CA2383623A1 - Modulateurs 3-methylidenyl-2-indolinone de proteine kinase - Google Patents
Modulateurs 3-methylidenyl-2-indolinone de proteine kinase Download PDFInfo
- Publication number
- CA2383623A1 CA2383623A1 CA002383623A CA2383623A CA2383623A1 CA 2383623 A1 CA2383623 A1 CA 2383623A1 CA 002383623 A CA002383623 A CA 002383623A CA 2383623 A CA2383623 A CA 2383623A CA 2383623 A1 CA2383623 A1 CA 2383623A1
- Authority
- CA
- Canada
- Prior art keywords
- dihydroindol
- indol
- group
- oxo
- methoxybenzylidene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
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
- C07D401/10—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 carbon chain containing aromatic rings
-
- 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
- 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
-
- 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
-
- 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
- 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
- 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
- C07D405/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D409/10—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 aromatic rings
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
L'invention concerne de nouveaux composés 3-méthylidényl-2-indolinone ainsi que leurs sels physiologiquement acceptables et leurs promédicaments. Ces composés modulent l'activité des protéines kinases et par conséquent sont supposés convenir à la prévention et au traitement des troubles cellulaires liés à la protéine kinase, comme par exemple le cancer.
Applications Claiming Priority (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12925698A | 1998-08-04 | 1998-08-04 | |
US9547098P | 1998-08-05 | 1998-08-05 | |
US10217898P | 1998-09-28 | 1998-09-28 | |
US11610799P | 1999-01-15 | 1999-01-15 | |
US60/116,107 | 1999-01-15 | ||
US60/095,470 | 1999-01-15 | ||
US09/129,256 | 1999-01-15 | ||
US60/102,178 | 1999-01-15 | ||
PCT/US1999/017845 WO2000008202A2 (fr) | 1998-08-04 | 1999-08-04 | Modulateurs 3-methylidenyl-2-indolinone de proteine kinase |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2383623A1 true CA2383623A1 (fr) | 2000-02-17 |
Family
ID=27492796
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002383623A Abandoned CA2383623A1 (fr) | 1998-08-04 | 1999-08-04 | Modulateurs 3-methylidenyl-2-indolinone de proteine kinase |
Country Status (4)
Country | Link |
---|---|
JP (1) | JP2002522452A (fr) |
AU (1) | AU5468499A (fr) |
CA (1) | CA2383623A1 (fr) |
WO (1) | WO2000008202A2 (fr) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009079767A1 (fr) * | 2007-12-21 | 2009-07-02 | University Health Network | Dérivés d'indolmone à substitution indazolyle, benzimidazolyle, benzotriazolyle en tant qu'inhibiteurs de kinases utilisés dans le traitement du cancer |
WO2010115279A1 (fr) * | 2009-04-06 | 2010-10-14 | University Health Network | Inhibiteurs de kinases et procédé de traitement du cancer avec ceux-ci |
WO2012048411A1 (fr) * | 2010-10-13 | 2012-04-19 | University Health Network | Inhibiteurs de plk4 et méthode de traitement du cancer à l'aide de ceux-ci |
US8263596B2 (en) | 2010-04-06 | 2012-09-11 | University Health Network | Kinase inhibitors and method of treating cancer |
US20160250220A1 (en) | 2013-10-18 | 2016-09-01 | University Health Network | Treatment for pancreatic cancer |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6569868B2 (en) | 1998-04-16 | 2003-05-27 | Sugen, Inc. | 2-indolinone derivatives as modulators of protein kinase activity |
TR200101756T2 (tr) | 1998-12-17 | 2001-10-22 | F.Hoffmann-La Roche Ag | Protein kinaz inhibitörleri olarak 4,5-pirazinoksindoller. |
US6153634A (en) | 1998-12-17 | 2000-11-28 | Hoffmann-La Roche Inc. | 4,5-azolo-oxindoles |
KR20010101266A (ko) | 1998-12-17 | 2001-11-14 | 프리돌린 클라우스너, 롤란드 비. 보레르 | Jnk 단백질 키나제의 억제제로서의 4-아릴옥신돌 |
ES2192877T3 (es) * | 1998-12-17 | 2003-10-16 | Hoffmann La Roche | 4-alquenil (y alquinil) oxindoles como inhibidores de kinasas ciclina-dependientes, en particular cdk2. |
AU1928501A (en) * | 1999-11-24 | 2001-06-04 | Sugen, Inc. | Formulations for pharmaceutical agents ionizable as free acids or free bases |
US6878733B1 (en) | 1999-11-24 | 2005-04-12 | Sugen, Inc. | Formulations for pharmaceutical agents ionizable as free acids or free bases |
US6313310B1 (en) | 1999-12-15 | 2001-11-06 | Hoffmann-La Roche Inc. | 4-and 5-alkynyloxindoles and 4-and 5-alkenyloxindoles |
MXPA02010759A (es) | 2000-05-02 | 2004-07-30 | Sugen Inc | Derivados del acido (2-oxindol-3-ilidenil) acetico y su uso como inhibidores de la proteina quinasa. |
MY128450A (en) * | 2000-05-24 | 2007-02-28 | Upjohn Co | 1-(pyrrolidin-1-ylmethyl)-3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives |
WO2001094312A2 (fr) * | 2000-06-02 | 2001-12-13 | Sugen, Inc. | Derives d'indolinone comme inhibiteurs de phosphatase/proteine kinase |
US6677368B2 (en) * | 2000-12-20 | 2004-01-13 | Sugen, Inc. | 4-aryl substituted indolinones |
JP2004529110A (ja) | 2001-03-06 | 2004-09-24 | アストラゼネカ アクチボラグ | 脈管損傷活性を有するインドール誘導体 |
US7081454B2 (en) | 2001-03-28 | 2006-07-25 | Bristol-Myers Squibb Co. | Tyrosine kinase inhibitors |
WO2002081466A1 (fr) * | 2001-04-09 | 2002-10-17 | Sugen, Inc. | Promedicaments a base de derives 3-(pyrrol-2-ylmethylidene)-2-indolinone |
JPWO2002094809A1 (ja) * | 2001-05-24 | 2004-09-09 | 山之内製薬株式会社 | 3−キノリン−2(1h)−イリデンインドリン−2−オン誘導体 |
PE20030062A1 (es) | 2001-05-30 | 2003-02-08 | Sugen Inc | Derivados aralquilsulfonil-3-(pirrol-2-ilmetiliden)-2-indolinona como inhibidores de quinasas |
US6777417B2 (en) | 2001-09-10 | 2004-08-17 | Sugen, Inc. | 3-(4,5,6,7-tetrahydroindol-2-ylmethylidiene-2-indolinone derivatives as kinase inhibitors |
ES2275021T3 (es) | 2001-09-27 | 2007-06-01 | Smithkline Beecham Corporation | Derivados de azoxoindol como inhibidores de trk proteina quinasa para el tratamiento de cancer y dolor cronico. |
WO2004048366A1 (fr) * | 2002-11-22 | 2004-06-10 | Yamanouchi Pharmaceutical Co., Ltd. | Derives 2-oxoindoline |
JP4879492B2 (ja) * | 2002-11-27 | 2012-02-22 | アラーガン、インコーポレイテッド | 疾患の治療のためのキナーゼ阻害剤 |
US7517697B2 (en) * | 2003-02-05 | 2009-04-14 | Applied Biosystems, Llc | Compositions and methods for preserving RNA in biological samples |
US7312215B2 (en) | 2003-07-29 | 2007-12-25 | Bristol-Myers Squibb Company | Benzimidazole C-2 heterocycles as kinase inhibitors |
GT200500321A (es) * | 2004-11-09 | 2006-09-04 | Compuestos y composiciones como inhibidores de proteina kinase. | |
WO2006119148A2 (fr) * | 2005-04-29 | 2006-11-09 | The Ohio State University Research Foundation | Inhibiteurs specifiques contre la tyrosine du recepteur du facteur de croissance des keratinocytes utiles pour prevenir les metastases cancereuses |
WO2009030270A1 (fr) * | 2007-09-03 | 2009-03-12 | Novartis Ag | Dérivés dhydroindoles utilisés pour traiter la maladie de parkinson |
FR2948940B1 (fr) * | 2009-08-04 | 2011-07-22 | Servier Lab | Nouveaux derives dihydroindolones, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
WO2012142029A2 (fr) * | 2011-04-10 | 2012-10-18 | Florida A&M University | Modulateurs sélectifs des récepteurs des œstrogènes pour traitement de troubles à médiation par les récepteurs des œstrogènes |
CN104619701B (zh) | 2012-09-13 | 2016-10-19 | 霍夫曼-拉罗奇有限公司 | 用于治疗cns疾病的2-氧代-2,3-二氢-吲哚类化合物 |
WO2014066840A1 (fr) | 2012-10-26 | 2014-05-01 | Regents Of The University Of Minnesota | Inhibiteurs d'aurora kinase |
CA3004595A1 (fr) * | 2015-11-12 | 2017-05-18 | Lg Chem, Ltd. | Composition pharmaceutique contenant, en tant que principe actif, un derive ou un sel pharmaceutiquement acceptable de 7-azaindolin-2-one |
US10487054B2 (en) | 2017-04-21 | 2019-11-26 | Regents Of The University Of Minnesota | Therapeutic compounds |
SG11202103459WA (en) * | 2018-10-05 | 2021-05-28 | Ichnos Sciences S A | Indolinone compounds for use as map4k1 inhibitors |
GR1010103B (el) * | 2020-07-02 | 2021-10-18 | Uni-Pharma Κλεων Τσετης Φαρμακευτικα Εργαστηρια Αβεε, | 3-ινδολ-2-υλομεθυλιδενο-ινδολιν-2-ονες με δραση αναστολης της αυτοταξινης |
WO2022006412A2 (fr) * | 2020-07-02 | 2022-01-06 | The Regents Of The University Of Colorado, A Body Corporate | Conjugués d'inhibiteurs d'ampk et d'agents de dégradation de protac et utilisations associées |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9004483D0 (en) * | 1990-02-28 | 1990-04-25 | Erba Carlo Spa | New aryl-and heteroarylethenylene derivatives and process for their preparation |
FR2678911A1 (fr) * | 1991-07-10 | 1993-01-15 | Prospection & Inventions | Cartouche tubulaire de stockage et d'application d'un produit non solide et ensemble d'entrainement et de poussee pour la cartouche. |
GB9115160D0 (en) * | 1991-07-12 | 1991-08-28 | Erba Carlo Spa | Methylen-oxindole derivatives and process for their preparation |
FR2694004B1 (fr) * | 1992-07-21 | 1994-08-26 | Adir | Nouvelles 3-(Hydroxybenzylidényl)-indoline-2-ones et 3-(hydroxybenzylidényl)-indoline-2-thiones, leurs procédés de préparation, et les compositions pharmaceutiques qui les contiennent. |
US5650415A (en) * | 1995-06-07 | 1997-07-22 | Sugen, Inc. | Quinoline compounds |
-
1999
- 1999-08-04 JP JP2000563824A patent/JP2002522452A/ja not_active Withdrawn
- 1999-08-04 AU AU54684/99A patent/AU5468499A/en not_active Abandoned
- 1999-08-04 WO PCT/US1999/017845 patent/WO2000008202A2/fr active Application Filing
- 1999-08-04 CA CA002383623A patent/CA2383623A1/fr not_active Abandoned
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8765748B2 (en) | 2007-12-21 | 2014-07-01 | University Health Network | Indazolyl, benzimidazolyl, benzotriazolyl substituted indolinone derivatives as kinase inhibitors useful in the treatment of cancer |
AU2008340991B2 (en) * | 2007-12-21 | 2012-02-23 | University Health Network | Indazolyl, benzimidazolyl, benzotriazolyl substituted indolinone derivatives as kinase inhibitors useful in the treatment of cancer |
WO2009079767A1 (fr) * | 2007-12-21 | 2009-07-02 | University Health Network | Dérivés d'indolmone à substitution indazolyle, benzimidazolyle, benzotriazolyle en tant qu'inhibiteurs de kinases utilisés dans le traitement du cancer |
WO2010115279A1 (fr) * | 2009-04-06 | 2010-10-14 | University Health Network | Inhibiteurs de kinases et procédé de traitement du cancer avec ceux-ci |
USRE47731E1 (en) | 2009-04-06 | 2019-11-19 | University Health Network | Kinase inhibitors and method of treating cancer with same |
US8999968B2 (en) | 2009-04-06 | 2015-04-07 | University Health Network | Kinase inhibitors and method of treating cancer with same |
US9139563B2 (en) | 2010-04-06 | 2015-09-22 | University Health Network | Kinase inhibitors and method of treating cancer |
US8481533B2 (en) | 2010-04-06 | 2013-07-09 | University Health Network | Kinase inhibitors and method of treating cancer |
US8263596B2 (en) | 2010-04-06 | 2012-09-11 | University Health Network | Kinase inhibitors and method of treating cancer |
US9579327B2 (en) | 2010-04-06 | 2017-02-28 | University Health Network | Synthesis of chiral 2-(1H-indazol-6-yl)-spiro[cyclopropane-1,3′-indolin]-2′-ones |
US9796703B2 (en) | 2010-04-06 | 2017-10-24 | University Health Network | Synthesis of chiral 2-(1H-indazol-6-yl)-spiro[cyclopropane-1,3′-indolin]-2′-ones |
US9907800B2 (en) | 2010-04-06 | 2018-03-06 | University Health Network | Kinase inhibitors and method of treating cancer |
US10077255B2 (en) | 2010-04-06 | 2018-09-18 | University Health Network | Synthesis of chiral 2-(1H-indazol-6-yl)-spiro[cyclopropane-1,3′-indolin]-2′-ones |
US10358436B2 (en) | 2010-04-06 | 2019-07-23 | University Health Network | Kinase inhibitors and method of treating cancer |
WO2012048411A1 (fr) * | 2010-10-13 | 2012-04-19 | University Health Network | Inhibiteurs de plk4 et méthode de traitement du cancer à l'aide de ceux-ci |
US20160250220A1 (en) | 2013-10-18 | 2016-09-01 | University Health Network | Treatment for pancreatic cancer |
US9642856B2 (en) | 2013-10-18 | 2017-05-09 | University Health Network | Treatment for pancreatic cancer |
Also Published As
Publication number | Publication date |
---|---|
WO2000008202A9 (fr) | 2000-07-27 |
WO2000008202A2 (fr) | 2000-02-17 |
AU5468499A (en) | 2000-02-28 |
JP2002522452A (ja) | 2002-07-23 |
WO2000008202A3 (fr) | 2000-05-18 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Dead |