JP5229853B2 - 癌その他の疾患の治療に有用な新規な二環尿素誘導体 - Google Patents
癌その他の疾患の治療に有用な新規な二環尿素誘導体 Download PDFInfo
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- JP5229853B2 JP5229853B2 JP2006508978A JP2006508978A JP5229853B2 JP 5229853 B2 JP5229853 B2 JP 5229853B2 JP 2006508978 A JP2006508978 A JP 2006508978A JP 2006508978 A JP2006508978 A JP 2006508978A JP 5229853 B2 JP5229853 B2 JP 5229853B2
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- amino
- carbonyl
- carboxamide
- phenoxy
- methyl
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 64
- 125000004076 pyridyl group Chemical group 0.000 claims description 51
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- 150000003839 salts Chemical class 0.000 claims description 26
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- 125000001624 naphthyl group Chemical group 0.000 claims description 22
- 229910052736 halogen Inorganic materials 0.000 claims description 20
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 17
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 13
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- 125000003118 aryl group Chemical group 0.000 claims description 9
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- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 claims description 7
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 7
- 125000004429 atom Chemical group 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
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- 125000000355 1,3-benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 3
- MDWCRJBTKOKVQG-UHFFFAOYSA-N 1-[4-(2-acetylpyridin-4-yl)oxyphenyl]-3-(1-methylindazol-5-yl)urea Chemical compound C1=NC(C(=O)C)=CC(OC=2C=CC(NC(=O)NC=3C=C4C=NN(C)C4=CC=3)=CC=2)=C1 MDWCRJBTKOKVQG-UHFFFAOYSA-N 0.000 claims description 3
- BBZKKWAPVWOMAJ-UHFFFAOYSA-N 4-[4-(1,3-benzothiazol-6-ylcarbamoylamino)phenoxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=CC(NC(=O)NC=3C=C4SC=NC4=CC=3)=CC=2)=C1 BBZKKWAPVWOMAJ-UHFFFAOYSA-N 0.000 claims description 3
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- DLHNNZXUBYYDHZ-UHFFFAOYSA-N n-cyclopropyl-4-[4-[(1-methylindazol-5-yl)carbamoylamino]phenoxy]pyridine-2-carboxamide Chemical compound C=1C=C2N(C)N=CC2=CC=1NC(=O)NC(C=C1)=CC=C1OC(C=1)=CC=NC=1C(=O)NC1CC1 DLHNNZXUBYYDHZ-UHFFFAOYSA-N 0.000 claims description 3
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- 125000005955 1H-indazolyl group Chemical group 0.000 claims description 2
- BEYKSLQDBANGNU-UHFFFAOYSA-N 4-[3-(1h-indazol-5-ylcarbamoylamino)phenoxy]-n-methylpyridine-2-carboxamide;dihydrochloride Chemical compound Cl.Cl.C1=NC(C(=O)NC)=CC(OC=2C=C(NC(=O)NC=3C=C4C=NNC4=CC=3)C=CC=2)=C1 BEYKSLQDBANGNU-UHFFFAOYSA-N 0.000 claims description 2
- HAZFKZCXSBGRBZ-UHFFFAOYSA-N 4-[3-[(1-methylindazol-5-yl)carbamoylamino]phenoxy]-n-(2-piperidin-1-ylethyl)pyridine-2-carboxamide Chemical compound C=1C=C2N(C)N=CC2=CC=1NC(=O)NC(C=1)=CC=CC=1OC(C=1)=CC=NC=1C(=O)NCCN1CCCCC1 HAZFKZCXSBGRBZ-UHFFFAOYSA-N 0.000 claims description 2
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- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 2
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- CUTKPPQPQQZTNJ-UHFFFAOYSA-N n-methyl-4-[3-[(1-methylindazol-5-yl)carbamoylamino]phenoxy]pyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C(NC(=O)NC=3C=C4C=NN(C)C4=CC=3)C=CC=2)=C1 CUTKPPQPQQZTNJ-UHFFFAOYSA-N 0.000 claims description 2
- AMWGHPUETVUZKW-UHFFFAOYSA-N 4-[3-chloro-4-(2,3-dihydro-1h-inden-5-ylcarbamoylamino)phenoxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C(Cl)C(NC(=O)NC=3C=C4CCCC4=CC=3)=CC=2)=C1 AMWGHPUETVUZKW-UHFFFAOYSA-N 0.000 claims 3
- YBVJTMVJQXXCMZ-UHFFFAOYSA-N 4-[4-[(5-chloro-1,3-benzoxazol-2-yl)carbamoylamino]phenoxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=CC(NC(=O)NC=3OC4=CC=C(Cl)C=C4N=3)=CC=2)=C1 YBVJTMVJQXXCMZ-UHFFFAOYSA-N 0.000 claims 2
- IZUCKVLYRXFQLH-UHFFFAOYSA-N 4-[4-[(6-chloro-1,3-benzothiazol-2-yl)carbamoylamino]-3-fluorophenoxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C(F)C(NC(=O)NC=3SC4=CC(Cl)=CC=C4N=3)=CC=2)=C1 IZUCKVLYRXFQLH-UHFFFAOYSA-N 0.000 claims 2
- HBAUQPPKUSRWAE-UHFFFAOYSA-N 4-[4-[(6-methoxy-1,3-benzothiazol-2-yl)carbamoylamino]phenoxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=CC(NC(=O)NC=3SC4=CC(OC)=CC=C4N=3)=CC=2)=C1 HBAUQPPKUSRWAE-UHFFFAOYSA-N 0.000 claims 2
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- GQCCVDYTEWSNLE-UHFFFAOYSA-N 4-[2,4-dichloro-5-[(1-methylindazol-5-yl)carbamoylamino]phenoxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C(=CC(Cl)=C(NC(=O)NC=3C=C4C=NN(C)C4=CC=3)C=2)Cl)=C1 GQCCVDYTEWSNLE-UHFFFAOYSA-N 0.000 claims 1
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- HHJUWIANJFBDHT-KOTLKJBCSA-N vindesine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(N)=O)N4C)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 HHJUWIANJFBDHT-KOTLKJBCSA-N 0.000 description 1
- 229960004355 vindesine Drugs 0.000 description 1
- GBABOYUKABKIAF-GHYRFKGUSA-N vinorelbine Chemical compound C1N(CC=2C3=CC=CC=C3NC=22)CC(CC)=C[C@H]1C[C@]2(C(=O)OC)C1=CC([C@]23[C@H]([C@]([C@H](OC(C)=O)[C@]4(CC)C=CCN([C@H]34)CC2)(O)C(=O)OC)N2C)=C2C=C1OC GBABOYUKABKIAF-GHYRFKGUSA-N 0.000 description 1
- 229960002066 vinorelbine Drugs 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000008215 water for injection Substances 0.000 description 1
- 230000037314 wound repair Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 235000016804 zinc Nutrition 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US45034803P | 2003-02-28 | 2003-02-28 | |
US60/450,348 | 2003-02-28 | ||
PCT/US2004/006287 WO2004078748A2 (en) | 2003-02-28 | 2004-03-01 | Novel bicyclic urea derivatives useful in the treatment of cancer and other disorders |
Publications (2)
Publication Number | Publication Date |
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JP2006519265A JP2006519265A (ja) | 2006-08-24 |
JP5229853B2 true JP5229853B2 (ja) | 2013-07-03 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2006508978A Expired - Lifetime JP5229853B2 (ja) | 2003-02-28 | 2004-03-01 | 癌その他の疾患の治療に有用な新規な二環尿素誘導体 |
Country Status (5)
Country | Link |
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EP (1) | EP1608639A2 (es) |
JP (1) | JP5229853B2 (es) |
CA (1) | CA2516931C (es) |
MX (1) | MXPA05009104A (es) |
WO (1) | WO2004078748A2 (es) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002534468A (ja) | 1999-01-13 | 2002-10-15 | バイエル コーポレイション | p38キナーゼ阻害剤としてのω−カルボキシアリール置換ジフェニル尿素 |
US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
EP1580188B9 (en) | 2002-02-11 | 2012-05-23 | Bayer HealthCare, LLC | Aryl ureas as kinase inhibitors |
DK1478358T3 (da) | 2002-02-11 | 2013-10-07 | Bayer Healthcare Llc | Sorafenibtosylat til behandling af sygdomme kendetegnet ved unormal angiogenese |
EP1626714B1 (en) | 2003-05-20 | 2007-07-04 | Bayer Pharmaceuticals Corporation | Diaryl ureas for diseases mediated by pdgfr |
BRPI0412219B8 (pt) | 2003-07-23 | 2021-07-27 | Bayer Healthcare Llc | compostos ômega-carboxi aril difenil uréia fluoro substituídos e composições farmacêuticas compreendendo os referidos compostos |
US7071182B2 (en) * | 2003-12-23 | 2006-07-04 | Abbott Laboratories | Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor |
CA2557398A1 (en) * | 2004-02-26 | 2005-09-09 | Hans-Peter Buchstaller | Benzimidazolyl derivatives as kinase inhibitors |
EP1799661A1 (en) * | 2004-10-08 | 2007-06-27 | AstraZeneca AB | New hydroxymethylbenzothiazoles amides |
DE602006017188D1 (de) | 2005-03-07 | 2010-11-11 | Bayer Schering Pharma Ag | Pharmazeutische zusammensetzung mit einem omega-carboxyaryl-substituierten diphenylharnstoff zur behandlung von krebs |
BRPI0502016B8 (pt) * | 2005-06-03 | 2021-05-25 | Univ Federal Do Rio De Janeiro Ufrj | composto ureídicos, composições farmacêuticas contendo os mesmos e seu uso no tratamento de doenças inflamatórias |
EA015198B1 (ru) * | 2006-03-23 | 2011-06-30 | Биота Юроп Лимитед | Антибактериальные агенты |
DE102006029795A1 (de) * | 2006-06-27 | 2008-01-03 | Schebo Biotech Ag | Neue Harnstoff-Derivate und deren Verwendungen |
EP2134677B1 (en) | 2006-12-20 | 2011-10-12 | Bayer HealthCare LLC | 4-{4-[({3-tert-butyl-1-[3-(hydroxymethyl)phenyl]-1h-pyrazol-5-yl}carbamoyl)-amino]-3-chlorophenoxy}-n-methylpyridine-2-carboxamide as an inhibitor of the vegfr kinase for the treatment of cancer |
AR067927A1 (es) | 2007-08-15 | 2009-10-28 | Glaxo Group Ltd | Quinolinas sustituidas, composiciones y combinaciones que las comprenden y el uso de las mismas en la preparacion de un medicamento para tratamiento de enfermedades inflamatorias y/o alergicas del tracto respiratorio. |
CN102295600A (zh) * | 2011-09-08 | 2011-12-28 | 天津大学 | 5-氨基-8-羟基喹啉的制备方法 |
WO2013138753A1 (en) | 2012-03-16 | 2013-09-19 | Fox Chase Chemical Diversity Center, Inc. | Prodrugs of riluzole and their method of use |
CN103508961B (zh) | 2012-06-26 | 2015-07-22 | 中美冠科生物技术(太仓)有限公司 | 抗肿瘤药物 |
CN104250226B (zh) * | 2013-06-27 | 2019-04-26 | 常州方楠医药技术有限公司 | 一种制备瑞格菲尼中间体的方法 |
WO2017047803A1 (ja) * | 2015-09-17 | 2017-03-23 | 三栄源エフ・エフ・アイ株式会社 | 増粘多糖類含有製剤の製造方法 |
US10519113B2 (en) * | 2016-08-17 | 2019-12-31 | Icahn School Of Medicine At Mount Sinai | Kinase inhibitor compounds, compositions, and methods of treating cancer |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6001930A (en) | 1997-03-13 | 1999-12-14 | Acushnet Company | Golf ball forming compositions comprising polyamide blended with sulfonated or phosphonated polymers |
KR20010031912A (ko) * | 1997-11-10 | 2001-04-16 | 스티븐 비. 데이비스 | 벤조티아졸 단백질 티로신 키나제 억제제 |
AU762077B2 (en) | 1997-12-22 | 2003-06-19 | Bayer Healthcare Llc | Inhibition of p38 kinase activity using aryl and heteroaryl substituted heterocyclic ureas |
IL136773A0 (en) | 1997-12-22 | 2001-06-14 | Bayer Ag | Inhibition of raf kinase aryl and heteroaryl substituted heterocyclic ureas |
BR9814374B1 (pt) * | 1997-12-22 | 2013-09-17 | "urÉias heterocÍclicas substituÍdas e composiÇÕes compreendendo as mesmas" | |
JP3887769B2 (ja) | 1997-12-22 | 2007-02-28 | バイエル コーポレイション | 対称および非対称ジフェニル尿素を用いるp38キナーゼの阻害 |
IL136690A0 (en) | 1997-12-22 | 2001-06-14 | Bayer Ag | Inhibition of raf kinase using symmetrical and unsymmetrical substituted diphenyl ureas |
MXPA00006233A (es) | 1997-12-22 | 2002-09-18 | Bayer Ag | Inhibicion de la actividad de la cinasa p38 utilizando ureas heterociclicas sustituidas. |
US7928239B2 (en) * | 1999-01-13 | 2011-04-19 | Bayer Healthcare Llc | Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas |
RU2319693C9 (ru) * | 1999-01-13 | 2008-08-20 | Байер Копэрейшн | Производные мочевины (варианты), фармацевтическая композиция (варианты) и способ лечения заболевания, связанного с ростом раковых клеток (варианты) |
WO2000042012A1 (en) * | 1999-01-13 | 2000-07-20 | Bayer Corporation | φ-CARBOXYARYL SUBSTITUTED DIPHENYL UREAS AS RAF KINASE INHIBITORS |
JP2002534468A (ja) | 1999-01-13 | 2002-10-15 | バイエル コーポレイション | p38キナーゼ阻害剤としてのω−カルボキシアリール置換ジフェニル尿素 |
US20020065296A1 (en) * | 1999-01-13 | 2002-05-30 | Bayer Corporation | Heteroaryl ureas containing nitrogen hetero-atoms as p38 kinase inhibitors |
AU1617901A (en) * | 1999-11-16 | 2001-05-30 | Boehringer Ingelheim Pharmaceuticals, Inc. | Urea derivatives as anti-inflammatory agents |
ES2323876T3 (es) | 2001-04-18 | 2009-07-27 | Euro-Celtique S.A. | Derivados de 1-(4-piperidinil)-1,3-dihidro-2h-benzoxazol-2-ona y compuestos relacionados como analogos de la nociceptina y ligandos de orl1 para el tratamiento del dolor. |
WO2002085857A2 (en) * | 2001-04-20 | 2002-10-31 | Bayer Corporation | Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas |
DK1478358T3 (da) * | 2002-02-11 | 2013-10-07 | Bayer Healthcare Llc | Sorafenibtosylat til behandling af sygdomme kendetegnet ved unormal angiogenese |
WO2004078128A2 (en) * | 2003-02-28 | 2004-09-16 | Bayer Pharmaceuticals Corporation | Substituted pyridine derivatives useful in the treatment of cancer and other disorders |
-
2004
- 2004-03-01 MX MXPA05009104A patent/MXPA05009104A/es unknown
- 2004-03-01 EP EP04716166A patent/EP1608639A2/en not_active Withdrawn
- 2004-03-01 JP JP2006508978A patent/JP5229853B2/ja not_active Expired - Lifetime
- 2004-03-01 CA CA2516931A patent/CA2516931C/en not_active Expired - Fee Related
- 2004-03-01 WO PCT/US2004/006287 patent/WO2004078748A2/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
EP1608639A2 (en) | 2005-12-28 |
JP2006519265A (ja) | 2006-08-24 |
CA2516931A1 (en) | 2004-09-16 |
WO2004078748A2 (en) | 2004-09-16 |
CA2516931C (en) | 2014-09-09 |
MXPA05009104A (es) | 2006-05-31 |
WO2004078748A3 (en) | 2004-11-11 |
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