JP5746015B2 - Axlキナーゼ阻害剤としてのキノリン誘導体 - Google Patents
Axlキナーゼ阻害剤としてのキノリン誘導体 Download PDFInfo
- Publication number
- JP5746015B2 JP5746015B2 JP2011504377A JP2011504377A JP5746015B2 JP 5746015 B2 JP5746015 B2 JP 5746015B2 JP 2011504377 A JP2011504377 A JP 2011504377A JP 2011504377 A JP2011504377 A JP 2011504377A JP 5746015 B2 JP5746015 B2 JP 5746015B2
- Authority
- JP
- Japan
- Prior art keywords
- quinolin
- yloxy
- phenyl
- fluoro
- benzenesulfonamide
- 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.)
- Active
Links
- IBXYLWORFFCGIO-UHFFFAOYSA-N CC(Nc(ccc(C)c1)c1S(Nc(cc1)ccc1Oc1c(cc(c(OC)c2)OC)c2ncc1)(=O)=O)=O Chemical compound CC(Nc(ccc(C)c1)c1S(Nc(cc1)ccc1Oc1c(cc(c(OC)c2)OC)c2ncc1)(=O)=O)=O IBXYLWORFFCGIO-UHFFFAOYSA-N 0.000 description 1
- LCVQVBQTRQBYFW-UHFFFAOYSA-N CC1CCN(CCCOc2cc3nccc(Oc(ccc(NS(c(cccc4)c4OC(F)(F)F)(=O)=O)c4)c4F)c3cc2OC)CC1 Chemical compound CC1CCN(CCCOc2cc3nccc(Oc(ccc(NS(c(cccc4)c4OC(F)(F)F)(=O)=O)c4)c4F)c3cc2OC)CC1 LCVQVBQTRQBYFW-UHFFFAOYSA-N 0.000 description 1
- BXANXSCLEFFIFT-UHFFFAOYSA-N CC1CCN(CCCOc2cc3nccc(Oc(ccc(NS(c4c(cccc5)c5ccc4)(=O)=O)c4)c4F)c3cc2OC)CC1 Chemical compound CC1CCN(CCCOc2cc3nccc(Oc(ccc(NS(c4c(cccc5)c5ccc4)(=O)=O)c4)c4F)c3cc2OC)CC1 BXANXSCLEFFIFT-UHFFFAOYSA-N 0.000 description 1
- WATLMELLJSACHR-UHFFFAOYSA-N CCC(C1)C(Oc2c(cc(c(OC)c3)OC)c3ncc2)=CC=C1NS(C(CCC=C1)=C1OC(F)(F)F)(=O)=O Chemical compound CCC(C1)C(Oc2c(cc(c(OC)c3)OC)c3ncc2)=CC=C1NS(C(CCC=C1)=C1OC(F)(F)F)(=O)=O WATLMELLJSACHR-UHFFFAOYSA-N 0.000 description 1
- HOHWDGKXGPAZTP-UHFFFAOYSA-N CN(C(C1)=O)c(cc2)c1cc2S(Nc(c(F)c1)ccc1Oc1c(cc(c(OC)c2)OC)c2ncc1)(=O)=O Chemical compound CN(C(C1)=O)c(cc2)c1cc2S(Nc(c(F)c1)ccc1Oc1c(cc(c(OC)c2)OC)c2ncc1)(=O)=O HOHWDGKXGPAZTP-UHFFFAOYSA-N 0.000 description 1
- BXPJZJZHJMQLHL-UHFFFAOYSA-N COC(C(C1)C1(C1=C2)N=CC=C1Oc(cc1)ccc1NS(c(cc1Cl)cc(Cl)c1O)(=O)=O)=C2OC Chemical compound COC(C(C1)C1(C1=C2)N=CC=C1Oc(cc1)ccc1NS(c(cc1Cl)cc(Cl)c1O)(=O)=O)=C2OC BXPJZJZHJMQLHL-UHFFFAOYSA-N 0.000 description 1
- YZCGMEXIRHDPMN-QPSGOUHRSA-N COC(CC(C(/C(/Oc(cc1)cc(F)c1NS(c1c(C(F)(F)F)cccc1)(=O)=O)=C\C=C)=C1)N)=C1OC Chemical compound COC(CC(C(/C(/Oc(cc1)cc(F)c1NS(c1c(C(F)(F)F)cccc1)(=O)=O)=C\C=C)=C1)N)=C1OC YZCGMEXIRHDPMN-QPSGOUHRSA-N 0.000 description 1
- IUYWIDRRRPUDQS-UHFFFAOYSA-N COC(CC(C1=C2)N=CC=C1OC(C(C1)F)=CC=C1NS(c1c(cccc3)c3ccc1)(=O)=O)=C2OC Chemical compound COC(CC(C1=C2)N=CC=C1OC(C(C1)F)=CC=C1NS(c1c(cccc3)c3ccc1)(=O)=O)=C2OC IUYWIDRRRPUDQS-UHFFFAOYSA-N 0.000 description 1
- PBXZJADXJUNYBZ-UHFFFAOYSA-N COC(CC(C1=C2)N=CC=C1OC1C(OC)=CC(NS(c3c(C(F)(F)F)cccc3)(=O)=O)=CC1)=C2OC Chemical compound COC(CC(C1=C2)N=CC=C1OC1C(OC)=CC(NS(c3c(C(F)(F)F)cccc3)(=O)=O)=CC1)=C2OC PBXZJADXJUNYBZ-UHFFFAOYSA-N 0.000 description 1
- KXLYJQDWZISGPS-UHFFFAOYSA-N COc(c(OC)c1)cc2c1nccc2Oc(cc1F)ccc1NS(c1cc(-c2ncccn2)ccc1)(=O)=O Chemical compound COc(c(OC)c1)cc2c1nccc2Oc(cc1F)ccc1NS(c1cc(-c2ncccn2)ccc1)(=O)=O KXLYJQDWZISGPS-UHFFFAOYSA-N 0.000 description 1
- MTUSRYUTUQTLMP-UHFFFAOYSA-N COc(c(OC)cc1ncc2)cc1c2Oc(cc1)cc(F)c1NS(c(cc1OC)ccc1F)(=O)=O Chemical compound COc(c(OC)cc1ncc2)cc1c2Oc(cc1)cc(F)c1NS(c(cc1OC)ccc1F)(=O)=O MTUSRYUTUQTLMP-UHFFFAOYSA-N 0.000 description 1
- VTGHKOZVNANOGW-UHFFFAOYSA-N COc(c(OC)cc1ncc2)cc1c2Oc(cc1)cc(F)c1NS(c1cc(F)cc(F)c1)(OC)=O Chemical compound COc(c(OC)cc1ncc2)cc1c2Oc(cc1)cc(F)c1NS(c1cc(F)cc(F)c1)(OC)=O VTGHKOZVNANOGW-UHFFFAOYSA-N 0.000 description 1
- CQTPKIQGFCRYMU-UHFFFAOYSA-N COc(c(OC)cc1ncc2)cc1c2Oc(cc1F)ccc1NS(c(cc(C(F)(F)F)cc1)c1Br)(=O)=O Chemical compound COc(c(OC)cc1ncc2)cc1c2Oc(cc1F)ccc1NS(c(cc(C(F)(F)F)cc1)c1Br)(=O)=O CQTPKIQGFCRYMU-UHFFFAOYSA-N 0.000 description 1
- UGQAGPROPDCARW-UHFFFAOYSA-N COc(c(OC)cc1ncc2)cc1c2Oc(cc1F)ccc1NS(c(cccc1)c1Br)(=O)=O Chemical compound COc(c(OC)cc1ncc2)cc1c2Oc(cc1F)ccc1NS(c(cccc1)c1Br)(=O)=O UGQAGPROPDCARW-UHFFFAOYSA-N 0.000 description 1
- CBVVVTFKIHGNOV-UHFFFAOYSA-N COc(c(OC)cc1ncc2)cc1c2Oc(cc1F)ccc1NS(c1cccc(OC(F)(F)F)c1)(=O)=O Chemical compound COc(c(OC)cc1ncc2)cc1c2Oc(cc1F)ccc1NS(c1cccc(OC(F)(F)F)c1)(=O)=O CBVVVTFKIHGNOV-UHFFFAOYSA-N 0.000 description 1
- AARSULSMMPXIQK-UHFFFAOYSA-N COc(c(OC)cc1ncc2)cc1c2Oc(ccc(NS(C1=C(C(F)(F)F)C=CCC1)(=O)=O)c1)c1F Chemical compound COc(c(OC)cc1ncc2)cc1c2Oc(ccc(NS(C1=C(C(F)(F)F)C=CCC1)(=O)=O)c1)c1F AARSULSMMPXIQK-UHFFFAOYSA-N 0.000 description 1
- JLJYBNBKBKTOPB-UHFFFAOYSA-N COc(c(OCCCN1CCOCC1)cc1ncc2)cc1c2Oc(ccc(NS(c(cccc1)c1F)(=O)=O)c1)c1F Chemical compound COc(c(OCCCN1CCOCC1)cc1ncc2)cc1c2Oc(ccc(NS(c(cccc1)c1F)(=O)=O)c1)c1F JLJYBNBKBKTOPB-UHFFFAOYSA-N 0.000 description 1
- BHPIKIXAVMHPPZ-UHFFFAOYSA-N COc(c(OCCCN1CCOCC1)cc1ncc2)cc1c2Oc(ccc(NS(c1c(cccc2)c2ccc1)(=O)=O)c1)c1F Chemical compound COc(c(OCCCN1CCOCC1)cc1ncc2)cc1c2Oc(ccc(NS(c1c(cccc2)c2ccc1)(=O)=O)c1)c1F BHPIKIXAVMHPPZ-UHFFFAOYSA-N 0.000 description 1
- DFLWWSFMWUEGDL-UHFFFAOYSA-N COc(c(OCc1ccccc1)cc1ncc2)cc1c2Oc(cc1F)ccc1NS(c1cc(-c2ccccc2)ccc1)(=O)=O Chemical compound COc(c(OCc1ccccc1)cc1ncc2)cc1c2Oc(cc1F)ccc1NS(c1cc(-c2ccccc2)ccc1)(=O)=O DFLWWSFMWUEGDL-UHFFFAOYSA-N 0.000 description 1
- CIUKUFCCMMIELV-UHFFFAOYSA-N COc(cc1)c(cccc2)c2c1S(Nc(ccc(Oc1c(cc(c(OC)c2)OC)c2ncc1)c1)c1F)(=O)=O Chemical compound COc(cc1)c(cccc2)c2c1S(Nc(ccc(Oc1c(cc(c(OC)c2)OC)c2ncc1)c1)c1F)(=O)=O CIUKUFCCMMIELV-UHFFFAOYSA-N 0.000 description 1
- FRCCFKSQPXBZTN-UHFFFAOYSA-N COc(cccc1)c1S(Nc(c(F)c1)ccc1Oc1c(cc(c(OC)c2)OC)c2ncc1)(=O)=O Chemical compound COc(cccc1)c1S(Nc(c(F)c1)ccc1Oc1c(cc(c(OC)c2)OC)c2ncc1)(=O)=O FRCCFKSQPXBZTN-UHFFFAOYSA-N 0.000 description 1
- RZMYGXRQDHVUKV-UHFFFAOYSA-N C[n]1cnc(S(NC(C(C2)F)=CC=C2Oc(c2c3)cc[n]c2cc(OC)c3OC)(=O)=O)c1 Chemical compound C[n]1cnc(S(NC(C(C2)F)=CC=C2Oc(c2c3)cc[n]c2cc(OC)c3OC)(=O)=O)c1 RZMYGXRQDHVUKV-UHFFFAOYSA-N 0.000 description 1
- BKQLUCYOMCCYQG-UHFFFAOYSA-N Cc([nH]1)ncc1S(Nc(cc1)cc(F)c1OC1c(cccc2C(F)(F)F)c2N=C(C)C1)(=O)=O Chemical compound Cc([nH]1)ncc1S(Nc(cc1)cc(F)c1OC1c(cccc2C(F)(F)F)c2N=C(C)C1)(=O)=O BKQLUCYOMCCYQG-UHFFFAOYSA-N 0.000 description 1
- UPDPHLWJXBYILK-UHFFFAOYSA-N Cc([nH]1)ncc1S(Nc(cc1)ccc1Oc1c(cc(c(OC)c2)OC)c2ncc1)(=O)=O Chemical compound Cc([nH]1)ncc1S(Nc(cc1)ccc1Oc1c(cc(c(OC)c2)OC)c2ncc1)(=O)=O UPDPHLWJXBYILK-UHFFFAOYSA-N 0.000 description 1
- FPRHOANXSWALTR-UHFFFAOYSA-N Cc(c(OC)cc1ncc2)cc1c2Oc(cc1)cc(F)c1NS(c1cccc(F)c1)(=O)=O Chemical compound Cc(c(OC)cc1ncc2)cc1c2Oc(cc1)cc(F)c1NS(c1cccc(F)c1)(=O)=O FPRHOANXSWALTR-UHFFFAOYSA-N 0.000 description 1
- TZIROANCUUDQMF-UHFFFAOYSA-N Cc(cc(cc1)NS(C)(c2ccccc2C(F)(F)F)(O)=O)c1OC1c(cc(c(OC)c2)OC)c2N=CC1 Chemical compound Cc(cc(cc1)NS(C)(c2ccccc2C(F)(F)F)(O)=O)c1OC1c(cc(c(OC)c2)OC)c2N=CC1 TZIROANCUUDQMF-UHFFFAOYSA-N 0.000 description 1
- SVYFSMVDGXXEOX-UHFFFAOYSA-N Cc(cc(cc1)NS(c2cc(-c3ncccn3)ccc2)(=O)=O)c1Oc1c(cc(c(OC)c2)OC)c2ncc1 Chemical compound Cc(cc(cc1)NS(c2cc(-c3ncccn3)ccc2)(=O)=O)c1Oc1c(cc(c(OC)c2)OC)c2ncc1 SVYFSMVDGXXEOX-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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 ring carbon atoms
- C07D215/20—Oxygen atoms
-
- 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
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms 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
- C07D413/12—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)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4539808P | 2008-04-16 | 2008-04-16 | |
| US61/045,398 | 2008-04-16 | ||
| PCT/EP2009/002798 WO2009127417A1 (en) | 2008-04-16 | 2009-04-16 | Quinoline derivatives as axl kinase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011517689A JP2011517689A (ja) | 2011-06-16 |
| JP2011517689A5 JP2011517689A5 (enExample) | 2012-05-31 |
| JP5746015B2 true JP5746015B2 (ja) | 2015-07-08 |
Family
ID=40999731
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011504377A Active JP5746015B2 (ja) | 2008-04-16 | 2009-04-16 | Axlキナーゼ阻害剤としてのキノリン誘導体 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US9206130B2 (enExample) |
| EP (1) | EP2262772B8 (enExample) |
| JP (1) | JP5746015B2 (enExample) |
| KR (1) | KR101325237B1 (enExample) |
| CN (1) | CN102131783A (enExample) |
| AU (1) | AU2009237938A1 (enExample) |
| CA (1) | CA2718538A1 (enExample) |
| ES (1) | ES2391373T3 (enExample) |
| IL (1) | IL208103A (enExample) |
| MX (1) | MX2010011224A (enExample) |
| RU (1) | RU2010146474A (enExample) |
| WO (1) | WO2009127417A1 (enExample) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2311809A1 (en) * | 2009-10-16 | 2011-04-20 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Quinolinyloxyphenylsulfonamides |
| EP2423208A1 (en) * | 2010-08-28 | 2012-02-29 | Lead Discovery Center GmbH | Pharmaceutically active compounds as Axl inhibitors |
| ITRM20100537A1 (it) | 2010-10-12 | 2012-04-12 | Consiglio Nazionale Ricerche | Aptamero inibitore del recettore tirosina chinasi axl per uso in terapia |
| EP3045453A1 (en) * | 2011-11-14 | 2016-07-20 | Cephalon, Inc. | Uracil derivatives as axl and c-met kinase inhibitors |
| DK2810937T3 (en) | 2012-01-31 | 2017-03-13 | Daiichi Sankyo Co Ltd | PYRIDONE DERIVATIVES |
| US20150164800A1 (en) | 2012-07-25 | 2015-06-18 | Xetrios Therapeutics, Inc. | Regulating the interaction between tam ligands and lipid membranes with exposed phosphatidyl serine |
| TWI649308B (zh) | 2013-07-24 | 2019-02-01 | 小野藥品工業股份有限公司 | 喹啉衍生物 |
| US9771333B2 (en) | 2013-11-20 | 2017-09-26 | Signalchem Lifesciences Corp. | Quinazoline derivatives as TAM family kinase inhibitors |
| US9873670B2 (en) | 2013-11-22 | 2018-01-23 | University Of Kentucky Research Foundation | Arylquinoline and analog compounds and use thereof to treat cancer |
| EP3074390B1 (en) | 2013-11-27 | 2020-07-08 | SignalChem Lifesciences Corporation | Aminopyridine derivatives as tam family kinase inhibitors |
| TWI723572B (zh) | 2014-07-07 | 2021-04-01 | 日商第一三共股份有限公司 | 具有四氫吡喃基甲基之吡啶酮衍生物及其用途 |
| ES2749726T3 (es) * | 2014-12-25 | 2020-03-23 | Ono Pharmaceutical Co | Derivado de quinolina |
| WO2016183071A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Hetero-tricyclic compounds and their use for the treatment of cancer |
| WO2017027717A1 (en) | 2015-08-12 | 2017-02-16 | Incyte Corporation | Bicyclic fused pyrimidine compounds as tam inhibitors |
| WO2017035366A1 (en) | 2015-08-26 | 2017-03-02 | Incyte Corporation | Pyrrolopyrimidine derivatives as tam inhibitors |
| ES2896079T3 (es) | 2016-02-26 | 2022-02-23 | Ono Pharmaceutical Co | Fármaco para la terapia del cáncer, caracterizado por la administración de la combinación entre un inhibidor de Axl y un inhibidor del punto de control inmunitario |
| JP7034084B2 (ja) | 2016-03-28 | 2022-03-11 | インサイト・コーポレイション | Tam阻害剤としてのピロロトリアジン化合物 |
| CN108250200A (zh) * | 2016-12-28 | 2018-07-06 | 中国科学院上海药物研究所 | 一种具有Axl抑制活性的化合物及其制备和应用 |
| HUE054883T2 (hu) | 2017-01-26 | 2021-10-28 | Ono Pharmaceutical Co | N-{5-[(6,7-dimetoxi-4-kinolinil)oxi]-2-piridinil}-2,5-dioxo-1-fenil-1,2,5,6,7,8-hexahidro-3-kinolinkarboxamid etánszulfonát sója |
| US20200197385A1 (en) | 2017-08-23 | 2020-06-25 | Ono Pharmaceutical Co., Ltd. | Therapeutic agent for cancer containing axl inhibitor as active ingredient |
| CA3074013A1 (en) * | 2017-08-31 | 2019-03-07 | Abbvie Inc. | Ectonucleotide pyrophosphatase-phosphodiesterase 1 (enpp-1) inhibitors and uses thereof |
| CA3077308A1 (en) | 2017-09-27 | 2019-04-04 | Incyte Corporation | Salts of pyrrolotriazine derivatives useful as tam inhibitors |
| WO2019074116A1 (ja) | 2017-10-13 | 2019-04-18 | 小野薬品工業株式会社 | Axl阻害剤を有効成分として含む固形がん治療剤 |
| EA202190153A1 (ru) | 2018-06-29 | 2021-04-09 | Инсайт Корпорейшн | Составы ингибитора axl/mer |
| KR20210142154A (ko) | 2019-03-21 | 2021-11-24 | 옹쎄오 | 암 치료를 위한 키나제 억제제와 조합된 dbait 분자 |
| JP2023500906A (ja) | 2019-11-08 | 2023-01-11 | インサーム(インスティテュ ナシオナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシェ メディカル) | キナーゼ阻害剤に対する獲得抵抗性を有するがんの処置方法 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| AU2021230385A1 (en) | 2020-03-06 | 2022-09-22 | Incyte Corporation | Combination therapy comprising AXL/MER and PD-1/PD-L1 inhibitors |
| CA3182673A1 (en) * | 2020-05-08 | 2021-11-11 | Georgiamune Llc | Akt3 modulators |
| JP2022104746A (ja) * | 2020-12-29 | 2022-07-11 | 国立研究開発法人国立がん研究センター | 抗がん剤 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
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| GB9510757D0 (en) * | 1994-09-19 | 1995-07-19 | Wellcome Found | Therapeuticaly active compounds |
| HU230789B1 (en) * | 1999-01-22 | 2018-05-02 | Kyowa Hakko Kirin Co | Quinoline derivatives and quinazoline derivatives, pharmaceutical compositions containing them and their use |
| US7041691B1 (en) * | 1999-06-30 | 2006-05-09 | Amgen Inc. | Compounds for the modulation of PPARγ activity |
| EP1566379A4 (en) * | 2002-10-29 | 2005-11-09 | Kirin Brewery | CHINOLINE DERIVATIVES AND CHINAZOLINE DERIVATIVES AS INHIBITORS OF FLT3 AUTOPHOSPHORYLATION AND THE MEDICAL COMPOSITIONS CONTAINING THEREOF |
| CA2744997A1 (en) * | 2003-09-26 | 2005-04-07 | Exelixis, Inc. | C-met modulators and method of use |
| GB0509227D0 (en) | 2005-05-05 | 2005-06-15 | Chroma Therapeutics Ltd | Intracellular enzyme inhibitors |
| EP1919900A2 (de) * | 2005-08-22 | 2008-05-14 | Boehringer Ingelheim International Gmbh | Bicyclische heterocyclen, diese verbindungen enthaltende arzneimittel, deren verwendung und verfahren zu ihrer herstellung |
| CN101528702A (zh) * | 2006-06-08 | 2009-09-09 | 阿雷生物药品公司 | 喹啉化合物和使用方法 |
| CN105106199A (zh) * | 2006-12-14 | 2015-12-02 | 埃克塞利希斯股份有限公司 | 使用mek抑制剂的方法 |
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- 2009-04-16 KR KR1020107023097A patent/KR101325237B1/ko active Active
- 2009-04-16 MX MX2010011224A patent/MX2010011224A/es not_active Application Discontinuation
- 2009-04-16 US US12/933,070 patent/US9206130B2/en active Active
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- 2009-04-16 CN CN2009801129869A patent/CN102131783A/zh active Pending
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Also Published As
| Publication number | Publication date |
|---|---|
| KR101325237B1 (ko) | 2013-11-04 |
| KR20100132038A (ko) | 2010-12-16 |
| WO2009127417A1 (en) | 2009-10-22 |
| ES2391373T3 (es) | 2012-11-23 |
| US20110092503A1 (en) | 2011-04-21 |
| EP2262772A1 (en) | 2010-12-22 |
| EP2262772B1 (en) | 2012-07-18 |
| EP2262772B8 (en) | 2013-03-13 |
| RU2010146474A (ru) | 2012-05-27 |
| IL208103A0 (en) | 2010-12-30 |
| AU2009237938A1 (en) | 2009-10-22 |
| JP2011517689A (ja) | 2011-06-16 |
| CA2718538A1 (en) | 2009-10-22 |
| MX2010011224A (es) | 2011-02-25 |
| IL208103A (en) | 2015-08-31 |
| US9206130B2 (en) | 2015-12-08 |
| CN102131783A (zh) | 2011-07-20 |
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