ZA987491B - Naphthyridinones for inhibiting protein tyrosine kinase and cell cycle kinase mediated cellular proliferation - Google Patents
Naphthyridinones for inhibiting protein tyrosine kinase and cell cycle kinase mediated cellular proliferationInfo
- Publication number
- ZA987491B ZA987491B ZA987491A ZA987491A ZA987491B ZA 987491 B ZA987491 B ZA 987491B ZA 987491 A ZA987491 A ZA 987491A ZA 987491 A ZA987491 A ZA 987491A ZA 987491 B ZA987491 B ZA 987491B
- Authority
- ZA
- South Africa
- Prior art keywords
- cell cycle
- cellular proliferation
- naphthyridinones
- protein tyrosine
- kinase
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US5674697P | 1997-08-20 | 1997-08-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA987491B true ZA987491B (en) | 1999-04-21 |
Family
ID=22006345
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA987491A ZA987491B (en) | 1997-08-20 | 1998-08-19 | Naphthyridinones for inhibiting protein tyrosine kinase and cell cycle kinase mediated cellular proliferation |
Country Status (13)
Country | Link |
---|---|
US (1) | US6150359A (xx) |
EP (1) | EP1003745B1 (xx) |
JP (1) | JP4965021B2 (xx) |
KR (1) | KR20010023089A (xx) |
AT (1) | ATE286053T1 (xx) |
AU (1) | AU742999B2 (xx) |
BR (1) | BR9811956B1 (xx) |
CA (1) | CA2291222C (xx) |
DE (1) | DE69828408T2 (xx) |
ES (1) | ES2235353T3 (xx) |
NZ (1) | NZ502704A (xx) |
WO (1) | WO1999009030A1 (xx) |
ZA (1) | ZA987491B (xx) |
Families Citing this family (55)
Publication number | Priority date | Publication date | Assignee | Title |
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EP1801112A1 (en) * | 1998-05-26 | 2007-06-27 | Warner-Lambert Company LLC | Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation |
DE69939168D1 (de) * | 1998-05-26 | 2008-09-04 | Warner Lambert Co | Bicyclische pyrimidine und bicyclische 3,4-dihydropyrimidine als inhibitoren der zellvermehrung |
US7005434B2 (en) | 2001-01-19 | 2006-02-28 | Sb Corporation | Compounds and uses thereof |
US6756374B2 (en) | 2001-01-22 | 2004-06-29 | Hoffmann-La Roche Inc. | Diaminothiazoles having antiproliferative activity |
NZ527741A (en) | 2001-02-26 | 2005-02-25 | Tanabe Seiyaku Co | Pyridopyrimidine or naphthyridine derivative |
US6822097B1 (en) * | 2002-02-07 | 2004-11-23 | Amgen, Inc. | Compounds and methods of uses |
US20040005567A1 (en) * | 2002-07-02 | 2004-01-08 | Isis Pharmaceuticals Inc. | Antisense modulation of cyclin-dependent kinase 4 expression |
RU2376029C2 (ru) | 2002-04-25 | 2009-12-20 | Юниверсити Оф Коннектикут Хелт Сентер | Применение белков теплового шока для улучшения терапевтического эффекта невакцинного лечебного воздействия |
PA8577501A1 (es) * | 2002-07-25 | 2004-02-07 | Warner Lambert Co | Inhibidores de quinasas |
JP4252534B2 (ja) * | 2002-08-06 | 2009-04-08 | エフ.ホフマン−ラ ロシュ アーゲー | p−38MAPキナーゼインヒビターとしての6−アルコキシ−ピリド−ピリミジン類 |
US20040147561A1 (en) * | 2002-12-27 | 2004-07-29 | Wenge Zhong | Pyrid-2-one derivatives and methods of use |
BRPI0406809A (pt) * | 2003-01-17 | 2005-12-27 | Warner Lambert Co | Heterociclos substituìdos de 2-aminopiridina como inibidores da proliferação celular |
EP1673343A4 (en) * | 2003-10-08 | 2008-09-10 | Irm Llc | COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS |
EP1699477A2 (en) * | 2003-12-11 | 2006-09-13 | Theravance, Inc. | Compositions for use in the treatment of mutant receptor tyrosine kinase driven cellular proliferative diseases |
US7211576B2 (en) | 2004-04-20 | 2007-05-01 | Hoffmann-La Roche Inc. | Diaminothiazoles |
TW200800983A (en) | 2005-09-14 | 2008-01-01 | Janssen Pharmaceutica Nv | 5-oxo-5,8-dihydro-pyrido-pyrimidines as inhibitors of C-FMS kinase |
US7642270B2 (en) | 2005-09-14 | 2010-01-05 | Janssen Pharmaceutica N.V. | 5-oxo-5,8-dihydro-pyrido-pyrimidine as inhibitors of c-fms kinase |
KR20080045279A (ko) * | 2005-09-14 | 2008-05-22 | 얀센 파마슈티카 엔.브이. | C-fms 키나제 저해제로서의5-옥소-5,8-디하이드로-피리도-피리미딘 |
JP2010509265A (ja) * | 2006-11-09 | 2010-03-25 | エフ.ホフマン−ラ ロシュ アーゲー | キナーゼ阻害剤としての置換6−フェニル−ピリド[2,3−d]ピリミジン−7−オン誘導体及びそれの使用方法 |
US20100173426A1 (en) * | 2006-12-19 | 2010-07-08 | Johnson Faye M | Biomaker identifying the reactivation of stat3 after src inhibition |
WO2008104473A2 (en) * | 2007-02-28 | 2008-09-04 | F. Hoffmann-La Roche Ag | Pyrazolopyriidine derivatives and their use as kinase inhibitors |
CL2009000400A1 (es) | 2008-02-22 | 2010-09-10 | Irm Llc | Compuestos heterociclicos derivados de 3-fenil-1,6- naftiridin-2-ona; moduladores de la actividad cinasa; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como trastornos alergicos, trastornos autoinmunes, neoplasias, rechazo en trasplante de organos, entre otras. |
CN101684119B (zh) * | 2008-09-27 | 2012-11-28 | 中国科学院上海药物研究所 | 5,8-二取代-1,6-二氮杂萘-7-羰酰胺类化合物及其制备方法、组合物和用途 |
EP4438734A2 (en) | 2010-06-14 | 2024-10-02 | The Scripps Research Institute | Reprogramming of cells to a new fate |
US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
ES2704744T3 (es) | 2012-06-13 | 2019-03-19 | Incyte Holdings Corp | Compuestos tricíclicos sustituidos como inhibidores de FGFR |
WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
CN104812756A (zh) * | 2012-09-26 | 2015-07-29 | 曼凯德公司 | 多激酶通路抑制剂 |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
CN109776525B (zh) | 2013-04-19 | 2022-01-21 | 因赛特控股公司 | 作为fgfr抑制剂的双环杂环 |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
AU2016219822B2 (en) | 2015-02-20 | 2020-07-09 | Incyte Holdings Corporation | Bicyclic heterocycles as FGFR inhibitors |
US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
WO2018108167A1 (zh) * | 2016-12-16 | 2018-06-21 | 基石药业 | Cdk4/6抑制剂 |
CN108264511B (zh) * | 2017-01-03 | 2021-04-13 | 浙江海正药业股份有限公司 | 杂环类衍生物及其制备方法和其在医药上的用途 |
US11174255B2 (en) | 2017-05-15 | 2021-11-16 | University Of Houston System | Pyrido[2,3-d]pyrimidin-7-ones and related compounds as inhibitors of protein kinases |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
BR112020022392A2 (pt) | 2018-05-04 | 2021-02-02 | Incyte Corporation | formas sólidas de um inibidor de fgfr e processos para preparação das mesmas |
MX2020011639A (es) | 2018-05-04 | 2021-02-15 | Incyte Corp | Sales de un inhibidor de receptores de factor de crecimiento de fibroblastos (fgfr). |
AU2019384646A1 (en) * | 2018-11-20 | 2021-06-17 | Nflection Therapeutics, Inc. | Naphthyridinone-aniline compounds for treatment of dermal disorders |
WO2020140055A1 (en) * | 2018-12-28 | 2020-07-02 | Spv Therapeutics Inc. | Cyclin-dependent kinase inhibitors |
WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
CA3137869A1 (en) | 2019-05-16 | 2020-11-19 | Gregory Cuny | Protein kinase inhibitors and uses thereof for the treatment of diseases and conditions |
US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
JP2022550539A (ja) * | 2019-10-01 | 2022-12-02 | ゴールドフィンチ バイオ,インク. | Cdk5の置換1,6-ナフチリジン阻害剤 |
IL291901A (en) | 2019-10-14 | 2022-06-01 | Incyte Corp | Bicyclyl heterocycles as fgr suppressors |
WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
WO2021113479A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
KR20220131900A (ko) | 2019-12-04 | 2022-09-29 | 인사이트 코포레이션 | Fgfr 억제제의 유도체 |
WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
AR122928A1 (es) * | 2020-07-10 | 2022-10-19 | Goldfinch Bio Inc | 1,6-naftiridinas sustituidas inhibidoras de cdk5 |
CA3215903A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
US20240287062A1 (en) * | 2021-05-07 | 2024-08-29 | Enliven Inc. | Naphthyridone compounds for inhibition of raf kinases and/or bcr-abl tyrosine kinases |
EP4352059A1 (en) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1171218A (en) * | 1967-11-09 | 1969-11-19 | Parke Davis & Co | New Heterocyclic Amine Compounds and Methods for their Production |
US3639401A (en) * | 1969-07-28 | 1972-02-01 | Parke Davis & Co | 6-aryl-2 7-bis((trialkylsilyl)amino)pyrido (2 3-d)pyrimidine compounds |
US4271164A (en) * | 1979-04-16 | 1981-06-02 | Warner-Lambert Company | 6-Substituted-arylpyrido[2,3-d]pyrimidin-7-amines and derivatives |
US5409930A (en) * | 1991-05-10 | 1995-04-25 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
FR2706898B1 (xx) * | 1993-06-25 | 1995-09-08 | Union Pharma Scient Appl | |
MX9702245A (es) * | 1994-11-14 | 1997-06-28 | Warner Lambert Co | Seis-aril-pirido(2,3-d)pirimidinas y naftiridinas para inhibir la proliferacion celular mediada por la proteina cinasa tirosina. |
US5620981A (en) * | 1995-05-03 | 1997-04-15 | Warner-Lambert Company | Pyrido [2,3-D]pyrimidines for inhibiting protein tyrosine kinase mediated cellular proliferation |
-
1998
- 1998-08-13 WO PCT/US1998/016848 patent/WO1999009030A1/en not_active Application Discontinuation
- 1998-08-13 US US09/463,553 patent/US6150359A/en not_active Expired - Lifetime
- 1998-08-13 AT AT98939941T patent/ATE286053T1/de not_active IP Right Cessation
- 1998-08-13 CA CA002291222A patent/CA2291222C/en not_active Expired - Fee Related
- 1998-08-13 JP JP2000509710A patent/JP4965021B2/ja not_active Expired - Fee Related
- 1998-08-13 BR BRPI9811956-7A patent/BR9811956B1/pt not_active IP Right Cessation
- 1998-08-13 EP EP98939941A patent/EP1003745B1/en not_active Expired - Lifetime
- 1998-08-13 ES ES98939941T patent/ES2235353T3/es not_active Expired - Lifetime
- 1998-08-13 DE DE69828408T patent/DE69828408T2/de not_active Expired - Lifetime
- 1998-08-13 KR KR1020007001710A patent/KR20010023089A/ko not_active Application Discontinuation
- 1998-08-13 NZ NZ502704A patent/NZ502704A/en unknown
- 1998-08-13 AU AU88289/98A patent/AU742999B2/en not_active Ceased
- 1998-08-19 ZA ZA987491A patent/ZA987491B/xx unknown
Also Published As
Publication number | Publication date |
---|---|
WO1999009030A1 (en) | 1999-02-25 |
DE69828408D1 (de) | 2005-02-03 |
AU8828998A (en) | 1999-03-08 |
EP1003745B1 (en) | 2004-12-29 |
AU742999B2 (en) | 2002-01-17 |
CA2291222A1 (en) | 1999-02-25 |
KR20010023089A (ko) | 2001-03-26 |
US6150359A (en) | 2000-11-21 |
NZ502704A (en) | 2002-06-28 |
ATE286053T1 (de) | 2005-01-15 |
CA2291222C (en) | 2004-03-30 |
JP2001515078A (ja) | 2001-09-18 |
BR9811956B1 (pt) | 2010-06-01 |
DE69828408T2 (de) | 2005-12-08 |
JP4965021B2 (ja) | 2012-07-04 |
BR9811956A (pt) | 2000-08-15 |
ES2235353T3 (es) | 2005-07-01 |
EP1003745A1 (en) | 2000-05-31 |
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