CN101652363B - 用作激酶抑制剂的噻唑基化合物 - Google Patents
用作激酶抑制剂的噻唑基化合物 Download PDFInfo
- Publication number
- CN101652363B CN101652363B CN2007800515523A CN200780051552A CN101652363B CN 101652363 B CN101652363 B CN 101652363B CN 2007800515523 A CN2007800515523 A CN 2007800515523A CN 200780051552 A CN200780051552 A CN 200780051552A CN 101652363 B CN101652363 B CN 101652363B
- Authority
- CN
- China
- Prior art keywords
- substituted
- ylamino
- pyridine
- ylthio
- alkyl
- 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.)
- Expired - Fee Related
Links
- 0 CCC*(*)C*(*)CCCC(CC**)CNc1ncc(Sc2c(*)c(C(NC(*)C(*)(*)*(*)*)=O)ncc2)[s]1 Chemical compound CCC*(*)C*(*)CCCC(CC**)CNc1ncc(Sc2c(*)c(C(NC(*)C(*)(*)*(*)*)=O)ncc2)[s]1 0.000 description 4
- WWLMLRCJVABRQL-UHFFFAOYSA-N CC(C)(C)CC(CN)(c1ccccc1)O Chemical compound CC(C)(C)CC(CN)(c1ccccc1)O WWLMLRCJVABRQL-UHFFFAOYSA-N 0.000 description 1
- SOKZKOSXMHBPLH-UHFFFAOYSA-N CC(C)(C)OC(NCC(CO)(c1ccccc1)c1ccccc1)=O Chemical compound CC(C)(C)OC(NCC(CO)(c1ccccc1)c1ccccc1)=O SOKZKOSXMHBPLH-UHFFFAOYSA-N 0.000 description 1
- XYAXBZVACNTJKM-UHFFFAOYSA-N CC(C)(C)OC(NCc1ccc(Nc2ncc(Sc(ccnc3C(O)=O)c3F)[s]2)nc1)=O Chemical compound CC(C)(C)OC(NCc1ccc(Nc2ncc(Sc(ccnc3C(O)=O)c3F)[s]2)nc1)=O XYAXBZVACNTJKM-UHFFFAOYSA-N 0.000 description 1
- JIAOOXVMPPXKCJ-UHFFFAOYSA-N CC1C=CC(C(CNC(c(nccc2Sc3cnc(Nc4ncccc4)[s]3)c2F)=O)(c2ccccc2)OC)=CC1 Chemical compound CC1C=CC(C(CNC(c(nccc2Sc3cnc(Nc4ncccc4)[s]3)c2F)=O)(c2ccccc2)OC)=CC1 JIAOOXVMPPXKCJ-UHFFFAOYSA-N 0.000 description 1
- RPHUFVYCFUSQLI-UHFFFAOYSA-N CCCC(CNC(c1nccc(Sc2cnc(Nc3ccccn3)[s]2)c1F)=O)(c1ccccc1)O Chemical compound CCCC(CNC(c1nccc(Sc2cnc(Nc3ccccn3)[s]2)c1F)=O)(c1ccccc1)O RPHUFVYCFUSQLI-UHFFFAOYSA-N 0.000 description 1
- ACICBMGSPRCCKE-UHFFFAOYSA-N COC(c1nccc(Sc2cnc(Nc(cc3)ncc3N)[s]2)c1)=O Chemical compound COC(c1nccc(Sc2cnc(Nc(cc3)ncc3N)[s]2)c1)=O ACICBMGSPRCCKE-UHFFFAOYSA-N 0.000 description 1
- YQMQTEJARSWZPZ-UHFFFAOYSA-N COc1cc(C(CN)O)ccc1 Chemical compound COc1cc(C(CN)O)ccc1 YQMQTEJARSWZPZ-UHFFFAOYSA-N 0.000 description 1
- ZOBWHQPVYLLSLN-UHFFFAOYSA-N Cc1cc(Nc2ncc(Sc3ccnc(C(NCC(C4OCCO4)(c4ccccc4)c4ccccc4)=O)c3F)[s]2)ncc1 Chemical compound Cc1cc(Nc2ncc(Sc3ccnc(C(NCC(C4OCCO4)(c4ccccc4)c4ccccc4)=O)c3F)[s]2)ncc1 ZOBWHQPVYLLSLN-UHFFFAOYSA-N 0.000 description 1
- LUUHJIZRTWHFHJ-UHFFFAOYSA-N Cc1cc(Nc2ncc(Sc3ccnc(C(NCC(C=O)(c4ccccc4)c4ccccc4)=O)c3F)[s]2)ncc1 Chemical compound Cc1cc(Nc2ncc(Sc3ccnc(C(NCC(C=O)(c4ccccc4)c4ccccc4)=O)c3F)[s]2)ncc1 LUUHJIZRTWHFHJ-UHFFFAOYSA-N 0.000 description 1
- GVMUXZIAKRZBPM-UHFFFAOYSA-N Cc1cc(Nc2ncc(Sc3ccnc(C(NCC(CN(C)C)(c4ccccc4)c4ccccc4)=O)c3F)[s]2)ncc1 Chemical compound Cc1cc(Nc2ncc(Sc3ccnc(C(NCC(CN(C)C)(c4ccccc4)c4ccccc4)=O)c3F)[s]2)ncc1 GVMUXZIAKRZBPM-UHFFFAOYSA-N 0.000 description 1
- CXIZDQBPESYGCZ-UHFFFAOYSA-N Cc1cc(Nc2ncc(Sc3ccnc(C(NCC(c4ccccc4)c4c(COCOC)cccc4)=O)c3F)[s]2)ncc1 Chemical compound Cc1cc(Nc2ncc(Sc3ccnc(C(NCC(c4ccccc4)c4c(COCOC)cccc4)=O)c3F)[s]2)ncc1 CXIZDQBPESYGCZ-UHFFFAOYSA-N 0.000 description 1
- FGUAAEQNOXYNDU-UHFFFAOYSA-N Cc1ccnc(Nc2ncc(Sc3ccnc(C(NCC(c4ccccc4)(c4ccccc4)O)=O)c3F)[s]2)c1 Chemical compound Cc1ccnc(Nc2ncc(Sc3ccnc(C(NCC(c4ccccc4)(c4ccccc4)O)=O)c3F)[s]2)c1 FGUAAEQNOXYNDU-UHFFFAOYSA-N 0.000 description 1
- QFWZRNZLPMDFNA-UHFFFAOYSA-N NCC(c1ccccc1)(c1ccccc1)O Chemical compound NCC(c1ccccc1)(c1ccccc1)O QFWZRNZLPMDFNA-UHFFFAOYSA-N 0.000 description 1
- BERVRRDRXOQROW-UHFFFAOYSA-N O=C(c1nccc(Sc2cnc(Nc3ncccc3)[s]2)c1)NCC1(c2ccccc2)OCCO1 Chemical compound O=C(c1nccc(Sc2cnc(Nc3ncccc3)[s]2)c1)NCC1(c2ccccc2)OCCO1 BERVRRDRXOQROW-UHFFFAOYSA-N 0.000 description 1
- YJZCYXXYAVVSGC-UHFFFAOYSA-N OC(CNC(c1nccc(Sc2cnc(Nc3ncccc3)[s]2)c1)=O)(c1ccccc1)c1ccccc1 Chemical compound OC(CNC(c1nccc(Sc2cnc(Nc3ncccc3)[s]2)c1)=O)(c1ccccc1)c1ccccc1 YJZCYXXYAVVSGC-UHFFFAOYSA-N 0.000 description 1
- WAALMHQZCVYFGI-UHFFFAOYSA-N OCC(CNC(c1cc(Sc2cnc(Nc(cc3)ncc3NC3CCNCC3)[s]2)ccn1)=O)(c1ccccc1)c1ccccc1 Chemical compound OCC(CNC(c1cc(Sc2cnc(Nc(cc3)ncc3NC3CCNCC3)[s]2)ccn1)=O)(c1ccccc1)c1ccccc1 WAALMHQZCVYFGI-UHFFFAOYSA-N 0.000 description 1
- IFBXWLONWUZDID-UHFFFAOYSA-N OCc1c(C(CNC(c(nccc2Sc3cnc(Nc4ccccn4)[s]3)c2F)=O)c2ccccc2)cccc1 Chemical compound OCc1c(C(CNC(c(nccc2Sc3cnc(Nc4ccccn4)[s]3)c2F)=O)c2ccccc2)cccc1 IFBXWLONWUZDID-UHFFFAOYSA-N 0.000 description 1
- IFBXWLONWUZDID-QFIPXVFZSA-N OCc1c([C@@H](CNC(c(nccc2Sc3cnc(Nc4[n]cccc4)[s]3)c2F)=O)c2ccccc2)cccc1 Chemical compound OCc1c([C@@H](CNC(c(nccc2Sc3cnc(Nc4[n]cccc4)[s]3)c2F)=O)c2ccccc2)cccc1 IFBXWLONWUZDID-QFIPXVFZSA-N 0.000 description 1
Classifications
-
- 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
- C07D417/14—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
-
- 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
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (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)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87087206P | 2006-12-20 | 2006-12-20 | |
| US60/870,872 | 2006-12-20 | ||
| PCT/US2007/088124 WO2008079873A2 (en) | 2006-12-20 | 2007-12-19 | Thiazolyl compounds useful as kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101652363A CN101652363A (zh) | 2010-02-17 |
| CN101652363B true CN101652363B (zh) | 2013-04-17 |
Family
ID=39563189
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2007800515523A Expired - Fee Related CN101652363B (zh) | 2006-12-20 | 2007-12-19 | 用作激酶抑制剂的噻唑基化合物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8148400B2 (OSRAM) |
| EP (1) | EP2099794B1 (OSRAM) |
| JP (1) | JP5225288B2 (OSRAM) |
| CN (1) | CN101652363B (OSRAM) |
| NO (1) | NO20092035L (OSRAM) |
| WO (1) | WO2008079873A2 (OSRAM) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8343999B2 (en) * | 2007-04-10 | 2013-01-01 | Bristol-Myers Squibb Company | Thiazolyl compounds useful as kinase inhibitors |
| EP2559771A3 (en) | 2007-05-17 | 2013-06-12 | Bristol-Myers Squibb Company | Biomarkers and methods for determining sensitivity to insulin growth factor-1 receptor modulators |
| US9180127B2 (en) | 2009-12-29 | 2015-11-10 | Dana-Farber Cancer Institute, Inc. | Type II Raf kinase inhibitors |
| CN102070518B (zh) * | 2011-01-24 | 2012-05-02 | 江苏先声药物研究有限公司 | 取代吡啶及氮杂吲哚衍生物的合成 |
| WO2015154022A1 (en) * | 2014-04-05 | 2015-10-08 | Syros Pharmaceuticals, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
| HK1245260A1 (zh) | 2014-12-23 | 2018-08-24 | Dana-Farber Cancer Institute, Inc. | 细胞周期蛋白依赖性激酶7(cdk7)的抑制剂 |
| JP6861166B2 (ja) | 2015-03-27 | 2021-04-21 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | サイクリン依存性キナーゼの阻害剤 |
| US11142507B2 (en) | 2015-09-09 | 2021-10-12 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinases |
| CN106932502B (zh) * | 2015-12-31 | 2021-05-18 | 上海奥博生物医药股份有限公司 | 一种索拉菲尼中4-氯-2-吡啶甲酸甲酯含量的测定方法 |
| CN107043375B (zh) * | 2017-04-28 | 2020-03-20 | 江苏食品药品职业技术学院 | 一种制备达沙替尼及其中间体的新方法 |
| EP3810132A4 (en) | 2018-06-25 | 2022-06-22 | Dana-Farber Cancer Institute, Inc. | TAIRE FAMILY KINASE INHIBITORS AND RELATED USES |
| KR102253652B1 (ko) * | 2019-08-19 | 2021-05-18 | 주식회사 셀젠텍 | 신규한 암전이 억제 활성을 갖는 화합물, 이의 제조방법 및 상기 화합물을 포함하는 암 전이 및 침윤 억제, 또는 암 치료용 약학적 조성물 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030069238A1 (en) * | 2000-12-21 | 2003-04-10 | Barrish Joel C. | Thiazolyl inhibitors of Tec family tyrosine kinases |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE602004028907D1 (de) * | 2003-02-06 | 2010-10-14 | Bristol Myers Squibb Co | Als kinaseinhibitoren geeignete verbindungen auf thiazolylbasis |
| US8343999B2 (en) * | 2007-04-10 | 2013-01-01 | Bristol-Myers Squibb Company | Thiazolyl compounds useful as kinase inhibitors |
-
2007
- 2007-12-19 US US12/519,597 patent/US8148400B2/en active Active
- 2007-12-19 JP JP2009543183A patent/JP5225288B2/ja not_active Expired - Fee Related
- 2007-12-19 EP EP07869520.2A patent/EP2099794B1/en active Active
- 2007-12-19 WO PCT/US2007/088124 patent/WO2008079873A2/en not_active Ceased
- 2007-12-19 CN CN2007800515523A patent/CN101652363B/zh not_active Expired - Fee Related
-
2009
- 2009-05-26 NO NO20092035A patent/NO20092035L/no not_active Application Discontinuation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030069238A1 (en) * | 2000-12-21 | 2003-04-10 | Barrish Joel C. | Thiazolyl inhibitors of Tec family tyrosine kinases |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008079873A2 (en) | 2008-07-03 |
| US8148400B2 (en) | 2012-04-03 |
| NO20092035L (no) | 2009-07-15 |
| JP2010514686A (ja) | 2010-05-06 |
| EP2099794B1 (en) | 2013-05-15 |
| CN101652363A (zh) | 2010-02-17 |
| US20100048581A1 (en) | 2010-02-25 |
| EP2099794A2 (en) | 2009-09-16 |
| WO2008079873A3 (en) | 2008-10-02 |
| JP5225288B2 (ja) | 2013-07-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20130417 Termination date: 20141219 |
|
| EXPY | Termination of patent right or utility model |