CN104334532B - 异喹啉和二氮杂萘衍生物 - Google Patents
异喹啉和二氮杂萘衍生物 Download PDFInfo
- Publication number
- CN104334532B CN104334532B CN201380013877.8A CN201380013877A CN104334532B CN 104334532 B CN104334532 B CN 104334532B CN 201380013877 A CN201380013877 A CN 201380013877A CN 104334532 B CN104334532 B CN 104334532B
- Authority
- CN
- China
- Prior art keywords
- alkyl
- substituted
- heterocyclyl
- compound
- unsubstituted
- 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 *NC(c(c(cc1)c2nc1C1=CC(F)=NC#CC1)cnc2N)=O Chemical compound *NC(c(c(cc1)c2nc1C1=CC(F)=NC#CC1)cnc2N)=O 0.000 description 7
- GUBZXYDMHCAWAK-UHFFFAOYSA-N Nc1ncc(-c2c[n](CCN3CCOCC3)cn2)c(cc2)c1nc2-c1cccc(F)c1 Chemical compound Nc1ncc(-c2c[n](CCN3CCOCC3)cn2)c(cc2)c1nc2-c1cccc(F)c1 GUBZXYDMHCAWAK-UHFFFAOYSA-N 0.000 description 2
- BPIZCCUYPZWLGA-UHFFFAOYSA-N Nc1ncc(C(O)=O)c(cc2)c1nc2-c1cccc(F)c1 Chemical compound Nc1ncc(C(O)=O)c(cc2)c1nc2-c1cccc(F)c1 BPIZCCUYPZWLGA-UHFFFAOYSA-N 0.000 description 2
- XHQZJHWRKZULCD-UHFFFAOYSA-N Bc1c[n](CCN2CCOCC2)cn1 Chemical compound Bc1c[n](CCN2CCOCC2)cn1 XHQZJHWRKZULCD-UHFFFAOYSA-N 0.000 description 1
- QYPUYELCXOGOGM-WZUFQYTHSA-N C=C/C=C(/c1cccc(F)c1)\N=C Chemical compound C=C/C=C(/c1cccc(F)c1)\N=C QYPUYELCXOGOGM-WZUFQYTHSA-N 0.000 description 1
- HXQDOCDYYZIBSC-UHFFFAOYSA-N CC(C)(C)OC(N(C(OC(C)(C)C)=O)c1ncc(B2OC(C)(C)C(C)(C)O2)c(cc2)c1nc2-c1cccc(F)c1)O Chemical compound CC(C)(C)OC(N(C(OC(C)(C)C)=O)c1ncc(B2OC(C)(C)C(C)(C)O2)c(cc2)c1nc2-c1cccc(F)c1)O HXQDOCDYYZIBSC-UHFFFAOYSA-N 0.000 description 1
- RSAUMXIATNWZDO-UHFFFAOYSA-N CC(C)(C)OC(NC(C1)CN1C(c(c(cc1)c2nc1-c1cccc(F)c1)cnc2N)=O)=O Chemical compound CC(C)(C)OC(NC(C1)CN1C(c(c(cc1)c2nc1-c1cccc(F)c1)cnc2N)=O)=O RSAUMXIATNWZDO-UHFFFAOYSA-N 0.000 description 1
- DACFTWKQEUYESJ-UHFFFAOYSA-N CC(C)(C)OC(Nc1ncc(-c2c[n](CCN3CCOCC3)cn2)c(cc2)c1nc2-c1cccc(F)c1)=O Chemical compound CC(C)(C)OC(Nc1ncc(-c2c[n](CCN3CCOCC3)cn2)c(cc2)c1nc2-c1cccc(F)c1)=O DACFTWKQEUYESJ-UHFFFAOYSA-N 0.000 description 1
- ZQBJAGLSXOHJNL-UHFFFAOYSA-N CC(C)(CNC(c1c(ccc(-c2cccc(F)c2)c2)c2c(N)nc1)O)N Chemical compound CC(C)(CNC(c1c(ccc(-c2cccc(F)c2)c2)c2c(N)nc1)O)N ZQBJAGLSXOHJNL-UHFFFAOYSA-N 0.000 description 1
- BNPSUOBVONIZFJ-UHFFFAOYSA-N CC(c1c(ccc(-c2cccc(F)c2)c2)c2c(N)nc1)N Chemical compound CC(c1c(ccc(-c2cccc(F)c2)c2)c2c(N)nc1)N BNPSUOBVONIZFJ-UHFFFAOYSA-N 0.000 description 1
- ZUQYNQZMIYRLFK-UHFFFAOYSA-N CC1C(c(cc2)nc3c2c(I)cnc3N(C(OCC(C)(C)C)=O)C(OCC(C)(C)C)=O)=CC(F)=CC1 Chemical compound CC1C(c(cc2)nc3c2c(I)cnc3N(C(OCC(C)(C)C)=O)C(OCC(C)(C)C)=O)=CC(F)=CC1 ZUQYNQZMIYRLFK-UHFFFAOYSA-N 0.000 description 1
- YTBGPUKLAPQATG-UHFFFAOYSA-N CCOC(c(c(cc1)c2nc1-c1ccnc(F)c1)cnc2N)=O Chemical compound CCOC(c(c(cc1)c2nc1-c1ccnc(F)c1)cnc2N)=O YTBGPUKLAPQATG-UHFFFAOYSA-N 0.000 description 1
- RPBTWEXKEQCSHJ-YFKPBYRVSA-N CC[C@@H](N)NC=C Chemical compound CC[C@@H](N)NC=C RPBTWEXKEQCSHJ-YFKPBYRVSA-N 0.000 description 1
- PSLCTXYRMODTDI-UHFFFAOYSA-N CNC(C(C1)OCCN1C(c1c(ccc(-c2cccc(F)c2)c2)c2c(N)nc1)O)=O Chemical compound CNC(C(C1)OCCN1C(c1c(ccc(-c2cccc(F)c2)c2)c2c(N)nc1)O)=O PSLCTXYRMODTDI-UHFFFAOYSA-N 0.000 description 1
- FIJGHAFRTNMLSO-UHFFFAOYSA-N COC(N)NC=C Chemical compound COC(N)NC=C FIJGHAFRTNMLSO-UHFFFAOYSA-N 0.000 description 1
- XCQWMIWCZDNOMT-UHFFFAOYSA-N Cc(c(-c(cc1)nc2c1c(C(NC(C1)CN1C(C1CC1)=O)=O)cnc2N)ccc1)c1F Chemical compound Cc(c(-c(cc1)nc2c1c(C(NC(C1)CN1C(C1CC1)=O)=O)cnc2N)ccc1)c1F XCQWMIWCZDNOMT-UHFFFAOYSA-N 0.000 description 1
- GXXKGRKAYKMGDH-UHFFFAOYSA-N Cc(c(cc1)c2nc1-c1cccc(F)c1)cnc2N Chemical compound Cc(c(cc1)c2nc1-c1cccc(F)c1)cnc2N GXXKGRKAYKMGDH-UHFFFAOYSA-N 0.000 description 1
- DJQKRSCDLXWYLQ-UHFFFAOYSA-N NC(C1)CN1C(C(C1C=C2)C=NC(N)=C1N=C2c1cccc(F)c1)=O Chemical compound NC(C1)CN1C(C(C1C=C2)C=NC(N)=C1N=C2c1cccc(F)c1)=O DJQKRSCDLXWYLQ-UHFFFAOYSA-N 0.000 description 1
- QEYQLSDFQMDPRE-UHFFFAOYSA-N NC(C1)CN1C(C1CC1)=O Chemical compound NC(C1)CN1C(C1CC1)=O QEYQLSDFQMDPRE-UHFFFAOYSA-N 0.000 description 1
- XRMAMAPOXZCXRG-UHFFFAOYSA-N NC(C1)CN1S(C(F)(F)F)(=O)=O Chemical compound NC(C1)CN1S(C(F)(F)F)(=O)=O XRMAMAPOXZCXRG-UHFFFAOYSA-N 0.000 description 1
- NJIDZESSQSYECQ-UHFFFAOYSA-N NC(c1nc(CNC(c2c(ccc(-c3cccc(F)c3)c3)c3c(N)nc2)O)n[o]1)=O Chemical compound NC(c1nc(CNC(c2c(ccc(-c3cccc(F)c3)c3)c3c(N)nc2)O)n[o]1)=O NJIDZESSQSYECQ-UHFFFAOYSA-N 0.000 description 1
- WVFFPWADHJVCRB-UHFFFAOYSA-N Nc(nc1)c(cc(cc2)-c3cc(F)ccc3)c2c1C(NCCCN1CCOCC1)=O Chemical compound Nc(nc1)c(cc(cc2)-c3cc(F)ccc3)c2c1C(NCCCN1CCOCC1)=O WVFFPWADHJVCRB-UHFFFAOYSA-N 0.000 description 1
- OJDRDHMMUDJQBJ-UHFFFAOYSA-N Nc(nc1)c(cc(cc2)-c3cccc(F)c3)c2c1C(NCC1COCC1)=O Chemical compound Nc(nc1)c(cc(cc2)-c3cccc(F)c3)c2c1C(NCC1COCC1)=O OJDRDHMMUDJQBJ-UHFFFAOYSA-N 0.000 description 1
- YCXMTNJCODWPFI-UHFFFAOYSA-N Nc(nc1)c(cc(cc2)-c3cccc(F)c3)c2c1C(Nc1ccccc1)=O Chemical compound Nc(nc1)c(cc(cc2)-c3cccc(F)c3)c2c1C(Nc1ccccc1)=O YCXMTNJCODWPFI-UHFFFAOYSA-N 0.000 description 1
- GAOIMHWGJPKSMR-UHFFFAOYSA-N Nc1ncc(C(N(C2)CC2N(C(C2CC2)=O)C(C2CC2)=O)=O)c(cc2)c1nc2-c1cccc(F)c1 Chemical compound Nc1ncc(C(N(C2)CC2N(C(C2CC2)=O)C(C2CC2)=O)=O)c(cc2)c1nc2-c1cccc(F)c1 GAOIMHWGJPKSMR-UHFFFAOYSA-N 0.000 description 1
- BDJNMHHFCPYIGC-UHFFFAOYSA-N Nc1ncc(C(NC(C2)CN2C(C2CC2)=O)=O)c(cc2)c1nc2-c1ccnc(F)c1 Chemical compound Nc1ncc(C(NC(C2)CN2C(C2CC2)=O)=O)c(cc2)c1nc2-c1ccnc(F)c1 BDJNMHHFCPYIGC-UHFFFAOYSA-N 0.000 description 1
- FUJRXIRWLOEMDU-UHFFFAOYSA-N Nc1ncc(C(O)=O)c(cc2)c1nc2-c1ccnc(F)c1 Chemical compound Nc1ncc(C(O)=O)c(cc2)c1nc2-c1ccnc(F)c1 FUJRXIRWLOEMDU-UHFFFAOYSA-N 0.000 description 1
- WZNZRAABYBUVOT-UHFFFAOYSA-M [NH-]c(nc1)c(cc(cc2)C(C=CC3)=CC3F)c2c1C(N1CCN(CCO)CC1)=O Chemical compound [NH-]c(nc1)c(cc(cc2)C(C=CC3)=CC3F)c2c1C(N1CCN(CCO)CC1)=O WZNZRAABYBUVOT-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
- C07D217/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D401/06—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 only aliphatic carbon atoms
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261592443P | 2012-01-30 | 2012-01-30 | |
| US61/592,443 | 2012-01-30 | ||
| US201261593775P | 2012-02-01 | 2012-02-01 | |
| US61/593,775 | 2012-02-01 | ||
| US201261701916P | 2012-09-17 | 2012-09-17 | |
| US61/701,916 | 2012-09-17 | ||
| PCT/EP2013/051613 WO2013113669A1 (en) | 2012-01-30 | 2013-01-29 | Isoquinoline and naphthyridine derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104334532A CN104334532A (zh) | 2015-02-04 |
| CN104334532B true CN104334532B (zh) | 2018-08-14 |
Family
ID=47666117
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201380013877.8A Expired - Fee Related CN104334532B (zh) | 2012-01-30 | 2013-01-29 | 异喹啉和二氮杂萘衍生物 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9586956B2 (https=) |
| EP (1) | EP2809652B1 (https=) |
| JP (1) | JP6363020B2 (https=) |
| KR (1) | KR20140117651A (https=) |
| CN (1) | CN104334532B (https=) |
| BR (1) | BR112014018670A8 (https=) |
| CA (1) | CA2863132A1 (https=) |
| MX (1) | MX353190B (https=) |
| RU (1) | RU2014133390A (https=) |
| WO (1) | WO2013113669A1 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016511237A (ja) * | 2013-02-01 | 2016-04-14 | アセチロン ファーマシューティカルズ インコーポレイテッドAcetylon Pharmaceuticals,Inc. | 選択的hdac3阻害剤 |
| WO2016114816A1 (en) * | 2015-01-18 | 2016-07-21 | Sri International | MAP4K4 (HGK) Inhibitors |
| AU2018347783B2 (en) * | 2017-10-13 | 2023-03-16 | Imperial College Innovations Limited | MAP4K4 inhibitors |
| GB201819839D0 (en) | 2018-12-05 | 2019-01-23 | Imperial Innovations Ltd | MAP4K4 inhibitors |
| CN110066259A (zh) * | 2019-05-22 | 2019-07-30 | 南京合巨药业有限公司 | 一种n-环戊基-1,1-二氧代-4-硫代吗啉甲酰胺的合成方法 |
| CN110028432A (zh) * | 2019-05-22 | 2019-07-19 | 南京合巨药业有限公司 | 一种(3-氨基-氮杂环丁烷-1-基)-环丙基-甲酮的制备方法 |
| GB201915829D0 (en) * | 2019-10-31 | 2019-12-18 | Cancer Research Tech Ltd | Compounds, compositions and therapeutic uses thereof |
| GB201915831D0 (en) * | 2019-10-31 | 2019-12-18 | Cancer Research Tech Ltd | Compounds, compositions and therapeutic uses thereof |
| WO2022150962A1 (en) * | 2021-01-12 | 2022-07-21 | Westlake Pharmaceutical (Hangzhou) Co., Ltd. | Protease inhibitors, preparation, and uses thereof |
| CN117279896A (zh) * | 2021-04-07 | 2023-12-22 | 劲方医药科技(上海)有限公司 | 氨基取代的吡啶并环类化合物及其制法和用途 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101641351A (zh) * | 2006-12-21 | 2010-02-03 | 普莱希科公司 | 用于激酶调节的化合物和方法及其适应症 |
| CN101668757A (zh) * | 2006-12-21 | 2010-03-10 | 普莱希科公司 | 作为激酶调节剂的吡咯并[2,3-b]吡啶衍生物 |
| WO2010111527A1 (en) * | 2009-03-26 | 2010-09-30 | Plexxikon, Inc. | Pyrazolo [ 3, 4 -b] pyridines as kinase inhibitors and their medical use |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3773919A (en) | 1969-10-23 | 1973-11-20 | Du Pont | Polylactide-drug mixtures |
| AU776962B2 (en) * | 1999-04-21 | 2004-09-30 | Wyeth Holdings Corporation | Substituted 3-cyano-(1.7), (1.5), and (1.8)-naphthyridine inhibitors of tyrosine kinases |
| AR045944A1 (es) * | 2003-09-24 | 2005-11-16 | Novartis Ag | Derivados de isoquinolina 1.4-disustituidas |
-
2013
- 2013-01-29 RU RU2014133390A patent/RU2014133390A/ru not_active Application Discontinuation
- 2013-01-29 MX MX2014009180A patent/MX353190B/es active IP Right Grant
- 2013-01-29 CN CN201380013877.8A patent/CN104334532B/zh not_active Expired - Fee Related
- 2013-01-29 BR BR112014018670A patent/BR112014018670A8/pt not_active IP Right Cessation
- 2013-01-29 EP EP13702781.9A patent/EP2809652B1/en active Active
- 2013-01-29 KR KR1020147024093A patent/KR20140117651A/ko not_active Withdrawn
- 2013-01-29 CA CA2863132A patent/CA2863132A1/en not_active Abandoned
- 2013-01-29 JP JP2014553751A patent/JP6363020B2/ja not_active Expired - Fee Related
- 2013-01-29 WO PCT/EP2013/051613 patent/WO2013113669A1/en not_active Ceased
-
2014
- 2014-07-31 US US14/448,941 patent/US9586956B2/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101641351A (zh) * | 2006-12-21 | 2010-02-03 | 普莱希科公司 | 用于激酶调节的化合物和方法及其适应症 |
| CN101668757A (zh) * | 2006-12-21 | 2010-03-10 | 普莱希科公司 | 作为激酶调节剂的吡咯并[2,3-b]吡啶衍生物 |
| WO2010111527A1 (en) * | 2009-03-26 | 2010-09-30 | Plexxikon, Inc. | Pyrazolo [ 3, 4 -b] pyridines as kinase inhibitors and their medical use |
Also Published As
| Publication number | Publication date |
|---|---|
| CN104334532A (zh) | 2015-02-04 |
| US20140343036A1 (en) | 2014-11-20 |
| MX353190B (es) | 2018-01-05 |
| EP2809652A1 (en) | 2014-12-10 |
| RU2014133390A (ru) | 2016-03-20 |
| US9586956B2 (en) | 2017-03-07 |
| JP2015509921A (ja) | 2015-04-02 |
| WO2013113669A1 (en) | 2013-08-08 |
| HK1202291A1 (en) | 2015-09-25 |
| BR112014018670A8 (pt) | 2017-07-11 |
| MX2014009180A (es) | 2014-10-13 |
| BR112014018670A2 (https=) | 2017-06-20 |
| JP6363020B2 (ja) | 2018-07-25 |
| CA2863132A1 (en) | 2013-08-08 |
| KR20140117651A (ko) | 2014-10-07 |
| EP2809652B1 (en) | 2019-05-15 |
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