JP2005508337A - 化合物 - Google Patents
化合物 Download PDFInfo
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- JP2005508337A JP2005508337A JP2003530699A JP2003530699A JP2005508337A JP 2005508337 A JP2005508337 A JP 2005508337A JP 2003530699 A JP2003530699 A JP 2003530699A JP 2003530699 A JP2003530699 A JP 2003530699A JP 2005508337 A JP2005508337 A JP 2005508337A
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- Prior art keywords
- compound
- physiologically functional
- disease
- alkyl
- compounds
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 125
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- -1 3-bromo-4-hydroxy-5- (2′methoxyphenyl) -benzylidene Chemical group 0.000 claims description 37
- 150000003839 salts Chemical class 0.000 claims description 34
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- 239000001257 hydrogen Substances 0.000 claims description 14
- 229910052736 halogen Chemical group 0.000 claims description 11
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- 241000124008 Mammalia Species 0.000 claims description 9
- 125000001246 bromo group Chemical group Br* 0.000 claims description 7
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- 239000003085 diluting agent Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
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- MQUFHXHELBTYIX-WQLSENKSSA-N (3z)-3-(1h-indol-3-ylmethylidene)-1h-pyrrolo[3,2-b]pyridin-2-one Chemical compound C1=CC=C2C(/C=C3/C4=NC=CC=C4NC3=O)=CNC2=C1 MQUFHXHELBTYIX-WQLSENKSSA-N 0.000 claims 1
- NXNQLECPAXXYTR-LCYFTJDESA-N (3z)-3-[(1-methylindol-3-yl)methylidene]-1h-pyrrolo[3,2-b]pyridin-2-one Chemical compound C12=CC=CC=C2N(C)C=C1\C=C/1C2=NC=CC=C2NC\1=O NXNQLECPAXXYTR-LCYFTJDESA-N 0.000 claims 1
- UAFSJUAEOZQXJJ-UHFFFAOYSA-N 3-(1h-indol-3-ylmethylidene)-1h-pyrrolo[2,3-b]pyridin-2-one Chemical compound C1=CC=C2C(C=C3C4=CC=CN=C4NC3=O)=CNC2=C1 UAFSJUAEOZQXJJ-UHFFFAOYSA-N 0.000 claims 1
- RJBBKRZRJMHITR-UHFFFAOYSA-N 3-[(1-methylindol-3-yl)methylidene]-1h-pyrrolo[2,3-b]pyridin-2-one Chemical compound C12=CC=CC=C2N(C)C=C1C=C1C2=CC=CN=C2NC1=O RJBBKRZRJMHITR-UHFFFAOYSA-N 0.000 claims 1
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- 125000003118 aryl group Chemical group 0.000 description 9
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- 125000001072 heteroaryl group Chemical group 0.000 description 6
- 125000000623 heterocyclic group Chemical group 0.000 description 6
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 5
- IHRRHTILSRVFPW-UHFFFAOYSA-N 1,3-dihydropyrrolo[3,2-b]pyridin-2-one Chemical group C1=CC=C2NC(=O)CC2=N1 IHRRHTILSRVFPW-UHFFFAOYSA-N 0.000 description 5
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Classifications
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- 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
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- A—HUMAN NECESSITIES
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- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
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- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- Immunology (AREA)
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- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32601201P | 2001-09-27 | 2001-09-27 | |
| PCT/US2002/030150 WO2003027111A1 (en) | 2001-09-27 | 2002-09-24 | Chemical compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005508337A true JP2005508337A (ja) | 2005-03-31 |
| JP2005508337A5 JP2005508337A5 (enExample) | 2005-12-22 |
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|---|---|---|---|
| JP2003530699A Pending JP2005508337A (ja) | 2001-09-27 | 2002-09-24 | 化合物 |
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| Country | Link |
|---|---|
| US (2) | US7015231B2 (enExample) |
| EP (1) | EP1430053B1 (enExample) |
| JP (1) | JP2005508337A (enExample) |
| AT (1) | ATE343575T1 (enExample) |
| DE (1) | DE60215682T2 (enExample) |
| ES (1) | ES2275021T3 (enExample) |
| WO (1) | WO2003027111A1 (enExample) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2001288374A1 (en) | 2000-09-01 | 2002-03-22 | Glaxo Group Limited | Substituted oxindole derivatives as tyrosine kinase inhibitors |
| US6964977B2 (en) | 2000-09-01 | 2005-11-15 | Smithkline Beecham Corporation | Oxindole derivatives |
| 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. |
| PL2383268T3 (pl) | 2005-02-04 | 2016-02-29 | Astrazeneca Ab | Pochodne pirazoliloaminopirydyny użyteczne jako inhibitory kinazy |
| PT1853588E (pt) | 2005-02-16 | 2008-08-25 | Astrazeneca Ab | Compostos químicos |
| WO2006087538A1 (en) * | 2005-02-16 | 2006-08-24 | Astrazeneca Ab | Chemical compounds |
| WO2007049041A1 (en) | 2005-10-28 | 2007-05-03 | Astrazeneca Ab | 4- (3-aminopyrazole) pyrimidine derivatives for use as tyrosine kinase inhibitors in the treatment of cancer |
| US7514435B2 (en) * | 2005-11-18 | 2009-04-07 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
| WO2007123269A1 (ja) | 2006-04-19 | 2007-11-01 | Astellas Pharma Inc. | アゾールカルボキサミド誘導体 |
| RU2461551C2 (ru) | 2007-10-24 | 2012-09-20 | Астеллас Фарма Инк. | Азолкарбоксамидное соединение или его фармацевтически приемлемая соль |
| US8426673B2 (en) | 2008-01-11 | 2013-04-23 | Astellas Pharma, Inc. | Pathological animal model for pelvic pain syndrome |
| CN106336400A (zh) | 2008-12-08 | 2017-01-18 | 萌蒂制药国际有限公司 | 酪氨酸激酶蛋白受体拮抗剂 |
| JP5778755B2 (ja) * | 2010-04-15 | 2015-09-16 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | ヒドロキノンの製造方法 |
| US8999992B2 (en) | 2013-03-15 | 2015-04-07 | Vm Pharma Llc | Crystalline forms of tryosine kinase inhibitors and their salts |
| CN103804273B (zh) * | 2014-01-27 | 2016-06-15 | 贵州大学 | 氧化吲哚与茚三酮双季碳拼接衍生物及其制备方法 |
| TWI672141B (zh) | 2014-02-20 | 2019-09-21 | 美商醫科泰生技 | 投予ｒｏｓ１突變癌細胞之分子 |
| US10301271B2 (en) | 2014-09-17 | 2019-05-28 | Purdue Pharma L.P. | Crystalline forms of tyrosine kinase inhibitors and their salts |
| KR102595599B1 (ko) | 2014-12-02 | 2023-11-02 | 이그니타, 인코포레이티드 | 신경모세포종의 치료를 위한 병용 |
| CN108697661A (zh) | 2015-12-18 | 2018-10-23 | 亚尼塔公司 | 用于治疗癌症的组合 |
| EP3654952A1 (en) | 2017-07-19 | 2020-05-27 | Ignyta, Inc. | Pharmaceutical compositions comprising entrectinib |
| JP7311498B2 (ja) | 2017-10-17 | 2023-07-19 | イグナイタ インコーポレイテッド | 薬学的組成物および剤形 |
| EP3942045A1 (en) | 2019-03-21 | 2022-01-26 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
| EP4054579A1 (en) | 2019-11-08 | 2022-09-14 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
Family Cites Families (5)
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| GB9423997D0 (en) * | 1994-11-28 | 1995-01-11 | Erba Carlo Spa | Substituted 3-arylidene-7-azaoxindole compounds and process for their preparation |
| GB9716557D0 (en) * | 1997-08-06 | 1997-10-08 | Glaxo Group Ltd | Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity |
| GB9721437D0 (en) * | 1997-10-10 | 1997-12-10 | Glaxo Group Ltd | Heteroaromatic compounds and their use in medicine |
| AU5468499A (en) | 1998-08-04 | 2000-02-28 | Sugen, Inc. | 3-methylidenyl-2-indolinone modulators of protein kinase |
| 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. |
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2002
- 2002-09-24 ES ES02799606T patent/ES2275021T3/es not_active Expired - Lifetime
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- 2002-09-24 EP EP02799606A patent/EP1430053B1/en not_active Expired - Lifetime
- 2002-09-24 US US10/490,831 patent/US7015231B2/en not_active Expired - Fee Related
- 2002-09-24 JP JP2003530699A patent/JP2005508337A/ja active Pending
- 2002-09-24 AT AT02799606T patent/ATE343575T1/de not_active IP Right Cessation
- 2002-09-24 WO PCT/US2002/030150 patent/WO2003027111A1/en not_active Ceased
-
2006
- 2006-01-20 US US11/336,010 patent/US20060128745A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| WO2003027111A1 (en) | 2003-04-03 |
| EP1430053B1 (en) | 2006-10-25 |
| ES2275021T3 (es) | 2007-06-01 |
| ATE343575T1 (de) | 2006-11-15 |
| US7015231B2 (en) | 2006-03-21 |
| DE60215682D1 (de) | 2006-12-07 |
| DE60215682T2 (de) | 2007-09-06 |
| EP1430053A1 (en) | 2004-06-23 |
| US20040198766A1 (en) | 2004-10-07 |
| US20060128745A1 (en) | 2006-06-15 |
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