018-11-29 | Pfizer | Vacunas contra el cancer. |
JP2019507773A (ja) * | 2016-03-09 | 2019-03-22 | ネザーランズ トランスレーショナル リサーチ センター ビー.ブイ. | インドールアミン2,3−ジオキシゲナーゼの阻害剤 |
CN109790143A (zh) | 2016-05-10 | 2019-05-21 | C4医药公司 | 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体 |
CN109641874A (zh) | 2016-05-10 | 2019-04-16 | C4医药公司 | 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体 |
CN109562107A (zh) | 2016-05-10 | 2019-04-02 | C4医药公司 | 用于靶蛋白降解的杂环降解决定子体 |
US11623958B2 (en) | 2016-05-20 | 2023-04-11 | Harpoon Therapeutics, Inc. | Single chain variable fragment CD3 binding proteins |
CN109952300B (zh) | 2016-09-24 | 2022-01-18 | 百济神州有限公司 | 5或8-取代的咪唑并[1,5-a]吡啶 |
WO2018089301A1 (en) * | 2016-11-08 | 2018-05-17 | The Johns Hopkins University | Pharmaceutical treatments for preventing or treating pancreatic cancer |
EP3570832A4 (en) | 2017-01-17 | 2020-06-10 | Board Of Regents, The University Of Texas System | NOVEL COMPOUNDS USEFUL AS INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE AND / OR TRYPTOPHANE DIOXYGENASE |
WO2018209298A1 (en) | 2017-05-12 | 2018-11-15 | Harpoon Therapeutics, Inc. | Mesothelin binding proteins |
AU2018277559A1 (en) | 2017-05-30 | 2019-10-17 | Bristol-Myers Squibb Company | Compositions comprising a combination of an anti-LAG-3 antibody, a PD-1 pathway inhibitor, and an immunotherapeutic agent |
SG11202000197PA (en) | 2017-07-11 | 2020-02-27 | Pfizer | Immunogenic compositions comprising cea muc1 and tert |
CN110997682A (zh) | 2017-08-17 | 2020-04-10 | 爱杜西亚药品有限公司 | 吲哚胺2,3-二氧酶及/或色氨酸2,3-二氧酶的抑制剂 |
EP3676263B1 (en) | 2017-09-01 | 2021-10-06 | Netherlands Translational Research Center B.V. | 3-hydroxy-imidazolidin-4-one compounds as inhibitors of indoleamine 2,3-dioxygenase |
KR20220111743A (ko) | 2017-10-13 | 2022-08-09 | 하푼 테라퓨틱스, 인크. | B 세포 성숙화 항원 결합 단백질 |
CA3087807A1 (en) | 2018-01-15 | 2019-07-18 | Idorsia Pharmaceuticals Ltd | Inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan 2,3-dioxygenase |
WO2020018670A1 (en) | 2018-07-17 | 2020-01-23 | Board Of Regents, The University Of Texas System | Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase |
BE1026615B1 (fr) | 2018-09-27 | 2020-07-06 | Iteos Therapeutics S A | Combinaison d’un inhibiteur du récepteur a2a et d'un agent anticancéreux |
AU2019337974A1 (en) | 2018-09-11 | 2021-04-08 | iTeos Belgium SA | Thiocarbamate derivatives as A2A inhibitors, pharmaceutical composition thereof and combinations with anticancer agents |
US11376255B2 (en) | 2018-09-11 | 2022-07-05 | iTeos Belgium SA | Thiocarbamate derivatives as A2A inhibitors, pharmaceutical composition thereof and combinations with anticancer agents |
EP3856771A4 (en) | 2018-09-25 | 2022-06-29 | Harpoon Therapeutics, Inc. | Dll3 binding proteins and methods of use |
US20220259212A1 (en) | 2019-07-11 | 2022-08-18 | Idorsia Pharmaceuticals Ltd | Inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan 2,3-dioxygenase |
WO2021024020A1 (en) | 2019-08-06 | 2021-02-11 | Astellas Pharma Inc. | Combination therapy involving antibodies against claudin 18.2 and immune checkpoint inhibitors for treatment of cancer |
AR122421A1 (es) | 2020-04-16 | 2022-09-07 | iTeos Belgium SA | Métodos y formulaciones para la administración de inhibidores a2a derivados de tiocarbamato |
AU2021306613A1 (en) | 2020-07-07 | 2023-02-02 | BioNTech SE | Therapeutic RNA for HPV-positive cancer |
TW202245808A (zh) | 2020-12-21 | 2022-12-01 | 德商拜恩迪克公司 | 用於治療癌症之治療性rna |
WO2022135667A1 (en) | 2020-12-21 | 2022-06-30 | BioNTech SE | Therapeutic rna for treating cancer |
WO2022135666A1 (en) | 2020-12-21 | 2022-06-30 | BioNTech SE | Treatment schedule for cytokine proteins |
EP4294948A1 (en) | 2021-02-17 | 2023-12-27 | iTeos Belgium SA | Compounds, compositions and methods of treatment thereof |
EP4052705A1 (en) | 2021-03-05 | 2022-09-07 | Universität Basel Vizerektorat Forschung | Compositions for the treatment of ebv associated diseases or conditions |
BR112023017582A2 (pt) | 2021-03-05 | 2023-12-05 | Univ Basel | Composições para o tratamento de doenças ou condições associadas ao ebv |
CA3225254A1 (en) | 2021-07-13 | 2023-01-19 | BioNTech SE | Multispecific binding agents against cd40 and cd137 in combination therapy for cancer |
TW202333802A (zh) | 2021-10-11 | 2023-09-01 | 德商拜恩迪克公司 | 用於肺癌之治療性rna(二) |
AU2023230110A1 (en) | 2022-03-08 | 2024-10-24 | Alentis Therapeutics Ag | Use of anti-claudin-1 antibodies to increase t cell availability |
WO2024126457A1 (en) | 2022-12-14 | 2024-06-20 | Astellas Pharma Europe Bv | Combination therapy involving bispecific binding agents binding to cldn18.2 and cd3 and immune checkpoint inhibitors |
Family Cites Families (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE509731C2 (sv) | 1996-05-14 | 1999-03-01 | Labwell Ab | Metod för palladium-katalyserade organiska reaktioner innefattande ett uppvärmningssteg utfört med mikrovågsenergi |
JP2000095759A (ja) | 1998-07-21 | 2000-04-04 | Takeda Chem Ind Ltd | 三環性化合物、その製造法および剤 |
US6265403B1 (en) | 1999-01-20 | 2001-07-24 | Merck & Co., Inc. | Angiogenesis inhibitors |
MXPA04002070A (es) | 2001-09-19 | 2004-06-07 | Pharmacia Corp | Compuestos de indazol sustituidos para el tratamiento de la inflamacion. |
IL164082A0 (en) | 2002-03-28 | 2005-12-18 | Eisai Co Ltd | Azaindole derivatives and pharmaceutical compositions containing the same |
TW200307542A (en) | 2002-05-30 | 2003-12-16 | Astrazeneca Ab | Novel compounds |
FR2845996A1 (fr) | 2002-10-16 | 2004-04-23 | Servier Lab | Nouveaux derives de[3,4-a:3,4-c]carbazole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
CN101265254A (zh) | 2003-03-27 | 2008-09-17 | 兰肯瑙医学研究所 | 新型ido抑制剂及其使用方法 |
FR2862647B1 (fr) | 2003-11-25 | 2008-07-04 | Aventis Pharma Sa | Derives de pyrazolyle, procede de preparation et intermediaires de ce procede a titre de medicaments et de compositions pharmaceutiques les renfermant |
GB0328909D0 (en) | 2003-12-12 | 2004-01-14 | Syngenta Participations Ag | Chemical compounds |
GB0415746D0 (en) | 2004-07-14 | 2004-08-18 | Novartis Ag | Organic compounds |
NZ560225A (en) * | 2005-02-09 | 2010-10-29 | Arqule Inc | Maleimide derivatives, pharmaceutical compositions and methods for treatment of cancer |
WO2007039580A1 (en) | 2005-10-05 | 2007-04-12 | Nycomed Gmbh | Imidazolyl-substituted benzophenone compounds |
WO2007045622A1 (en) | 2005-10-18 | 2007-04-26 | Nycomed Gmbh | Oxazolo [4 , 5-b] pyridine compounds as nitric oxide synthase inhibitors |
WO2007050963A1 (en) | 2005-10-27 | 2007-05-03 | Lankenau Institute For Medical Research | Novel ido inhibitors and methods of use thereof |
WO2007087488A2 (en) | 2006-01-24 | 2007-08-02 | Eli Lilly And Company | Indole sulfonamide modulators of progesterone receptors |
JP5255559B2 (ja) | 2006-03-31 | 2013-08-07 | アボット・ラボラトリーズ | インダゾール化合物 |
AU2007240548A1 (en) | 2006-04-05 | 2007-11-01 | Novartis Ag | Combinations of therapeutic agents for treating cancer |
GB0624308D0 (en) | 2006-12-05 | 2007-01-17 | Molmed Spa | Combination product |
CN101595093A (zh) | 2006-12-07 | 2009-12-02 | 诺瓦提斯公司 | 有机化合物 |
JP2010518014A (ja) | 2007-01-31 | 2010-05-27 | バーテックス ファーマシューティカルズ インコーポレイテッド | キナーゼ阻害剤として有用な2−アミノピリジン誘導体 |
US8389568B2 (en) | 2007-03-16 | 2013-03-05 | Lankenau Institute For Medical Research | IDO inhibitors and methods of use thereof |
CA2694224A1 (en) | 2007-07-25 | 2009-01-29 | Boehringer Ingelheim International Gmbh | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
US7868001B2 (en) | 2007-11-02 | 2011-01-11 | Hutchison Medipharma Enterprises Limited | Cytokine inhibitors |
AU2008331480A1 (en) | 2007-11-30 | 2009-06-11 | Glaxosmithkline Llc | Prolyl hydroxylase inhibitors |
WO2009118292A1 (en) | 2008-03-24 | 2009-10-01 | Novartis Ag | Arylsulfonamide-based matrix metalloprotease inhibitors |
US20110159017A1 (en) | 2008-04-11 | 2011-06-30 | Ludwig Institute For Cancer Research Ltd. | Trytophan catabolism in cancer treatment and diagnosis |
DE102008052943A1 (de) | 2008-10-23 | 2010-04-29 | Merck Patent Gmbh | Azaindolderivate |
BRPI0922565A2 (pt) | 2008-12-19 | 2015-12-15 | Bristol Myers Squibb Co | compostos de carbazol carboxamida úteis como inibidores de cinase |
JP2012518011A (ja) | 2009-02-17 | 2012-08-09 | バーテックス ファーマシューティカルズ インコーポレイテッド | ホスファチジルイノシトール3−キナーゼのテトラヒドロチアゾロピリジン阻害剤 |
SG182247A1 (en) | 2009-05-27 | 2012-08-30 | Hoffmann La Roche | Bicyclic indole-pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
KR101256018B1 (ko) | 2009-08-20 | 2013-04-18 | 한국과학기술연구원 | 단백질 키나아제 저해활성을 갖는 1,3,6-치환된 인돌 화합물 |
WO2011038163A1 (en) * | 2009-09-23 | 2011-03-31 | Medivation Technologies, Inc. | Pyrido[3,4-b]indoles and methods of use |
IN2012DN02679A (es) | 2009-10-12 | 2015-09-04 | Bayer Cropscience Ag | |
CA2777565C (en) | 2009-10-13 | 2019-06-18 | Ligand Pharmaceuticals Inc. | Hematopoietic growth factor mimetic diphenylamine small molecule compounds and their uses |
WO2012068406A2 (en) | 2010-11-18 | 2012-05-24 | Ligand Pharmaceuticals Incorporated | Use of hematopoietic growth factor mimetics |
AU2012230890A1 (en) | 2011-03-22 | 2013-09-26 | Amgen Inc. | Azole compounds as Pim inhibitors |
EP2714677B1 (en) | 2011-05-23 | 2018-08-22 | Merck Patent GmbH | Pyridine-and pyrazine derivatives |
CA2844799A1 (en) | 2011-08-17 | 2013-02-21 | Amgen Inc. | Heteroaryl sodium channel inhibitors |
US20160263087A1 (en) | 2013-11-08 | 2016-09-15 | Iteos Therapeutics | Novel 4-(indol-3-yl)-pyrazole derivatives, pharmaceutical compositions and methods for use |
US9126984B2 (en) | 2013-11-08 | 2015-09-08 | Iteos Therapeutics | 4-(indol-3-yl)-pyrazole derivatives, pharmaceutical compositions and methods for use |
WO2015121812A1 (en) | 2014-02-12 | 2015-08-20 | Iteos Therapeutics | Novel 3-(indol-3-yl)-pyridine derivatives, pharmaceutical compositions and methods for use |
WO2015140717A1 (en) | 2014-03-18 | 2015-09-24 | Iteos Therapeutics | Novel 3-indol substituted derivatives, pharmaceutical compositions and methods for use |
US20150266857A1 (en) | 2014-03-18 | 2015-09-24 | Iteos Therapeutics | Novel 3-indol substituted derivatives, pharmaceutical compositions and methods for use |
CN106536480B (zh) | 2014-05-15 | 2019-09-03 | 艾特奥斯治疗公司 | 吡咯烷-2,5-二酮衍生物、药物组合物及用作ido1抑制剂的方法 |
-
2015
- 2015-05-14 CN CN201580024882.8A patent/CN106536480B/zh not_active Expired - Fee Related
- 2015-05-14 TW TW104115441A patent/TWI567059B/zh not_active IP Right Cessation
- 2015-05-14 PE PE2016002241A patent/PE20170247A1/es not_active Application Discontinuation
- 2015-05-14 EA EA201650031A patent/EA201650031A1/ru unknown
- 2015-05-14 US US14/711,911 patent/US9603836B2/en active Active
- 2015-05-14 WO PCT/IB2015/053557 patent/WO2015173764A1/en active Application Filing
- 2015-05-14 CA CA2948842A patent/CA2948842C/en active Active
- 2015-05-14 TN TN2016000501A patent/TN2016000501A1/en unknown
- 2015-05-14 MD MDA20160118A patent/MD20160118A2/ro not_active Application Discontinuation
- 2015-05-14 KR KR1020167031517A patent/KR101873672B1/ko active IP Right Grant
- 2015-05-14 SG SG11201608708WA patent/SG11201608708WA/en unknown
- 2015-05-14 MX MX2016015005A patent/MX2016015005A/es unknown
- 2015-05-14 UY UY0001036122A patent/UY36122A/es not_active Application Discontinuation
- 2015-05-14 AU AU2015260826A patent/AU2015260826B2/en not_active Ceased
- 2015-05-14 EP EP15731680.3A patent/EP3148531A1/en not_active Withdrawn
- 2015-05-14 JP JP2016567533A patent/JP6231226B2/ja not_active Expired - Fee Related
-
2016
- 2016-05-14 AP AP2016009527A patent/AP2016009527A0/en unknown
- 2016-10-21 US US15/331,446 patent/US9949951B2/en active Active
- 2016-11-08 CU CUP2016000162A patent/CU20160162A7/es unknown
- 2016-11-13 IL IL248915A patent/IL248915A0/en unknown
- 2016-11-15 DO DO2016000299A patent/DOP2016000299A/es unknown
-
2018
- 2018-03-23 US US15/934,246 patent/US10398679B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
KR101873672B1 (ko) | 2018-07-02 |
EP3148531A1 (en) | 2017-04-05 |
WO2015173764A1 (en) | 2015-11-19 |
US9603836B2 (en) | 2017-03-28 |
US20150329525A1 (en) | 2015-11-19 |
UY36122A (es) | 2016-01-08 |
IL248915A0 (en) | 2017-01-31 |
CN106536480B (zh) | 2019-09-03 |
JP6231226B2 (ja) | 2017-11-15 |
TW201605794A (zh) | 2016-02-16 |
US9949951B2 (en) | 2018-04-24 |
EA201650031A1 (ru) | 2017-06-30 |
US10398679B2 (en) | 2019-09-03 |
CN106536480A8 (zh) | 2017-06-30 |
CA2948842A1 (en) | 2015-11-19 |
AU2015260826B2 (en) | 2019-10-24 |
US20180214415A1 (en) | 2018-08-02 |
SG11201608708WA (en) | 2016-11-29 |
TN2016000501A1 (en) | 2018-04-04 |
CA2948842C (en) | 2019-09-24 |
AU2015260826A1 (en) | 2016-11-03 |
JP2017515850A (ja) | 2017-06-15 |
CU20160162A7 (es) | 2017-03-03 |
KR20160146807A (ko) | 2016-12-21 |
US20170035731A1 (en) | 2017-02-09 |
AP2016009527A0 (en) | 2016-10-31 |
MD20160118A2 (ro) | 2017-04-30 |
MX2016015005A (es) | 2017-09-28 |
PE20170247A1 (es) | 2017-03-29 |
CN106536480A (zh) | 2017-03-22 |
TWI567059B (zh) | 2017-01-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DOP2016000299A (es) | Derivados de pirrolidina-2,5-diona, composiciones farmacéuticas y su uso como inhibidores ido1 | |
DOP2015000158A (es) | Inhibidores de prmt5 y sus usos | |
DOP2017000151A (es) | Derivados de quinazolina utilizados para tratar el vih | |
CO2018000589A2 (es) | Oxiesteroles y composiciones farmacéuticas que los contienen | |
CU20160188A7 (es) | Compuestos de indazole substituidos como inhibidores de irak4 | |
UY37900A (es) | Nuevos derivados de rapamicina | |
CO2017006962A2 (es) | Derivados de 2-anilinopirimidina sustituida como moudladores de egfr | |
CL2016001790A1 (es) | Compuestos derivados y composiciones de n-azaspirocicloalcano n-heteroaril sustituido para inhibir la actividad de shp2. | |
CO2017000362A2 (es) | Compuestos de derivados heterocíclicos sustituidos como inhibidores de demtilasa-1 específica lisina | |
CU24517B1 (es) | Derivados de carbonucleósidos sustituidos útiles como agentes antineoplásicos | |
UY36244A (es) | Derivados de la pirimidinona como inhibidores del factor xia y/o de la calicreína plasmática y composiciones farmacéuticas que los contienen | |
DOP2015000270A (es) | Potenciador de inhibidores del homólogo de zeste | |
UY35617A (es) | Inhibidores de la fosfatidilinositol 3-quinasa | |
UY35951A (es) | HETEROARILOS y USOS DE ESTOS | |
EA201992183A2 (ru) | Синтез полициклических карбамоилпиридоновых соединений | |
NZ726608A (en) | Phosphatidylinositol 3-kinase inhibitors | |
NZ726360A (en) | Phosphatidylinositol 3-kinase inhibitors | |
NZ726638A (en) | Phosphatidylinositol 3-kinase inhibitors | |
DOP2018000062A (es) | Piridinona dicaboxamidas para uso como inhibidores de bromodominio | |
MX2018001992A (es) | Compuestos triciclicos heterociclicos como inhibidores de fosfoinositol 3-quinasa. | |
CR20170496A (es) | Nuevos compuestos y derivados de sulfonimidoilpurinona para el tratamiento y profilaxis de infecciones víricas | |
CL2018003121A1 (es) | Inhibidores del potenciador del homólogo zeste 2. | |
CO2017000011A2 (es) | Derivados de quinolizinona como inhibidores de pi3k | |
UY36758A (es) | Inhibidores del potenciador del homólogo zeste 2 | |
TR201819805T4 (tr) | Flavaglin türevleri̇. |