CN101848908B - 激酶抑制剂的组合物及其在治疗癌症和其它与激酶相关的疾病中的用途 - Google Patents
激酶抑制剂的组合物及其在治疗癌症和其它与激酶相关的疾病中的用途 Download PDFInfo
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- CN101848908B CN101848908B CN200880114705.9A CN200880114705A CN101848908B CN 101848908 B CN101848908 B CN 101848908B CN 200880114705 A CN200880114705 A CN 200880114705A CN 101848908 B CN101848908 B CN 101848908B
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- 0 *c1c(-c(c(*)c2*)c(*)c(C3)c2N(*)C3=O)nc(*)[s]1 Chemical compound *c1c(-c(c(*)c2*)c(*)c(C3)c2N(*)C3=O)nc(*)[s]1 0.000 description 4
- UUJHVQXUVWFTCG-UHFFFAOYSA-N CCNCCNC(C=C(C)C)O Chemical compound CCNCCNC(C=C(C)C)O UUJHVQXUVWFTCG-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
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- 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
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- 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
- C07D417/02—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 two hetero rings
- C07D417/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Communicable Diseases (AREA)
- Vascular Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Obesity (AREA)
- Hospice & Palliative Care (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Psychiatry (AREA)
- Gastroenterology & Hepatology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US97041007P | 2007-09-06 | 2007-09-06 | |
| US60/970,410 | 2007-09-06 | ||
| US1338907P | 2007-12-13 | 2007-12-13 | |
| US61/013,389 | 2007-12-13 | ||
| US7429508P | 2008-06-20 | 2008-06-20 | |
| US61/074,295 | 2008-06-20 | ||
| PCT/US2008/075418 WO2009033033A2 (en) | 2007-09-06 | 2008-09-05 | Compositions of kinase inhibitors and their use for treatment of cancer and other diseases related to kinases |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101848908A CN101848908A (zh) | 2010-09-29 |
| CN101848908B true CN101848908B (zh) | 2014-07-02 |
Family
ID=40429714
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200880114705.9A Active CN101848908B (zh) | 2007-09-06 | 2008-09-05 | 激酶抑制剂的组合物及其在治疗癌症和其它与激酶相关的疾病中的用途 |
Country Status (15)
| Country | Link |
|---|---|
| US (5) | US8299106B2 (https=) |
| EP (2) | EP3037419B1 (https=) |
| JP (5) | JP5452490B2 (https=) |
| CN (1) | CN101848908B (https=) |
| CA (1) | CA2736177A1 (https=) |
| CY (1) | CY1118012T1 (https=) |
| DK (1) | DK2197878T3 (https=) |
| ES (2) | ES2759347T3 (https=) |
| HR (1) | HRP20161114T1 (https=) |
| HU (1) | HUE030774T2 (https=) |
| LT (1) | LT2197878T (https=) |
| PL (1) | PL2197878T3 (https=) |
| PT (1) | PT2197878T (https=) |
| SI (1) | SI2197878T1 (https=) |
| WO (1) | WO2009033033A2 (https=) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3037419B1 (en) * | 2007-09-06 | 2019-09-04 | Boston Biomedical, Inc. | Compositions of kinase inhibitors and their use for treatment of cancer and other diseases related to kinases |
| KR101300916B1 (ko) * | 2007-12-10 | 2013-08-27 | 인터디지탈 패튼 홀딩스, 인크 | 무선 링크 제어 패킷 폐기 및 무선 링크 제어 재확립을 트리거하는 방법 및 장치 |
| US20130331381A1 (en) | 2011-02-28 | 2013-12-12 | Mcmaster University | Treatment of Cancer WIth Dopamine Receptor Antagonists |
| EP2888254B1 (en) | 2012-08-23 | 2016-10-05 | The Institute of Cancer Research: Royal Cancer Hospital | Fused heterocyclic compounds and their use |
| US9187454B2 (en) | 2013-03-13 | 2015-11-17 | Boston Biomedical, Inc. | Inhibitors of kinases and cancer stem cells, and methods of preparation and use thereof |
| US9227962B2 (en) | 2013-03-13 | 2016-01-05 | Boston Biomedical, Inc. | Heterocyclic substituted-3-heteroarylidenyl-2-indolinone derivative |
| HK1220184A1 (zh) * | 2013-03-13 | 2017-04-28 | Boston Biomedical, Inc. | 用於治疗癌症的作为癌症干细胞途径激酶抑制剂的3-(芳基或杂芳基)甲基吲哚-2-酮衍生物 |
| WO2014202528A1 (en) * | 2013-06-20 | 2014-12-24 | Boehringer Ingelheim International Gmbh | Olefin substituted oxindoles having ampk activity |
| RU2016128396A (ru) * | 2014-01-27 | 2018-03-02 | Бостон Биомедикал, Инк. | Новые способы лечения рака |
| US10118890B2 (en) | 2014-10-10 | 2018-11-06 | The Research Foundation For The State University Of New York | Trifluoromethoxylation of arenes via intramolecular trifluoromethoxy group migration |
| CN107683137A (zh) * | 2015-04-27 | 2018-02-09 | 波士顿生物医药有限公司 | 用于使用stat3途径抑制剂和激酶抑制剂治疗癌症的方法 |
| US10377749B2 (en) | 2015-08-10 | 2019-08-13 | Sumitomo Dainippon Pharma Co., Ltd. | Purification method for 5-(thiazol-4-yl)indolin-2-one derivative |
| WO2017160978A1 (en) | 2016-03-15 | 2017-09-21 | Boston Biomedical, Inc. | Cell cultures and use thereof |
| JP2019519573A (ja) | 2016-06-28 | 2019-07-11 | ボストン バイオメディカル, インコーポレイテッド | がんを処置するための方法 |
| WO2018098352A2 (en) | 2016-11-22 | 2018-05-31 | Jun Oishi | Targeting kras induced immune checkpoint expression |
| JP7106563B2 (ja) | 2016-11-29 | 2022-07-26 | スミトモ ファーマ オンコロジー, インコーポレイテッド | ナフトフラン誘導体、その調製、および使用方法 |
| CN117224541A (zh) * | 2018-09-18 | 2023-12-15 | 北京强新生物科技有限公司 | 肥胖症的治疗 |
| MX2021003156A (es) * | 2018-09-18 | 2021-05-14 | 1 Globe Biomedical Co Ltd | Tratamiento para la enfermedad del higado graso no alcoholico. |
| CA3237696A1 (en) | 2021-11-08 | 2023-05-11 | Progentos Therapeutics, Inc. | Platelet-derived growth factor receptor (pdgfr) alpha inhibitors and uses thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999010325A1 (en) * | 1997-08-06 | 1999-03-04 | Glaxo Group Limited | Benzylidene-1,3-dihydro-indol-2-one derivatives as receptor tyrosine kinase inhibitors, particularly of raf kinases |
| WO1999015524A1 (en) * | 1997-09-23 | 1999-04-01 | Fujisawa Pharmaceutical Co., Ltd. | Thiazole derivatives |
| US20040043388A1 (en) * | 2001-03-02 | 2004-03-04 | Come Jon H. | Three hybrid assay system |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK0934937T3 (da) * | 1990-11-30 | 2002-04-02 | Otsuka Pharma Co Ltd | Azolderivater som superoxidradikalinhibitor |
| WO1998007695A1 (en) | 1996-08-23 | 1998-02-26 | Sugen, Inc. | Indolinone combinatorial libraries and related products and methods for the treatment of disease |
| SI1255752T1 (sl) * | 2000-02-15 | 2007-12-31 | Pharmacia & Upjohn Co Llc | S pirolom substituirani zaviralci 2-indolinon protein kinaza |
| ES2243461T3 (es) * | 2000-02-28 | 2005-12-01 | Sugen, Inc. | Compuestos de 3-(pirolillactona) -2-indolinona como inhibidores quinasa. |
| JP2003535847A (ja) * | 2000-06-02 | 2003-12-02 | スージェン・インコーポレーテッド | 蛋白質キナーゼ/ホスファターゼ阻害剤としてのインドリノン誘導体 |
| US6797725B2 (en) * | 2001-04-09 | 2004-09-28 | Sugen, Inc. | Prodrugs of a 3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives |
| US20030119839A1 (en) * | 2001-12-13 | 2003-06-26 | Nan-Horng Lin | Protein kinase inhibitors |
| SE0200979D0 (sv) * | 2002-03-28 | 2002-03-28 | Astrazeneca Ab | New compounds |
| US20050032871A1 (en) * | 2002-09-03 | 2005-02-10 | Sugen, Inc. | Sulfonylated pyrrole-2-indolinone derivatives as kinase inhibitors |
| JP2007509173A (ja) * | 2003-10-24 | 2007-04-12 | シエーリング アクチエンゲゼルシャフト | インドリノン誘導体類及び疾病状態、例えば癌の処理へのそれらの使用 |
| MX2008009557A (es) * | 2006-01-27 | 2009-01-07 | Shanghai Hengrui Pharm Co Ltd | Inhibidores de la cinasa de proteina de la pirrolo [3,2-c] piridin-4-ona-2-indolinona. |
| CN101679404B (zh) * | 2007-06-01 | 2012-06-13 | 霍夫曼-拉罗奇有限公司 | 哌啶-酰胺衍生物 |
| EP3037419B1 (en) * | 2007-09-06 | 2019-09-04 | Boston Biomedical, Inc. | Compositions of kinase inhibitors and their use for treatment of cancer and other diseases related to kinases |
| US9187454B2 (en) * | 2013-03-13 | 2015-11-17 | Boston Biomedical, Inc. | Inhibitors of kinases and cancer stem cells, and methods of preparation and use thereof |
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2008
- 2008-09-05 EP EP16156340.8A patent/EP3037419B1/en active Active
- 2008-09-05 PL PL08829600T patent/PL2197878T3/pl unknown
- 2008-09-05 JP JP2010524187A patent/JP5452490B2/ja not_active Expired - Fee Related
- 2008-09-05 HR HRP20161114TT patent/HRP20161114T1/hr unknown
- 2008-09-05 ES ES16156340T patent/ES2759347T3/es active Active
- 2008-09-05 DK DK08829600.9T patent/DK2197878T3/en active
- 2008-09-05 EP EP08829600.9A patent/EP2197878B1/en active Active
- 2008-09-05 CA CA2736177A patent/CA2736177A1/en not_active Abandoned
- 2008-09-05 HU HUE08829600A patent/HUE030774T2/hu unknown
- 2008-09-05 PT PT88296009T patent/PT2197878T/pt unknown
- 2008-09-05 SI SI200831667A patent/SI2197878T1/sl unknown
- 2008-09-05 ES ES08829600.9T patent/ES2591028T3/es active Active
- 2008-09-05 LT LTEP08829600.9T patent/LT2197878T/lt unknown
- 2008-09-05 US US12/676,869 patent/US8299106B2/en not_active Expired - Fee Related
- 2008-09-05 CN CN200880114705.9A patent/CN101848908B/zh active Active
- 2008-09-05 WO PCT/US2008/075418 patent/WO2009033033A2/en not_active Ceased
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2012
- 2012-08-27 US US13/595,708 patent/US20120321622A1/en not_active Abandoned
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2013
- 2013-12-27 JP JP2013272195A patent/JP5701372B2/ja not_active Expired - Fee Related
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2014
- 2014-07-29 US US14/445,783 patent/US9725444B2/en not_active Expired - Fee Related
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2015
- 2015-02-17 JP JP2015028165A patent/JP5974124B2/ja not_active Expired - Fee Related
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2016
- 2016-07-15 JP JP2016140101A patent/JP6495868B2/ja not_active Expired - Fee Related
- 2016-09-13 CY CY20161100904T patent/CY1118012T1/el unknown
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2017
- 2017-07-07 US US15/643,608 patent/US20180022743A1/en not_active Abandoned
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2018
- 2018-11-14 US US16/190,669 patent/US20190248781A1/en not_active Abandoned
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2019
- 2019-02-08 JP JP2019021397A patent/JP2019070051A/ja active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999010325A1 (en) * | 1997-08-06 | 1999-03-04 | Glaxo Group Limited | Benzylidene-1,3-dihydro-indol-2-one derivatives as receptor tyrosine kinase inhibitors, particularly of raf kinases |
| WO1999015524A1 (en) * | 1997-09-23 | 1999-04-01 | Fujisawa Pharmaceutical Co., Ltd. | Thiazole derivatives |
| US20040043388A1 (en) * | 2001-03-02 | 2004-03-04 | Come Jon H. | Three hybrid assay system |
Non-Patent Citations (1)
| Title |
|---|
| Karen Lackey, et al..The Discovery of Potent cRaf1 Kinase Inhibitors.《Bioorganic & Medicinal Chemistry Letters》.2000,第10卷223-226. * |
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