WO2002055517A3 - 4-(hetero)aryl substituted indolinones - Google Patents
4-(hetero)aryl substituted indolinones Download PDFInfo
- Publication number
- WO2002055517A3 WO2002055517A3 PCT/US2001/048564 US0148564W WO02055517A3 WO 2002055517 A3 WO2002055517 A3 WO 2002055517A3 US 0148564 W US0148564 W US 0148564W WO 02055517 A3 WO02055517 A3 WO 02055517A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hetero
- aryl substituted
- formula
- protein kinase
- relates
- Prior art date
Links
Classifications
-
- 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
- C07D403/14—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 three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/16—Central respiratory analeptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- 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
- 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
- C07D403/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D417/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Abstract
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002556186A JP2004518669A (en) | 2000-12-20 | 2001-12-20 | 4-Aryl substituted indolinone |
EP01997065A EP1349852A2 (en) | 2000-12-20 | 2001-12-20 | 4-(hetero)aryl substituted indolinones |
CA002432114A CA2432114A1 (en) | 2000-12-20 | 2001-12-20 | 4-(hetero)aryl substituted indolinones |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25647900P | 2000-12-20 | 2000-12-20 | |
US60/256,479 | 2000-12-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2002055517A2 WO2002055517A2 (en) | 2002-07-18 |
WO2002055517A3 true WO2002055517A3 (en) | 2002-09-26 |
Family
ID=22972383
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2001/048564 WO2002055517A2 (en) | 2000-12-20 | 2001-12-20 | 4-(hetero)aryl substituted indolinones |
Country Status (7)
Country | Link |
---|---|
US (2) | US6677368B2 (en) |
EP (1) | EP1349852A2 (en) |
JP (1) | JP2004518669A (en) |
AR (1) | AR035721A1 (en) |
CA (1) | CA2432114A1 (en) |
PE (1) | PE20020776A1 (en) |
WO (1) | WO2002055517A2 (en) |
Families Citing this family (55)
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US6316429B1 (en) * | 1997-05-07 | 2001-11-13 | Sugen, Inc. | Bicyclic protein kinase inhibitors |
US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
ES2290117T3 (en) * | 2000-02-15 | 2008-02-16 | Sugen, Inc. | PROTEIN QUINASE 2-INDOLIN INHIBITORS REPLACED WITH PIRROL. |
WO2001094312A2 (en) * | 2000-06-02 | 2001-12-13 | Sugen, Inc. | Indolinone derivatives as protein kinase/phosphatase inhibitors |
CA2452368A1 (en) | 2001-06-29 | 2003-01-09 | Ab Science | New potent, selective and non toxic c-kit inhibitors |
US20040266797A1 (en) * | 2001-06-29 | 2004-12-30 | Alain Moussy | Use of potent,selective and non toxic c-kit inhibitors for treating tumor angiogensis |
CA2452371A1 (en) | 2001-06-29 | 2003-01-09 | Ab Science | Use of tyrosine kinase inhibitors for treating allergic diseases |
DE60212627T2 (en) | 2001-06-29 | 2007-06-14 | Ab Science | Use of tyrosine kinase inhibitors for the treatment of inflammatory diseases |
US7678805B2 (en) | 2001-06-29 | 2010-03-16 | Ab Science | Use of tyrosine kinase inhibitors for treating inflammatory bowel diseases (IBD) |
US20090197852A9 (en) * | 2001-08-06 | 2009-08-06 | Johnson Robert G Jr | Method of treating breast cancer using 17-AAG or 17-AG or a prodrug of either in combination with a HER2 inhibitor |
BR0213185A (en) * | 2001-10-10 | 2004-09-14 | Sugen Inc | 3- [4- (Substituted Heterocyclyl) -pyrrol-2-ylmethylidene] 2-indolinone derivatives as kinase inhibitors |
TWI259081B (en) * | 2001-10-26 | 2006-08-01 | Sugen Inc | Treatment of acute myeloid leukemia with indolinone compounds |
US20030119839A1 (en) * | 2001-12-13 | 2003-06-26 | Nan-Horng Lin | Protein kinase inhibitors |
US6686362B2 (en) | 2001-12-27 | 2004-02-03 | Theravance, Inc. | Indolinone derivatives |
TWI329105B (en) * | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
DE10209520A1 (en) * | 2002-03-04 | 2003-09-25 | 4Sc Ag | New modulators of potassium channels |
GB0217757D0 (en) * | 2002-07-31 | 2002-09-11 | Glaxo Group Ltd | Novel compounds |
US20050032871A1 (en) * | 2002-09-03 | 2005-02-10 | Sugen, Inc. | Sulfonylated pyrrole-2-indolinone derivatives as kinase inhibitors |
WO2004113304A1 (en) * | 2003-05-22 | 2004-12-29 | Abbott Laboratories | Indazole, benzisoxazole, and benzisothiazole kinase inhibitors |
US7297709B2 (en) | 2003-05-22 | 2007-11-20 | Abbott Laboratories | Indazole, benzisoxazole, and benzisothiazole kinase inhibitors |
NZ543709A (en) * | 2003-05-27 | 2009-04-30 | Robert Per Hagerkvist | Use of tyrosine kinase inhibitor to treat diabetes |
NZ545270A (en) | 2003-07-30 | 2010-04-30 | Rigel Pharmaceuticals Inc | 2,4-Pyrimidinediamine compounds for use in the treatment or prevention of autoimmune diseases |
US7504401B2 (en) | 2003-08-29 | 2009-03-17 | Locus Pharmaceuticals, Inc. | Anti-cancer agents and uses thereof |
US7160876B2 (en) | 2003-12-22 | 2007-01-09 | Abbott Laboratories | Fused bicycloheterocycle substituted quinuclidine derivatives |
GB0402143D0 (en) * | 2004-01-30 | 2004-03-03 | Smithkline Beecham Corp | Novel compounds |
US20100267719A1 (en) * | 2005-05-26 | 2010-10-21 | The Scripps Research Institute | Enhanced Indolinone Based Protein Kinase Inhibitors |
ES2651349T3 (en) | 2005-06-08 | 2018-01-25 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibiting the JAK route |
US20070203161A1 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
ES2426448T3 (en) | 2006-01-27 | 2013-10-23 | Shanghai Hengrui Pharmaceutical Co. Ltd. | Pyrrolo [3,2-c] pyridin-4-one 2-indolinone protein kinase inhibitors |
JP2009528295A (en) * | 2006-02-24 | 2009-08-06 | ライジェル ファーマシューティカルズ, インコーポレイテッド | Compositions and methods for inhibition of the JAK pathway |
MX2008011127A (en) * | 2006-03-02 | 2008-10-31 | Astellas Pharma Inc | 17β HSD type 5 INHIBITOR. |
EP1829862A1 (en) * | 2006-03-02 | 2007-09-05 | Laboratorios Del Dr. Esteve, S.A. | Sigma receptor compounds |
CA2644910C (en) * | 2006-03-31 | 2014-01-28 | Abbott Laboratories | Indazole compounds |
WO2008033743A1 (en) | 2006-09-11 | 2008-03-20 | Curis, Inc. | Substituted 2-indolinone as ptk inhibitors containing a zinc binding moiety |
ES2565683T3 (en) * | 2006-09-15 | 2016-04-06 | Xcovery, Inc. | Kinase Inhibitor Compounds |
RU2009116818A (en) * | 2006-10-06 | 2010-11-20 | Айрм Ллк (Bm) | PROTEINKINASE INHIBITORS AND WAYS OF THEIR APPLICATION |
EP1918277B1 (en) * | 2006-11-01 | 2015-06-10 | Industrial Technology Research Institute | Azulene compounds |
WO2008138184A1 (en) * | 2007-05-14 | 2008-11-20 | Shanghai Hengrui Pharmaceutical Co.Ltd. | Derivatives of pyrroloazacycles, the method of making them and the use thereof as inhibitors of protein kinases |
KR101700454B1 (en) | 2008-02-15 | 2017-01-26 | 리겔 파마슈티칼스, 인크. | Pyrimidine-2-amine compounds and their use as inhibitors of jak kinases |
US8138339B2 (en) | 2008-04-16 | 2012-03-20 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
US8063058B2 (en) | 2008-04-16 | 2011-11-22 | Portola Pharmaceuticals, Inc. | Inhibitors of syk and JAK protein kinases |
BRPI0910668A2 (en) * | 2008-04-22 | 2019-09-24 | Portola Pharmaceutiacals Inc | protein kinase inhibitors |
US8829039B2 (en) | 2008-05-23 | 2014-09-09 | Shanghai Institute Of Pharmaceutical Industry | Dihydroindolinone derivatives |
US7897602B2 (en) * | 2009-01-12 | 2011-03-01 | Development Center For Biotechnology | Indolinone compounds as kinase inhibitors |
JP5738292B2 (en) * | 2009-07-28 | 2015-06-24 | ライジェル ファーマシューティカルズ, インコーポレイテッド | Compositions and methods for inhibition of the JAK pathway |
CN102276584A (en) * | 2010-06-08 | 2011-12-14 | 齐鲁制药有限公司 | Pyrrole-substituted 2-dihydroindolone derivative and preparation method and application thereof |
EP2635557A2 (en) | 2010-11-01 | 2013-09-11 | Portola Pharmaceuticals, Inc. | Nicotinamides as jak kinase modulators |
KR102019530B1 (en) | 2011-11-23 | 2019-09-06 | 포톨라 파마슈티컬스, 인코포레이티드 | Pyrazine kinase inhibitors |
EP2903970A4 (en) | 2012-10-08 | 2016-11-30 | Portola Pharm Inc | Substituted pyrimidinyl kinase inhibitors |
CN105408320B (en) * | 2013-03-13 | 2019-08-13 | 北京强新生物科技有限公司 | 3- (aryl or heteroaryl) methyl indol -2- ketone derivatives as cancer stem cell approach kinase inhibitor for treating cancer |
CN103274986A (en) * | 2013-06-20 | 2013-09-04 | 湖南欧亚生物有限公司 | Method for synthetising and refining sunitinib intermediate |
CN104829596B (en) * | 2014-02-10 | 2017-02-01 | 石家庄以岭药业股份有限公司 | Pyrrole-substituted indolinone derivative and preparation method thereof, composition including derivative, and application of derivative |
US11427591B2 (en) * | 2018-10-17 | 2022-08-30 | Insilico Medicine Ip Limited | Kinase inhibitors |
WO2023168246A2 (en) * | 2022-03-01 | 2023-09-07 | Purdue Research Foundation | Selective g protein-coupled receptor kinase 5 inhibitors, compositions, and methods of use |
CN114853736B (en) * | 2022-07-06 | 2022-10-21 | 北京鑫开元医药科技有限公司 | Compound with TRK inhibitory activity, preparation method, composition and application thereof |
Citations (11)
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US5792783A (en) * | 1995-06-07 | 1998-08-11 | Sugen, Inc. | 3-heteroaryl-2-indolinone compounds for the treatment of disease |
WO1998050356A1 (en) * | 1997-05-07 | 1998-11-12 | Sugen, Inc. | 2-indolinone derivatives as modulators of protein kinase activity |
WO1999061422A1 (en) * | 1998-05-29 | 1999-12-02 | Sugen, Inc. | Pyrrole substituted 2-indolinone protein kinase inhibitors |
WO2000008202A2 (en) * | 1998-08-04 | 2000-02-17 | Sugen, Inc. | 3-methylidenyl-2-indolinone modulators of protein kinase |
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WO2000035908A1 (en) * | 1998-12-17 | 2000-06-22 | F. Hoffmann-La Roche Ag | 4-alkenyl (and alkynyl) oxindoles as inhibitors of cyclin-dependent kinases, in particular cdk2 |
US6114371A (en) * | 1997-06-20 | 2000-09-05 | Sugen, Inc. | 3-(cyclohexanoheteroarylidenyl)-2-indolinone protein tyrosine kinase inhibitors |
US6147106A (en) * | 1997-08-20 | 2000-11-14 | Sugen, Inc. | Indolinone combinatorial libraries and related products and methods for the treatment of disease |
WO2001049287A1 (en) * | 1999-12-30 | 2001-07-12 | Sugen, Inc. | 3-heteroarylidenyl-2-indolinone compounds for modulating protein kinase activity and for use in cancer chemotherapy |
WO2001094312A2 (en) * | 2000-06-02 | 2001-12-13 | Sugen, Inc. | Indolinone derivatives as protein kinase/phosphatase inhibitors |
WO2002002551A1 (en) * | 2000-06-30 | 2002-01-10 | Sugen, Inc. | 4-heteroaryl-3-heteroarylidenyl-2-indolinones and their use as protein kinase inhibitors |
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EP0654024A1 (en) * | 1992-08-06 | 1995-05-24 | Warner-Lambert Company | 2-thioindoles (selenoindoles) and related disulfides (selenides) which inhibit protein tyrosine kinases and which have antitumor properties |
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US6028850A (en) * | 1998-07-10 | 2000-02-22 | Hyundai Electronics America, Inc. | Wireless transceiver and frequency plan |
EP1233943B1 (en) * | 1999-11-24 | 2011-06-29 | Sugen, Inc. | Ionizable indolinone derivatives and their use as ptk ligands |
ES2290117T3 (en) * | 2000-02-15 | 2008-02-16 | Sugen, Inc. | PROTEIN QUINASE 2-INDOLIN INHIBITORS REPLACED WITH PIRROL. |
-
2001
- 2001-12-20 AR ARP010105973A patent/AR035721A1/en unknown
- 2001-12-20 WO PCT/US2001/048564 patent/WO2002055517A2/en not_active Application Discontinuation
- 2001-12-20 CA CA002432114A patent/CA2432114A1/en not_active Abandoned
- 2001-12-20 US US10/023,488 patent/US6677368B2/en not_active Expired - Fee Related
- 2001-12-20 PE PE2001001289A patent/PE20020776A1/en not_active Application Discontinuation
- 2001-12-20 EP EP01997065A patent/EP1349852A2/en not_active Withdrawn
- 2001-12-20 JP JP2002556186A patent/JP2004518669A/en active Pending
-
2003
- 2003-12-16 US US10/736,243 patent/US6861418B2/en not_active Expired - Fee Related
Patent Citations (11)
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US5792783A (en) * | 1995-06-07 | 1998-08-11 | Sugen, Inc. | 3-heteroaryl-2-indolinone compounds for the treatment of disease |
WO1998050356A1 (en) * | 1997-05-07 | 1998-11-12 | Sugen, Inc. | 2-indolinone derivatives as modulators of protein kinase activity |
US6114371A (en) * | 1997-06-20 | 2000-09-05 | Sugen, Inc. | 3-(cyclohexanoheteroarylidenyl)-2-indolinone protein tyrosine kinase inhibitors |
US6147106A (en) * | 1997-08-20 | 2000-11-14 | Sugen, Inc. | Indolinone combinatorial libraries and related products and methods for the treatment of disease |
WO1999061422A1 (en) * | 1998-05-29 | 1999-12-02 | Sugen, Inc. | Pyrrole substituted 2-indolinone protein kinase inhibitors |
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WO2000035909A1 (en) * | 1998-12-17 | 2000-06-22 | F. Hoffmann-La Roche Ag | 4-aryloxindoles as inhibitors of jnk protein kinases |
WO2000035908A1 (en) * | 1998-12-17 | 2000-06-22 | F. Hoffmann-La Roche Ag | 4-alkenyl (and alkynyl) oxindoles as inhibitors of cyclin-dependent kinases, in particular cdk2 |
WO2001049287A1 (en) * | 1999-12-30 | 2001-07-12 | Sugen, Inc. | 3-heteroarylidenyl-2-indolinone compounds for modulating protein kinase activity and for use in cancer chemotherapy |
WO2001094312A2 (en) * | 2000-06-02 | 2001-12-13 | Sugen, Inc. | Indolinone derivatives as protein kinase/phosphatase inhibitors |
WO2002002551A1 (en) * | 2000-06-30 | 2002-01-10 | Sugen, Inc. | 4-heteroaryl-3-heteroarylidenyl-2-indolinones and their use as protein kinase inhibitors |
Also Published As
Publication number | Publication date |
---|---|
US6861418B2 (en) | 2005-03-01 |
WO2002055517A2 (en) | 2002-07-18 |
PE20020776A1 (en) | 2002-08-22 |
US20030069297A1 (en) | 2003-04-10 |
US6677368B2 (en) | 2004-01-13 |
AR035721A1 (en) | 2004-07-07 |
JP2004518669A (en) | 2004-06-24 |
US20040157909A1 (en) | 2004-08-12 |
EP1349852A2 (en) | 2003-10-08 |
CA2432114A1 (en) | 2002-07-18 |
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