WO1999048868A3 - Heterocyclic classes of compounds for the modulating tyrosine protein kinase - Google Patents
Heterocyclic classes of compounds for the modulating tyrosine protein kinase Download PDFInfo
- Publication number
- WO1999048868A3 WO1999048868A3 PCT/US1999/006468 US9906468W WO9948868A3 WO 1999048868 A3 WO1999048868 A3 WO 1999048868A3 US 9906468 W US9906468 W US 9906468W WO 9948868 A3 WO9948868 A3 WO 9948868A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compounds
- protein kinase
- tyrosine protein
- modulating
- modulating tyrosine
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 title 1
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 title 1
- 229940100514 Syk tyrosine kinase inhibitor Drugs 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 title 1
- 238000000034 method Methods 0.000 abstract 3
- 102000001253 Protein Kinase Human genes 0.000 abstract 2
- 108060006633 protein kinase Proteins 0.000 abstract 2
- JVVRJMXHNUAPHW-UHFFFAOYSA-N 1h-pyrazol-5-amine Chemical compound NC=1C=CNN=1 JVVRJMXHNUAPHW-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- JYGFTBXVXVMTGB-UHFFFAOYSA-N indolin-2-one Chemical compound C1=CC=C2NC(=O)CC2=C1 JYGFTBXVXVMTGB-UHFFFAOYSA-N 0.000 abstract 1
- 230000019491 signal transduction Effects 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
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
- C07D403/02—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
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- 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
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- 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
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/86—Carbazoles; Hydrogenated carbazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU33635/99A AU3363599A (en) | 1998-03-26 | 1999-03-26 | Heterocyclic families of compounds for the modulation of tyrosine protein kinase |
| JP2000537851A JP2002507598A (en) | 1998-03-26 | 1999-03-26 | A family of heterocyclic compounds for regulating tyrosine protein kinase |
| CA002325935A CA2325935A1 (en) | 1998-03-26 | 1999-03-26 | Heterocyclic families of compounds for the modulation of tyrosine protein kinase |
| EP99915018A EP1066257A2 (en) | 1998-03-26 | 1999-03-26 | Heterocylic classes of compounds for the modulating tyrosine protein kinase |
Applications Claiming Priority (14)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7971398P | 1998-03-26 | 1998-03-26 | |
| US8042298P | 1998-04-02 | 1998-04-02 | |
| US8179298P | 1998-04-15 | 1998-04-15 | |
| US8205698P | 1998-04-16 | 1998-04-16 | |
| US8939798P | 1998-06-15 | 1998-06-15 | |
| US8952198P | 1998-06-16 | 1998-06-16 | |
| US9878398P | 1998-09-01 | 1998-09-01 | |
| US60/082,056 | 1998-09-01 | ||
| US60/089,397 | 1998-09-01 | ||
| US60/080,422 | 1998-09-01 | ||
| US60/079,713 | 1998-09-01 | ||
| US60/081,792 | 1998-09-01 | ||
| US60/089,521 | 1998-09-01 | ||
| US60/098,783 | 1998-09-01 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| WO1999048868A2 WO1999048868A2 (en) | 1999-09-30 |
| WO1999048868A3 true WO1999048868A3 (en) | 2000-02-24 |
| WO1999048868A9 WO1999048868A9 (en) | 2000-04-20 |
Family
ID=27568389
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US1999/006468 WO1999048868A2 (en) | 1998-03-26 | 1999-03-26 | Heterocyclic classes of compounds for the modulating tyrosine protein kinase |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1066257A2 (en) |
| JP (1) | JP2002507598A (en) |
| AU (1) | AU3363599A (en) |
| CA (1) | CA2325935A1 (en) |
| WO (1) | WO1999048868A2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7214700B2 (en) | 2000-05-02 | 2007-05-08 | Sugen Inc. | (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
| EA005032B1 (en) | 1998-05-29 | 2004-10-28 | Сьюджен, Инк. | Pyrrole substituted 2-indolinone (variants), pharmaceutical composition (variants), method for modulation of catalytic activity method for treating and preventing a protein kinase related disorders in an organism |
| TR200101860T2 (en) | 1998-12-17 | 2001-12-21 | F.Hoffmann-La Roche Ag | 4-alkenyl (and alkynyl) oxidols as cyclin-dependent kinase inhibitors |
| WO2000035921A1 (en) | 1998-12-17 | 2000-06-22 | F. Hoffmann-La Roche Ag | 4,5-pyrazinoxindoles as protein kinase inhibitors |
| US6153634A (en) * | 1998-12-17 | 2000-11-28 | Hoffmann-La Roche Inc. | 4,5-azolo-oxindoles |
| AU760039B2 (en) | 1998-12-17 | 2003-05-08 | F. Hoffmann-La Roche Ag | 4-aryloxindoles as inhibitors of JNK protein kinases |
| ATE494388T1 (en) | 1999-01-13 | 2011-01-15 | Univ New York State Res Found | NEW METHOD FOR CREATING PROTEIN KINASE INHIBITORS |
| US6878733B1 (en) | 1999-11-24 | 2005-04-12 | Sugen, Inc. | Formulations for pharmaceutical agents ionizable as free acids or free bases |
| WO2001037820A2 (en) * | 1999-11-24 | 2001-05-31 | Sugen, Inc. | Ionizable indolinone derivatives and their use as ptk ligands |
| US6313310B1 (en) | 1999-12-15 | 2001-11-06 | Hoffmann-La Roche Inc. | 4-and 5-alkynyloxindoles and 4-and 5-alkenyloxindoles |
| EP1255536B1 (en) * | 1999-12-22 | 2006-06-28 | Sugen, Inc. | Indolinone derivatives for modulation of c-kit tyrosine protein kinase |
| EP1259234B9 (en) * | 1999-12-30 | 2007-02-14 | Sugen, Inc. | 3-heteroarylidenyl-2-indolinone compounds for modulating protein kinase activity and for use in cancer chemotherapy |
| JP3663382B2 (en) | 2000-02-15 | 2005-06-22 | スージェン・インコーポレーテッド | Pyrrole-substituted 2-indolinone protein kinase inhibitor |
| GB0010757D0 (en) | 2000-05-05 | 2000-06-28 | Astrazeneca Ab | Chemical compounds |
| AR042586A1 (en) | 2001-02-15 | 2005-06-29 | Sugen Inc | 3- (4-AMIDOPIRROL-2-ILMETILIDEN) -2-INDOLINONE AS INHIBITORS OF PROTEIN KINASE; YOUR PHARMACEUTICAL COMPOSITIONS; A METHOD FOR THE MODULATION OF THE CATALYTIC ACTIVITY OF PROTEINQUINASE; A METHOD TO TREAT OR PREVENT AN AFFECTION RELATED TO PROTEINQUINASE |
| US7186745B2 (en) | 2001-03-06 | 2007-03-06 | Astrazeneca Ab | Indolone derivatives having vascular damaging activity |
| WO2002094809A1 (en) * | 2001-05-24 | 2002-11-28 | Yamanouchi Pharmaceutical Co., Ltd. | 3-quinoline-2-(1h)-ylideneindolin-2-one derivatives |
| GB0121941D0 (en) | 2001-09-11 | 2001-10-31 | Astrazeneca Ab | Chemical compounds |
| US7005445B2 (en) | 2001-10-22 | 2006-02-28 | The Research Foundation Of State University Of New York | Protein kinase and phosphatase inhibitors and methods for designing them |
| US20030119839A1 (en) * | 2001-12-13 | 2003-06-26 | Nan-Horng Lin | Protein kinase inhibitors |
| WO2003070725A2 (en) | 2002-02-15 | 2003-08-28 | Pharmacia & Upjohn Company | Process for preparing indolinone derivatives |
| US7825132B2 (en) | 2002-08-23 | 2010-11-02 | Novartis Vaccines And Diagnostics, Inc. | Inhibition of FGFR3 and treatment of multiple myeloma |
| WO2004043389A2 (en) | 2002-11-13 | 2004-05-27 | Chiron Corporation | Methods of treating cancer and related methods |
| WO2004048366A1 (en) * | 2002-11-22 | 2004-06-10 | Yamanouchi Pharmaceutical Co., Ltd. | 2-oxoindoline derivatives |
| US20050043233A1 (en) | 2003-04-29 | 2005-02-24 | Boehringer Ingelheim International Gmbh | Combinations for the treatment of diseases involving cell proliferation, migration or apoptosis of myeloma cells or angiogenesis |
| EP1718306A2 (en) | 2004-02-20 | 2006-11-08 | Chiron Corporation | Modulation of inflammatory and metastatic processes |
| GT200500321A (en) * | 2004-11-09 | 2006-09-04 | COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF PROTEIN KINASE. | |
| MX2007014782A (en) | 2005-05-23 | 2008-02-19 | Novartis Ag | Crystalline and other forms of 4-amino-5-fluoro-3-[6-(4- methylpiperazin-1-yl)-1h-benzimidazol-2-yl]-1h-quinolin-2-one lactic acid salts. |
| RU2430913C2 (en) | 2006-01-06 | 2011-10-10 | Сепракор Инк. | Cycloalkylamines as monoamine reuptake inhibitors |
| CN104276955A (en) | 2006-01-06 | 2015-01-14 | 赛诺维信制药公司 | Tetralone-based monoamine reuptake inhibitors |
| PT2816024T (en) | 2006-03-31 | 2017-10-20 | Sunovion Pharmaceuticals Inc | Chiral amines |
| US7838542B2 (en) | 2006-06-29 | 2010-11-23 | Kinex Pharmaceuticals, Llc | Bicyclic compositions and methods for modulating a kinase cascade |
| US7884124B2 (en) | 2006-06-30 | 2011-02-08 | Sepracor Inc. | Fluoro-substituted inhibitors of D-amino acid oxidase |
| JP4937881B2 (en) * | 2006-11-01 | 2012-05-23 | 財団法人工業技術研究院 | Azulene compounds |
| WO2008089453A2 (en) | 2007-01-18 | 2008-07-24 | Sepracor Inc. | Inhibitors of d-amino acid oxidase |
| US7902252B2 (en) | 2007-01-18 | 2011-03-08 | Sepracor, Inc. | Inhibitors of D-amino acid oxidase |
| 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 |
| NZ580429A (en) | 2007-05-31 | 2012-04-27 | Sepracor Inc | Phenyl substituted cycloalkylamines as monoamine reuptake inhibitors |
| PL2197280T3 (en) | 2007-08-27 | 2013-11-29 | Basf Se | Pyrazole compounds for controlling invertebrate pests |
| AU2008326381B2 (en) * | 2007-11-21 | 2014-10-23 | Decode Genetics Ehf | Biaryl PDE4 inhibitors for treating inflammation |
| ES2710701T3 (en) | 2008-09-24 | 2019-04-26 | Basf Se | Pyrazole compounds for the control of invertebrate pests |
| PL2342196T3 (en) | 2008-09-24 | 2015-12-31 | Basf Se | Pyrazole compounds for controlling invertebrate pests |
| EP2451808B1 (en) | 2009-07-06 | 2014-03-26 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
| WO2011003796A1 (en) | 2009-07-06 | 2011-01-13 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
| JP2013500246A (en) | 2009-07-24 | 2013-01-07 | ビーエーエスエフ ソシエタス・ヨーロピア | Pyridine derivative compounds for invertebrate pest control |
| US8569331B2 (en) | 2010-11-01 | 2013-10-29 | Arqule, Inc. | Substituted benzo[f]lmidazo[1,2-d]pyrido[2,3-b][1,4]diazepine compounds |
Citations (12)
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|---|---|---|---|---|
| WO1991013055A2 (en) * | 1990-02-28 | 1991-09-05 | Farmitalia Carlo Erba S.R.L. | New aryl- and heteroarylethenylene derivatives and process for their preparation |
| WO1992007830A2 (en) * | 1990-10-29 | 1992-05-14 | Pfizer Inc. | Oxindole peptide antagonists |
| WO1992020642A1 (en) * | 1991-05-10 | 1992-11-26 | Rhone-Poulenc Rorer International (Holdings) Inc. | Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit egf and/or pdgf receptor tyrosine kinase |
| WO1994014808A1 (en) * | 1992-12-23 | 1994-07-07 | Farmitalia Carlo Erba Srl | Vinylene-azaindole derivatives and process for their preparation |
| WO1995024190A2 (en) * | 1994-03-07 | 1995-09-14 | Sugen, Inc. | Receptor tyrosine kinase inhibitors for inhibiting cell proliferative disorders and compositions thereof |
| WO1996000226A1 (en) * | 1994-06-24 | 1996-01-04 | Pharmacia S.P.A. | Substituted azaindolylidene compounds and process for their preparation |
| WO1996016964A1 (en) * | 1994-11-28 | 1996-06-06 | Pharmacia & Upjohn S.P.A | Substituted 3-arylidene-7-azaoxindole compounds and process for their preparation |
| WO1996040116A1 (en) * | 1995-06-07 | 1996-12-19 | Sugen, Inc. | Indolinone compounds for the treatment of disease |
| WO1998007695A1 (en) * | 1996-08-23 | 1998-02-26 | Sugen, Inc. | Indolinone combinatorial libraries and related products and methods for the treatment of disease |
| WO1998045708A1 (en) * | 1997-04-08 | 1998-10-15 | Sugen, Inc. | Study and treatment of diseases related to specific cellular functions of receptor protein tyrosine kinases |
| WO1998050356A1 (en) * | 1997-05-07 | 1998-11-12 | Sugen, Inc. | 2-indolinone derivatives as modulators of protein kinase activity |
| WO1998056376A1 (en) * | 1997-06-13 | 1998-12-17 | Sugen, Inc. | Novel heteroaryl compounds for the modulation of protein tyrosine enzyme related cellular signal transduction |
-
1999
- 1999-03-26 EP EP99915018A patent/EP1066257A2/en not_active Withdrawn
- 1999-03-26 CA CA002325935A patent/CA2325935A1/en not_active Abandoned
- 1999-03-26 AU AU33635/99A patent/AU3363599A/en not_active Abandoned
- 1999-03-26 JP JP2000537851A patent/JP2002507598A/en not_active Withdrawn
- 1999-03-26 WO PCT/US1999/006468 patent/WO1999048868A2/en active Search and Examination
Patent Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991013055A2 (en) * | 1990-02-28 | 1991-09-05 | Farmitalia Carlo Erba S.R.L. | New aryl- and heteroarylethenylene derivatives and process for their preparation |
| WO1992007830A2 (en) * | 1990-10-29 | 1992-05-14 | Pfizer Inc. | Oxindole peptide antagonists |
| WO1992020642A1 (en) * | 1991-05-10 | 1992-11-26 | Rhone-Poulenc Rorer International (Holdings) Inc. | Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit egf and/or pdgf receptor tyrosine kinase |
| WO1994014808A1 (en) * | 1992-12-23 | 1994-07-07 | Farmitalia Carlo Erba Srl | Vinylene-azaindole derivatives and process for their preparation |
| WO1995024190A2 (en) * | 1994-03-07 | 1995-09-14 | Sugen, Inc. | Receptor tyrosine kinase inhibitors for inhibiting cell proliferative disorders and compositions thereof |
| WO1996000226A1 (en) * | 1994-06-24 | 1996-01-04 | Pharmacia S.P.A. | Substituted azaindolylidene compounds and process for their preparation |
| WO1996016964A1 (en) * | 1994-11-28 | 1996-06-06 | Pharmacia & Upjohn S.P.A | Substituted 3-arylidene-7-azaoxindole compounds and process for their preparation |
| WO1996040116A1 (en) * | 1995-06-07 | 1996-12-19 | Sugen, Inc. | Indolinone compounds for the treatment of disease |
| WO1998007695A1 (en) * | 1996-08-23 | 1998-02-26 | Sugen, Inc. | Indolinone combinatorial libraries and related products and methods for the treatment of disease |
| WO1998045708A1 (en) * | 1997-04-08 | 1998-10-15 | Sugen, Inc. | Study and treatment of diseases related to specific cellular functions of receptor protein tyrosine kinases |
| WO1998050356A1 (en) * | 1997-05-07 | 1998-11-12 | Sugen, Inc. | 2-indolinone derivatives as modulators of protein kinase activity |
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| GAZIT,A. ET AL.: "Tyrphostins. 2. Heterocyclic and alpha-Substituted Benzylidenmalonitirle Tyrphostins as Poitent Inhibitors of EGRF Receptor and ErbB2/neu Tyrosine Kinases", J.MED.CHEM., vol. 34, no. 6, June 1991 (1991-06-01), WASHINGTON, pages 1896 - 1907, XP000472938 * |
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| SUN,LO. ET AL.: "Synthesis and Biological Evaluation of 3-Substituted Indolin-2-ones : A novel Class of Tyrosine Kinase Inhibitors That Exhibit Selectivity toward Particualr Receptor Tyrosine Kinases", J.MED.CHEM., vol. 41, no. 14, 2 July 1998 (1998-07-02), WASHINGTON, pages 2588 - 2603, XP002122185 * |
| TRAXLER,P.M.: "Protein tyrosine kinase inhibitors in cancer treatment", EXP.OPIN.THER.PATENTS, vol. 7, no. 6, 1997, LONDON, pages 571 - 588, XP002122590 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7214700B2 (en) | 2000-05-02 | 2007-05-08 | Sugen Inc. | (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1066257A2 (en) | 2001-01-10 |
| WO1999048868A9 (en) | 2000-04-20 |
| WO1999048868A2 (en) | 1999-09-30 |
| AU3363599A (en) | 1999-10-18 |
| CA2325935A1 (en) | 1999-09-30 |
| JP2002507598A (en) | 2002-03-12 |
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