MY127956A - Substituted indolines which inhibit receptor tyrosine kinases - Google Patents
Substituted indolines which inhibit receptor tyrosine kinasesInfo
- Publication number
- MY127956A MY127956A MYPI20004762A MYPI20004762A MY127956A MY 127956 A MY127956 A MY 127956A MY PI20004762 A MYPI20004762 A MY PI20004762A MY PI20004762 A MYPI20004762 A MY PI20004762A MY 127956 A MY127956 A MY 127956A
- Authority
- MY
- Malaysia
- Prior art keywords
- receptor tyrosine
- tyrosine kinases
- inhibit receptor
- substituted indolines
- substituted
- 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
- C07D403/02—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
- C07D403/12—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 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
-
- 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
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- 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
-
- 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
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Ophthalmology & Optometry (AREA)
- Rheumatology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Transplantation (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
THE INVENTION RELATES TO INDOLINONES OF GENERAL FORMULA SUBSTITUTED IN THE 6 POSITION, WHEREIN R1 TO R5 AND X ARE DEFINED AS IN CLAIM 1, THE ISOMERS AND THE SALTS THEREOF, PARTICULARLY THE PHYSIOLOGICALLY ACCEPTABLE SALTS THEREOF WHICH HAVE VALUEABLE PHARMACOLOGICAL PROPERTIES, ESPECIALLY AN INHIBITORY EFFECT ON RECEPTOR TYROSINE KINASES AND CYCLIN/CDK COMPLEXES, AS WELL AS ON THE PROLIFERATION OF ENDOTHELIAL CELLS AND VARIOUS TUMOUR CELLS, PHARMACEUTICAL COMPOSITIONS CONTAINING THESE COMPOUNDS, THEIR USE AND PROCESSES FOR PREPARING THEM.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19949208A DE19949208A1 (en) | 1999-10-13 | 1999-10-13 | New 3-(amino-methylene)-2-indolinone derivatives are kinase inhibitors and cell proliferation inhibitors useful e.g. for treating tumors, metastasis, rheumatoid arthritis or psoriasis |
| DE2000142696 DE10042696A1 (en) | 2000-08-31 | 2000-08-31 | New 3-(amino-methylene)-2-indolinone derivatives are kinase inhibitors and cell proliferation inhibitors useful e.g. for treating tumors, metastasis, rheumatoid arthritis or psoriasis |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MY127956A true MY127956A (en) | 2007-01-31 |
Family
ID=26006858
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MYPI20004762A MY127956A (en) | 1999-10-13 | 2000-10-11 | Substituted indolines which inhibit receptor tyrosine kinases |
Country Status (43)
Families Citing this family (108)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19816624A1 (en) * | 1998-04-15 | 1999-10-21 | Boehringer Ingelheim Pharma | Novel substituted indolinones, their preparation and their use as pharmaceuticals |
| EP1415987B1 (en) | 2000-10-20 | 2007-02-28 | Eisai R&D Management Co., Ltd. | Nitrogenous aromatic ring compounds as anti cancer agents |
| US6638965B2 (en) | 2000-11-01 | 2003-10-28 | Boehringer Ingelheim Pharma Kg | Substituted indolinones, preparation thereof and their use as pharmaceutical compositions |
| DE10117204A1 (en) | 2001-04-06 | 2002-10-10 | Boehringer Ingelheim Pharma | Indolinones substituted in the 6-position, their preparation and their use as medicaments |
| US7700610B2 (en) | 2001-06-29 | 2010-04-20 | Ab Science | Use of tyrosine kinase inhibitors for treating allergic diseases |
| EP1471907B1 (en) * | 2001-06-29 | 2008-07-16 | AB Science | Use of c-kit inhibitors for treating autoimmune diseases |
| PT1401416E (en) | 2001-06-29 | 2007-02-28 | Ab Science | Use of c-kit inhibitors for treating inflammatory bowel diseases (ibd) |
| CA2452169A1 (en) | 2001-06-29 | 2003-01-09 | Ab Science | Use of tyrosine kinase inhibitors for treating inflammatory diseases |
| EP1434991B1 (en) * | 2001-06-29 | 2007-10-17 | AB Science | New potent, selective and non toxic c-kit inhibitors |
| US20030091974A1 (en) * | 2001-06-29 | 2003-05-15 | Alain Moussy | Method for screening compounds capable of depleting mast cells |
| US20030225152A1 (en) * | 2001-09-27 | 2003-12-04 | Andrews Steven W. | 3-(Arylamino)methylene-1, 3-dihydro-2h-indol-2-ones as kinase inhibitors |
| US6797825B2 (en) | 2001-12-13 | 2004-09-28 | Abbott Laboratories | Protein kinase inhibitors |
| US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
| WO2003057690A1 (en) | 2001-12-27 | 2003-07-17 | Theravance, Inc. | Indolinone derivatives useful as protein kinase inhibitors |
| SE0302546D0 (en) | 2003-09-24 | 2003-09-24 | Astrazeneca Ab | New compounds |
| ITBO20020198A1 (en) * | 2002-04-12 | 2003-10-13 | Univ Bologna | DERIVATIVES 2, 5 BIS DIAMMINO 1, 4 BENZOCHENIONIC USEFUL FOR THE TREATMENT OF ALZHEIMER DISEASE, METHOD FOR THEIR PREPARATION AND |
| US7514468B2 (en) | 2002-07-23 | 2009-04-07 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Indolinone derivatives substituted in the 6 position, the preparation thereof and their use as pharmaceutical compositions |
| US7169936B2 (en) | 2002-07-23 | 2007-01-30 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Indolinone derivatives substituted in the 6-position, their preparation and their use as medicaments |
| DE10233500A1 (en) | 2002-07-24 | 2004-02-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 3-Z- [1- (4- (N - ((4-methyl-piperazin-1-yl) -methylcarbonyl) -N-methyl-amino) -anilino) -1-phenyl-methylene] -6-methoxycarbonyl- 2-indolinone monoethanesulfonate and its use as a medicament |
| US20040204458A1 (en) | 2002-08-16 | 2004-10-14 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Use of Lck inhibitors for treatment of immunologic diseases |
| DE10237423A1 (en) * | 2002-08-16 | 2004-02-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Treating immunological (or related) diseases, e.g. inflammatory bowel disease, rheumatoid arthritis or psoriasis, comprises administration of 3-methylene-2-indolinone derivative or quinazoline compound |
| US7148249B2 (en) | 2002-09-12 | 2006-12-12 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Indolinones substituted by heterocycles, the preparation thereof and their use as medicaments |
| JP4879492B2 (en) * | 2002-11-27 | 2012-02-22 | アラーガン、インコーポレイテッド | Kinase inhibitors for the treatment of diseases |
| 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 |
| WO2005044788A1 (en) | 2003-11-11 | 2005-05-19 | Eisai Co., Ltd. | Urea derivative and process for producing the same |
| SE0401790D0 (en) * | 2004-07-07 | 2004-07-07 | Forskarpatent I Syd Ab | Tamoxifen response in pre- and postmenopausal breast cancer patients |
| US20060058311A1 (en) * | 2004-08-14 | 2006-03-16 | Boehringer Ingelheim International Gmbh | Combinations for the treatment of diseases involving cell proliferation |
| US8772269B2 (en) | 2004-09-13 | 2014-07-08 | Eisai R&D Management Co., Ltd. | Use of sulfonamide-including compounds in combination with angiogenesis inhibitors |
| EP1797877A4 (en) | 2004-09-13 | 2010-12-15 | Eisai Co Ltd | Joint use of sulfonamide based compound with angiogenesis inhibitor |
| ATE428421T1 (en) | 2004-09-17 | 2009-05-15 | Eisai R&D Man Co Ltd | MEDICAL COMPOSITION WITH IMPROVED STABILITY AND REDUCED GELING PROPERTIES |
| PE20060777A1 (en) * | 2004-12-24 | 2006-10-06 | Boehringer Ingelheim Int | INDOLINONE DERIVATIVES FOR THE TREATMENT OR PREVENTION OF FIBROTIC DISEASES |
| EP1925676A4 (en) | 2005-08-02 | 2010-11-10 | Eisai R&D Man Co Ltd | METHOD FOR ANALYZING THE EFFECT OF A VASCULARIZATION INHIBITOR |
| WO2007057397A1 (en) * | 2005-11-15 | 2007-05-24 | Boehringer Ingelheim International Gmbh | Treatment of cancer |
| WO2007136103A1 (en) | 2006-05-18 | 2007-11-29 | Eisai R & D Management Co., Ltd. | Antitumor agent for thyroid cancer |
| EP1870400A1 (en) * | 2006-06-08 | 2007-12-26 | Boehringer Ingelheim Pharma GmbH & Co. KG | Salts and crystalline salt forms of an 2-indolinone derivative |
| KR101472600B1 (en) | 2006-08-28 | 2014-12-15 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | Antitumor agent for undifferentiated gastric cancer |
| EP2119707B1 (en) | 2007-01-29 | 2015-01-14 | Eisai R&D Management Co., Ltd. | Composition for treatment of undifferentiated-type of gastric cancer |
| US20100184747A1 (en) * | 2007-06-12 | 2010-07-22 | Boehringer Ingelheim International Gmbh | Indoline derivatives and their use in treating disease-states such as cancer |
| DK2170827T3 (en) | 2007-06-21 | 2013-11-18 | Janssen Pharmaceutica Nv | Indoline-2-ones and aza-indoline-2-ones |
| CN101848895B (en) | 2007-11-09 | 2013-10-23 | 卫材R&D管理有限公司 | Combined use of angiogenesis inhibitory substance and antitumor platinum complex |
| WO2009071523A1 (en) | 2007-12-03 | 2009-06-11 | Boehringer Ingelheim International Gmbh | Process for the manufacture of an indolinone derivative |
| PE20091445A1 (en) * | 2007-12-03 | 2009-10-19 | Boehringer Ingelheim Int | INDOLINONE DERIVATIVES AND PROCEDURE FOR ITS MANUFACTURE |
| MY158929A (en) | 2008-06-06 | 2016-11-30 | Boehringer Ingelheim Int | Pharmaceutical combination |
| JP5651110B2 (en) | 2008-07-29 | 2015-01-07 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | New compounds |
| WO2010081817A1 (en) | 2009-01-14 | 2010-07-22 | Boehringer Ingelheim International Gmbh | Method for treating colorectal cancer |
| US8802384B2 (en) | 2009-03-12 | 2014-08-12 | Boehringer Ingelheim International Gmbh | Method or system using biomarkers for the monitoring of a treatment |
| WO2010108503A1 (en) | 2009-03-24 | 2010-09-30 | Life & Brain Gmbh | Promotion of neuronal integration in neural stem cell grafts |
| EP2647375A1 (en) | 2009-05-14 | 2013-10-09 | Boehringer Ingelheim International Gmbh | Combination of vargatef and dabigatran for the treatment of oncological and fibrotic diseases |
| BR112012003592B8 (en) | 2009-08-19 | 2021-05-25 | Eisai R&D Man Co Ltd | pharmaceutical composition containing quinoline derivative |
| US20120107304A1 (en) | 2010-04-27 | 2012-05-03 | Boehringer Ingelheim International Gmbh | Combination therapy in treatment of oncological and fibrotic diseases |
| CA2802644C (en) | 2010-06-25 | 2017-02-21 | Eisai R & D Management Co., Ltd. | Antitumor agent using compounds having kinase inhibitory effect in combination |
| WO2012068441A2 (en) | 2010-11-19 | 2012-05-24 | Ratiopharm Gmbh | Intedanib salts and solid state forms thereof |
| EP2700403B1 (en) | 2011-04-18 | 2015-11-25 | Eisai R&D Management Co., Ltd. | Therapeutic agent for tumor |
| WO2012166899A2 (en) | 2011-06-03 | 2012-12-06 | Eisai R&D Management Co., Ltd. | Biomarkers for predicting and assessing responsiveness of thyroid and kidney cancer subjects to lenvatinib compounds |
| WO2013059740A1 (en) | 2011-10-21 | 2013-04-25 | Foundation Medicine, Inc. | Novel alk and ntrk1 fusion molecules and uses thereof |
| EP3604307A1 (en) | 2012-01-26 | 2020-02-05 | Angion Biomedica Corp. | Anti-fibrotic compounds and uses thereof |
| WO2014071419A2 (en) | 2012-11-05 | 2014-05-08 | Foundation Medicine, Inc. | Novel fusion molecules and uses thereof |
| AU2013337277B2 (en) | 2012-11-05 | 2018-03-08 | Foundation Medicine, Inc. | Novel NTRK1 fusion molecules and uses thereof |
| US9642851B2 (en) | 2012-12-06 | 2017-05-09 | Kbp Biosciences Co., Ltd. | Indolinone derivative as tyrosine kinase inhibitor |
| AU2013364953A1 (en) | 2012-12-21 | 2015-04-30 | Eisai R&D Management Co., Ltd. | Amorphous form of quinoline derivative, and method for producing same |
| WO2014113729A2 (en) | 2013-01-18 | 2014-07-24 | Foundation Mecicine, Inc. | Methods of treating cholangiocarcinoma |
| US20140350022A1 (en) | 2013-05-10 | 2014-11-27 | Boehringer Ingelheim International Gmbh | Efficacious treatment of NSCLC and predictive clinical marker of the responsiveness of a tumour to a treatment |
| CN105264380B (en) | 2013-05-14 | 2017-09-05 | 卫材R&D管理有限公司 | Biomarkers for predicting and evaluating responsiveness of endometrial cancer subjects to lenvatinib compounds |
| CN104003925B (en) * | 2013-06-05 | 2016-03-30 | 四川大学 | Indolinone compound or its derivative and use thereof |
| WO2015009889A1 (en) * | 2013-07-18 | 2015-01-22 | Concert Pharmaceuticals, Inc. | Deuterated intedanib derivatives and their use for the treatment of proliferative disorders |
| JP6799201B2 (en) | 2013-07-31 | 2020-12-16 | アヴァリン ファーマ インク. | Aerosol Tyrosine Kinase Inhibitor Compounds and Their Use |
| CA2957005C (en) | 2014-08-28 | 2021-10-12 | Eisai R&D Management Co., Ltd. | High-purity quinoline derivative and method for manufacturing same |
| CN104262232B (en) * | 2014-09-09 | 2016-05-04 | 苏州明锐医药科技有限公司 | The preparation method of Ni Taidani |
| SG11201706630UA (en) | 2015-02-25 | 2017-09-28 | Eisai R&D Man Co Ltd | Method for suppressing bitterness of quinoline derivative |
| WO2016140717A1 (en) | 2015-03-04 | 2016-09-09 | Merck Sharp & Dohme Corp. | Combination of a pd-1 antagonist and a vegfr/fgfr/ret tyrosine kinase inhibitor for treating cancer |
| WO2016178064A1 (en) | 2015-05-06 | 2016-11-10 | Suven Life Sciences Limited | Polymorph of nintedanib ethanesulphonate, processes and intermediates thereof |
| CN104844499B (en) * | 2015-06-05 | 2017-03-08 | 北京康立生医药技术开发有限公司 | One kettle way prepares the synthetic method of Nintedanib |
| ES2971096T3 (en) * | 2015-06-06 | 2024-06-03 | Cloudbreak Therapeutics Llc | Compositions and methods for treating therygium |
| BR112017027227B1 (en) | 2015-06-16 | 2023-12-12 | Eisai R&D Management Co., Ltd | ANTI-CANCER AGENT |
| CN105126909B (en) * | 2015-07-13 | 2018-01-23 | 淮海工学院 | Application of the immobilized palladium catalyst in the synthesis of the nitrobenzene methyl of 4 phenylacetylene base 3 |
| CZ308695B6 (en) | 2015-07-29 | 2021-03-03 | Zentiva, K.S. | Process for preparing methyl (Z) -3 - [[4- [methyl [2- (4-methyl-1-piperazinyl) acetyl] amino] phenyl] amino] phenylmethylene) -oxindole-6-carboxylate (intedanib, nintedanib) |
| CN106467500A (en) * | 2015-08-14 | 2017-03-01 | 廊坊百瑞化工有限公司 | A kind of one pot synthesis synthesize the new method of Nintedanib key intermediate |
| JP6553726B2 (en) | 2015-08-20 | 2019-07-31 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Tumor therapeutic agent |
| MY195904A (en) | 2015-12-24 | 2023-02-27 | Respivert Ltd | Indolinones Compounds and Their use in the Treatment Of Fibrotic Diseases |
| CZ2016104A3 (en) | 2016-02-24 | 2017-09-06 | Zentiva, K.S. | Crystalline modifications of methyl (3Z)-3- {[(4-{methyl[(4-methylpiperazin-1yl)acetyl]amino}phenyl)amino](phenyl)methylidene}-2oxo-2,3-dihydro-1H-indole-6-carboxylate and the methods of their preparation |
| JP7039480B2 (en) | 2016-03-08 | 2022-03-22 | レスピバート・リミテツド | Indole derivatives and their use as protein kinase inhibitors |
| WO2017178428A1 (en) | 2016-04-13 | 2017-10-19 | Boehringer Ingelheim International Gmbh | Pharmaceutical combination of nintedanib, trifluridine and tipiracil for treating colorectal cancer |
| EP3246029A1 (en) | 2016-05-19 | 2017-11-22 | Boehringer Ingelheim International Gmbh | Pharmaceutical combination of nintedanib and capecitabine for the treatment of colorectal cancer |
| WO2017203027A1 (en) | 2016-05-27 | 2017-11-30 | Boehringer Ingelheim International Gmbh | Use of ecm biomarkers for the determining the treatment onset with nintedanib and pirfenidone |
| WO2017207643A1 (en) | 2016-06-01 | 2017-12-07 | Boehringer Ingelheim International Gmbh | Use of ecm biomarkers for the determining the treatment onset with nintedanib and pirfenidone |
| CA3026118A1 (en) | 2016-06-02 | 2017-12-07 | Cloudbreak Therapeutics, Llc | Compositions and methods of using nintedanib for treating ocular diseases with abnormal neovascularization |
| US10159660B2 (en) | 2016-07-29 | 2018-12-25 | Oncternal Therapeutics, Inc. | Uses of indolinone compounds |
| CN106748960A (en) * | 2016-11-30 | 2017-05-31 | 瑞阳制药有限公司 | The potential impurity compound of Nintedanib, preparation method, using and its detection method |
| CN106748961A (en) * | 2016-11-30 | 2017-05-31 | 瑞阳制药有限公司 | The impurity compound of Nintedanib, preparation method, using and its detection method |
| JP2019536812A (en) | 2016-12-12 | 2019-12-19 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Nintedanib for use in methods of treating interstitial lung disease by co-administration with olodaterol |
| US12303505B2 (en) | 2017-02-08 | 2025-05-20 | Eisai R&D Management Co., Ltd. | Tumor-treating pharmaceutical composition |
| WO2018177893A1 (en) | 2017-03-28 | 2018-10-04 | Boehringer Ingelheim International Gmbh | Nintedanib for use in methods for the treatment of muscular dystrophy |
| BR112019023064A2 (en) | 2017-05-16 | 2020-06-09 | Eisai R&D Man Co Ltd | treatment of hepatocellular carcinoma |
| HRP20251042T1 (en) | 2017-10-23 | 2025-10-24 | Boehringer Ingelheim International Gmbh | New combination of active agents for the treatment of progressive fibrosing interstitial lung diseases (pf-ild) |
| JP7382317B2 (en) | 2017-11-17 | 2023-11-16 | フェルミオン オサケ ユキチュア | Synthesis of 2-indolinone derivatives known as intermediates for producing nintedanib |
| JP7061310B2 (en) * | 2018-04-05 | 2022-04-28 | 国立大学法人 大分大学 | Pharmaceuticals for the prevention and treatment of chronic fatty diseases |
| CN108358827A (en) * | 2018-05-07 | 2018-08-03 | 日照市普达医药科技有限公司 | It is a kind of to treat psoriasic 2- oxo-indoles analog derivative and preparation method thereof |
| CN112165934A (en) | 2018-05-25 | 2021-01-01 | 克劳德布雷克医疗有限责任公司 | Compositions and methods for treating ocular congestion |
| SG11202103459WA (en) * | 2018-10-05 | 2021-05-28 | Ichnos Sciences S A | Indolinone compounds for use as map4k1 inhibitors |
| JP2023519600A (en) | 2020-04-01 | 2023-05-11 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Use of biomarkers in treating fibrotic conditions |
| CN111848490B (en) * | 2020-08-24 | 2021-09-24 | 江西国药有限责任公司 | A kind of preparation method of high-purity nintedanib ethanesulfonate |
| CN112574094B (en) * | 2020-12-14 | 2022-07-01 | 成都大学 | Indolone derivatives and pharmaceutical use thereof |
| US20240238368A1 (en) | 2021-01-25 | 2024-07-18 | Nibec Co., Ltd. | Peptide for preventing and treating fibrosis |
| EP4098246A1 (en) | 2021-05-31 | 2022-12-07 | Lotus Pharmaceutical Co., Ltd. | Formulation of nintedanib |
| CN115703758B (en) * | 2021-08-12 | 2024-03-26 | 中国医学科学院药物研究所 | Compounds used as kinase inhibitors, preparation method and application thereof |
| WO2024037982A1 (en) | 2022-08-16 | 2024-02-22 | Boehringer Ingelheim International Gmbh | Pharmaceutical formulations of nintedanib for intraocular use |
| TWI857798B (en) * | 2023-09-28 | 2024-10-01 | 國立臺灣大學 | Indoline derivatives for treatment and/or prevention of tumor or cell proliferative and fibrosis diseases |
| CN121226225A (en) * | 2025-08-26 | 2025-12-30 | 沈阳兴齐眼药股份有限公司 | Ureidindolone compounds, their preparation methods and uses |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE558210A (en) * | 1956-06-08 | |||
| CA2166722A1 (en) * | 1994-05-06 | 1995-11-16 | Manoj L. Maniar | Use of vitamin e tocopheryl derivatives in ophthalmic compositions |
| US5880141A (en) * | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
| HUP9800757A3 (en) * | 1996-01-17 | 1998-08-28 | Taiho Pharmaceutical Co Ltd | Intimal thickening inhibitors containing oxyindole derivatives and pharmaceutical compositions containing them |
| GB9718913D0 (en) * | 1997-09-05 | 1997-11-12 | Glaxo Group Ltd | Substituted oxindole derivatives |
| DE19815020A1 (en) * | 1998-04-03 | 1999-10-07 | Boehringer Ingelheim Pharma | New substituted indolinones, their production and their use as medicines |
| DE19816624A1 (en) * | 1998-04-15 | 1999-10-21 | Boehringer Ingelheim Pharma | Novel substituted indolinones, their preparation and their use as pharmaceuticals |
| DE19824922A1 (en) * | 1998-06-04 | 1999-12-09 | Boehringer Ingelheim Pharma | Novel substituted indolinones, their preparation and their use as pharmaceuticals |
| GB9904933D0 (en) * | 1999-03-04 | 1999-04-28 | Glaxo Group Ltd | Compounds |
-
2000
- 2000-09-10 UA UA2002053890A patent/UA75054C2/en unknown
- 2000-10-09 JP JP2001530102A patent/JP4021664B2/en not_active Expired - Lifetime
- 2000-10-09 ME MEP-454/08A patent/MEP45408A/en unknown
- 2000-10-09 WO PCT/EP2000/009867 patent/WO2001027081A1/en not_active Ceased
- 2000-10-09 MX MXPA02002799A patent/MXPA02002799A/en active IP Right Grant
- 2000-10-09 SI SI200031039T patent/SI1224170T1/en unknown
- 2000-10-09 AU AU10233/01A patent/AU781939B2/en not_active Expired
- 2000-10-09 RS YUP-266/02A patent/RS51013B/en unknown
- 2000-10-09 EP EP09164507A patent/EP2157081A1/en not_active Withdrawn
- 2000-10-09 CZ CZ20021410A patent/CZ301073B6/en not_active IP Right Cessation
- 2000-10-09 EP EP00971347.0A patent/EP1224170B9/en not_active Expired - Lifetime
- 2000-10-09 ES ES00971347T patent/ES2331459T3/en not_active Expired - Lifetime
- 2000-10-09 DK DK00971347.0T patent/DK1224170T5/en active
- 2000-10-09 KR KR1020077017807A patent/KR100857734B1/en not_active Expired - Lifetime
- 2000-10-09 BR BRPI0014735-4 patent/BRPI0014735B8/en active IP Right Grant
- 2000-10-09 SK SK646-2002A patent/SK287312B6/en not_active IP Right Cessation
- 2000-10-09 HU HU0204587A patent/HU230416B1/en active Protection Beyond IP Right Term
- 2000-10-09 NZ NZ518489A patent/NZ518489A/en not_active IP Right Cessation
- 2000-10-09 PT PT00971347T patent/PT1224170E/en unknown
- 2000-10-09 HR HR20020306A patent/HRP20020306B1/en not_active IP Right Cessation
- 2000-10-09 DE DE50015711T patent/DE50015711D1/en not_active Expired - Lifetime
- 2000-10-09 EA EA200200380A patent/EA006080B1/en not_active IP Right Cessation
- 2000-10-09 CN CNB008158681A patent/CN100455568C/en not_active Expired - Lifetime
- 2000-10-09 KR KR1020027004701A patent/KR100835546B1/en not_active Expired - Lifetime
- 2000-10-09 HK HK03104649.4A patent/HK1052505B/en not_active IP Right Cessation
- 2000-10-09 IL IL14875600A patent/IL148756A0/en active IP Right Grant
- 2000-10-09 CA CA002387013A patent/CA2387013C/en not_active Expired - Lifetime
- 2000-10-09 PL PL355433A patent/PL207445B1/en not_active IP Right Cessation
- 2000-10-09 EE EEP200200197A patent/EE05427B1/en active Protection Beyond IP Right Term
- 2000-10-09 AT AT00971347T patent/ATE439342T1/en active
- 2000-10-11 EG EG2000101293A patent/EG25931A/en active
- 2000-10-11 PE PE2000001088A patent/PE20010671A1/en not_active IP Right Cessation
- 2000-10-11 MY MYPI20004762A patent/MY127956A/en unknown
- 2000-10-12 CO CO00077925A patent/CO5261488A1/en not_active Application Discontinuation
- 2000-10-12 TW TW089121320A patent/TWI268922B/en not_active IP Right Cessation
- 2000-10-13 AR ARP000105394A patent/AR026036A1/en active IP Right Grant
-
2001
- 2001-02-06 SA SA01210704A patent/SA01210704B1/en unknown
-
2002
- 2002-03-19 IL IL148756A patent/IL148756A/en active Protection Beyond IP Right Term
- 2002-04-05 BG BG106587A patent/BG65983B1/en unknown
- 2002-04-11 NO NO20021719A patent/NO322746B1/en active Protection Beyond IP Right Term
-
2007
- 2007-08-15 JP JP2007211755A patent/JP2007302697A/en active Pending
-
2009
- 2009-11-06 CY CY20091101152T patent/CY1110067T1/en unknown
-
2015
- 2015-03-13 CY CY2015009C patent/CY2015009PI2/en unknown
- 2015-03-16 LT LTPA2015015C patent/LTC1224170I2/en unknown
- 2015-03-16 NL NL300725C patent/NL300725I2/en unknown
- 2015-03-16 FR FR15C0024C patent/FR15C0024I2/en active Active
- 2015-03-16 LU LU92681C patent/LU92681I2/en unknown
- 2015-03-16 BE BE2015C018C patent/BE2015C018I2/fr unknown
- 2015-03-18 NO NO2015009C patent/NO2015009I1/en unknown
-
2016
- 2016-05-13 HU HUS1600022C patent/HUS1600022I1/en unknown
-
2023
- 2023-09-05 NO NO2023033C patent/NO2023033I1/en unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MY122357A (en) | Indolinones having kinase inhibitory activity | |
| BG104938A (en) | SUBSTITUTED INDONALINES, THEIR RECEIVING AND THEIR USE AS MEDICINAL PRODUCTS | |
| MEP45408A (en) | 6-position substituted indoline, production and use thereof as a medicament | |
| NO20011477L (en) | Novel substituted indolinones with inhibitory effect on various kinases and cyclin / CDK complexes | |
| WO1999057117A3 (en) | Indole derivatives and their use in the treatment of malignant and other diseases caused by pathological cell proliferation | |
| YU61402A (en) | Pyrrole substituted 2-indolinone protein kinase inhibitors | |
| MY156407A (en) | 5-phenylthiazole derivatives and use as p13 kinase inhibitors | |
| TNSN03055A1 (en) | 3-(4-amidopyrrol -2-ylmethlidene)-2- indolinone derivatives as protein kinase inhibitors | |
| MX2010003927A (en) | Pyrrolo [2, 3 -d] pyrimidin derivatives as protein kinase b inhibitors. | |
| CY1106933T1 (en) | Pyrimidine compounds | |
| MXPA04006271A (en) | Indolinone derivatives useful as protein kinase inhibitors. | |
| PL344004A1 (en) | Pyrazole derivatives as p-38 map kinase inhibitors | |
| PL1608647T3 (en) | 5-phenylthiazole derivatives and their use as p13 kinase inhibitors | |
| WO2004026829A3 (en) | Heterocyclically substituted indolinones and their use as receptor tyrosine kinase inhibitors | |
| WO2001027080A3 (en) | 5-substituted indolinones and use thereof as kinase and cyclin/cdk complex inhibitors | |
| AU3864500A (en) | Substituted aza-oxindole derivatives | |
| MX2007011695A (en) | Substituted oxindole derivatives, medicaments containing the latter and use thereof. | |
| MY138141A (en) | Indolinone derivatives, substituted in the 6-position, their preparation and their use as medicaments | |
| BR0208900A (en) | Position 6 substituted indolines and their use as kinase inhibitors | |
| BG106044A (en) | Substituted 1,4-dihydroindeno[1,2-c]pyrazoles as inhibitors of tyrosine kinase | |
| BRPI0416994A (en) | Advanced indolinone-based protein kinase inhibitors | |
| UY26308A1 (en) | NEW SUBSTITUTED INDOLINONES, THEIR PREPARATION AND THEIR USE AS MEDICINES | |
| TH55950B (en) | Indo-Linone displaced in position-6, the preparation of these compounds And the use of these substances as pharmaceutical components | |
| UY26390A1 (en) | SUBSTITUTED INDOLINONES IN POSITION 5, THEIR PREPARATION AND THEIR USE AS MEDICINES | |
| UY27968A1 (en) | DERIVATIVES OF INDOLINONA REPLACED WITH HETEROCICLES, ITS PREPARATION AND ITS USE AS MEDICATIONS. |