JP6093768B2 - 特定の化学的実体、組成物、および方法 - Google Patents
特定の化学的実体、組成物、および方法 Download PDFInfo
- Publication number
- JP6093768B2 JP6093768B2 JP2014530915A JP2014530915A JP6093768B2 JP 6093768 B2 JP6093768 B2 JP 6093768B2 JP 2014530915 A JP2014530915 A JP 2014530915A JP 2014530915 A JP2014530915 A JP 2014530915A JP 6093768 B2 JP6093768 B2 JP 6093768B2
- Authority
- JP
- Japan
- Prior art keywords
- carbonyl
- phenyl
- quinoxaline
- urea
- fluoro
- 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.)
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Links
- WOMFDOGSSUTJCT-UHFFFAOYSA-N CC(C)(C)C(Nc(cc(c(F)c1)F)c1F)=O Chemical compound CC(C)(C)C(Nc(cc(c(F)c1)F)c1F)=O WOMFDOGSSUTJCT-UHFFFAOYSA-N 0.000 description 1
- MUQBJUDJUAEDFJ-UHFFFAOYSA-N CC(C)(C)C(Nc(cc(c(F)c1C(c(cc2)cc3c2ncc(N2CCOCC2)n3)O)F)c1F)=O Chemical compound CC(C)(C)C(Nc(cc(c(F)c1C(c(cc2)cc3c2ncc(N2CCOCC2)n3)O)F)c1F)=O MUQBJUDJUAEDFJ-UHFFFAOYSA-N 0.000 description 1
- KCSWZBNUOZSBHF-UHFFFAOYSA-N CC(C)(C)C(Nc(cc1)cc(C(c(cc2)cc3c2ncc(O)n3)=O)c1F)=O Chemical compound CC(C)(C)C(Nc(cc1)cc(C(c(cc2)cc3c2ncc(O)n3)=O)c1F)=O KCSWZBNUOZSBHF-UHFFFAOYSA-N 0.000 description 1
- WCWGASQVFBSFIN-UHFFFAOYSA-N CC(C)(C)C(Nc(cc1C(c(cc2)cc3c2ncc(OC)n3)=O)ccc1F)=O Chemical compound CC(C)(C)C(Nc(cc1C(c(cc2)cc3c2ncc(OC)n3)=O)ccc1F)=O WCWGASQVFBSFIN-UHFFFAOYSA-N 0.000 description 1
- LIJYXDKEMCTTAV-UHFFFAOYSA-N CC(C)(C)C(Nc1cccc(Br)c1)=O Chemical compound CC(C)(C)C(Nc1cccc(Br)c1)=O LIJYXDKEMCTTAV-UHFFFAOYSA-N 0.000 description 1
- MIEFENTVZPQCLK-UHFFFAOYSA-N CC(C)(C)C(Nc1cccc(C(c(cc2)cc3c2ncc(Cl)n3)O)c1)=O Chemical compound CC(C)(C)C(Nc1cccc(C(c(cc2)cc3c2ncc(Cl)n3)O)c1)=O MIEFENTVZPQCLK-UHFFFAOYSA-N 0.000 description 1
- IBTWEHVRTMVTGB-UHFFFAOYSA-N CCOC(c(cc1)cc2c1ncc(OC)n2)=O Chemical compound CCOC(c(cc1)cc2c1ncc(OC)n2)=O IBTWEHVRTMVTGB-UHFFFAOYSA-N 0.000 description 1
- YZYIGFRJTNPGRN-UHFFFAOYSA-N COc1nc(cc(cc2)C(O)=O)c2nc1 Chemical compound COc1nc(cc(cc2)C(O)=O)c2nc1 YZYIGFRJTNPGRN-UHFFFAOYSA-N 0.000 description 1
- JYNKGURHTLESKY-UHFFFAOYSA-N O=C(C(C1)C(F)=CC=C1NC(c1cccc(F)c1)=O)c(cc1)cc2c1ncc(N1CCOCC1)n2 Chemical compound O=C(C(C1)C(F)=CC=C1NC(c1cccc(F)c1)=O)c(cc1)cc2c1ncc(N1CCOCC1)n2 JYNKGURHTLESKY-UHFFFAOYSA-N 0.000 description 1
- YNSAPZBQJCGSNY-UHFFFAOYSA-N O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c(cc(cc1)NC(Nc(cc2)ccc2Cl)=O)c1F Chemical compound O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c(cc(cc1)NC(Nc(cc2)ccc2Cl)=O)c1F YNSAPZBQJCGSNY-UHFFFAOYSA-N 0.000 description 1
- LNMBHUZVBWDOJY-UHFFFAOYSA-N O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c(cc(cc1)NC(Nc2cccc(Cl)c2)=O)c1F Chemical compound O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c(cc(cc1)NC(Nc2cccc(Cl)c2)=O)c1F LNMBHUZVBWDOJY-UHFFFAOYSA-N 0.000 description 1
- MCSBITWDDZLSKL-UHFFFAOYSA-N O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c(cc(cc1)NC(Nc2cccc(F)c2)=O)c1F Chemical compound O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c(cc(cc1)NC(Nc2cccc(F)c2)=O)c1F MCSBITWDDZLSKL-UHFFFAOYSA-N 0.000 description 1
- XRCVVTLVQJEOJS-UHFFFAOYSA-N O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c(cc(cc1)NC(Nc2cncc(Cl)c2)=O)c1F Chemical compound O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c(cc(cc1)NC(Nc2cncc(Cl)c2)=O)c1F XRCVVTLVQJEOJS-UHFFFAOYSA-N 0.000 description 1
- DLHBGHZIEVWIOH-UHFFFAOYSA-N O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c(cc(cc1F)NC(Nc2cccc(F)c2)=O)c1F Chemical compound O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c(cc(cc1F)NC(Nc2cccc(F)c2)=O)c1F DLHBGHZIEVWIOH-UHFFFAOYSA-N 0.000 description 1
- NKGYESYUDKXMGA-UHFFFAOYSA-N O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c1cc(F)cc(NC(Nc(cc2)cc(F)c2F)=O)c1 Chemical compound O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c1cc(F)cc(NC(Nc(cc2)cc(F)c2F)=O)c1 NKGYESYUDKXMGA-UHFFFAOYSA-N 0.000 description 1
- YWXRZTFDYKPDAE-UHFFFAOYSA-N O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c1cc(F)cc(NC(c(cc2C(F)(F)F)ccc2Cl)=O)c1 Chemical compound O=C(c(cc1)cc2c1ncc(N1CCOCC1)n2)c1cc(F)cc(NC(c(cc2C(F)(F)F)ccc2Cl)=O)c1 YWXRZTFDYKPDAE-UHFFFAOYSA-N 0.000 description 1
- XADWMDLROUXERU-UHFFFAOYSA-N O=C(c(cc1)cc2c1nccn2)c(c(F)c(cc1)NC(Nc2cccc(F)c2)=O)c1F Chemical compound O=C(c(cc1)cc2c1nccn2)c(c(F)c(cc1)NC(Nc2cccc(F)c2)=O)c1F XADWMDLROUXERU-UHFFFAOYSA-N 0.000 description 1
- ALWINVOIYBNECK-UHFFFAOYSA-N O=C(c(cc1)cc2c1nccn2)c(cc(cc1F)NC(Nc(cc2C(F)(F)F)ccc2Cl)=O)c1F Chemical compound O=C(c(cc1)cc2c1nccn2)c(cc(cc1F)NC(Nc(cc2C(F)(F)F)ccc2Cl)=O)c1F ALWINVOIYBNECK-UHFFFAOYSA-N 0.000 description 1
- HDWVUWSNLBZWPB-UHFFFAOYSA-N O=C(c(cc1)cc2c1nccn2)c(cc(cc1F)NC(Nc2cccc(C(F)(F)F)c2)=O)c1F Chemical compound O=C(c(cc1)cc2c1nccn2)c(cc(cc1F)NC(Nc2cccc(C(F)(F)F)c2)=O)c1F HDWVUWSNLBZWPB-UHFFFAOYSA-N 0.000 description 1
- DWSXTXRPXOHHIM-UHFFFAOYSA-N O=C(c(cc1)cc2c1nccn2)c1cc(F)cc(NC(Nc(cc2)ccc2Cl)=O)c1 Chemical compound O=C(c(cc1)cc2c1nccn2)c1cc(F)cc(NC(Nc(cc2)ccc2Cl)=O)c1 DWSXTXRPXOHHIM-UHFFFAOYSA-N 0.000 description 1
- JPHQBYZNVFHQJL-UHFFFAOYSA-N O=C(c(cc1)cc2c1nccn2)c1cc(F)cc(NC(Nc(cc2Cl)ccc2F)=O)c1 Chemical compound O=C(c(cc1)cc2c1nccn2)c1cc(F)cc(NC(Nc(cc2Cl)ccc2F)=O)c1 JPHQBYZNVFHQJL-UHFFFAOYSA-N 0.000 description 1
- MCWYGVRYGOFQTA-UHFFFAOYSA-N O=C(c(cc1)cc2c1nccn2)c1cc(F)cc(NC(Nc(cc2F)ccc2F)=O)c1 Chemical compound O=C(c(cc1)cc2c1nccn2)c1cc(F)cc(NC(Nc(cc2F)ccc2F)=O)c1 MCWYGVRYGOFQTA-UHFFFAOYSA-N 0.000 description 1
- CBBQZDKNHLHXCD-UHFFFAOYSA-N O=C(c(cc1)cc2c1nccn2)c1cc(F)cc(NC(Nc2ccc(C(F)(F)F)cc2)=O)c1 Chemical compound O=C(c(cc1)cc2c1nccn2)c1cc(F)cc(NC(Nc2ccc(C(F)(F)F)cc2)=O)c1 CBBQZDKNHLHXCD-UHFFFAOYSA-N 0.000 description 1
- OLVZQUYXZNQCGA-UHFFFAOYSA-N O=C(c1cc(NC(c(cc(C(F)(F)F)cc2)c2Cl)=O)ccc1)c(cc1)cc2c1nccn2 Chemical compound O=C(c1cc(NC(c(cc(C(F)(F)F)cc2)c2Cl)=O)ccc1)c(cc1)cc2c1nccn2 OLVZQUYXZNQCGA-UHFFFAOYSA-N 0.000 description 1
- NIJKHYHHRKWAKS-UHFFFAOYSA-N O=C(c1cccc(NC(c2cccc(F)c2)=O)c1)c(cc1)cc2c1ncc(N1CCOCC1)n2 Chemical compound O=C(c1cccc(NC(c2cccc(F)c2)=O)c1)c(cc1)cc2c1ncc(N1CCOCC1)n2 NIJKHYHHRKWAKS-UHFFFAOYSA-N 0.000 description 1
- MHFXHWJNDUUNPP-UHFFFAOYSA-N O=Cc(cc1)cc2c1ncc(Cl)n2 Chemical compound O=Cc(cc1)cc2c1ncc(Cl)n2 MHFXHWJNDUUNPP-UHFFFAOYSA-N 0.000 description 1
- JDFDKEUKGJPEHK-UHFFFAOYSA-N O=Cc(cc1)cc2c1ncc(N1CCOCC1)n2 Chemical compound O=Cc(cc1)cc2c1ncc(N1CCOCC1)n2 JDFDKEUKGJPEHK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
- C07D241/40—Benzopyrazines
- C07D241/42—Benzopyrazines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/495—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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
- C07D241/40—Benzopyrazines
- C07D241/44—Benzopyrazines 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 hetero ring
-
- 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
- C07D401/12—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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161534390P | 2011-09-14 | 2011-09-14 | |
| US61/534,390 | 2011-09-14 | ||
| US201161535992P | 2011-09-18 | 2011-09-18 | |
| US61/535,992 | 2011-09-18 | ||
| PCT/US2012/055653 WO2013040515A1 (en) | 2011-09-14 | 2012-09-14 | Certain chemical entities, compositions, and methods |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017024144A Division JP2017082011A (ja) | 2011-09-14 | 2017-02-13 | 特定の化学的実体、組成物、および方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014530194A JP2014530194A (ja) | 2014-11-17 |
| JP2014530194A5 JP2014530194A5 (https=) | 2015-11-05 |
| JP6093768B2 true JP6093768B2 (ja) | 2017-03-08 |
Family
ID=47883812
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014530915A Active JP6093768B2 (ja) | 2011-09-14 | 2012-09-14 | 特定の化学的実体、組成物、および方法 |
| JP2017024144A Withdrawn JP2017082011A (ja) | 2011-09-14 | 2017-02-13 | 特定の化学的実体、組成物、および方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017024144A Withdrawn JP2017082011A (ja) | 2011-09-14 | 2017-02-13 | 特定の化学的実体、組成物、および方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (6) | US9518029B2 (https=) |
| EP (2) | EP3332785B1 (https=) |
| JP (2) | JP6093768B2 (https=) |
| CN (3) | CN115403531A (https=) |
| AU (2) | AU2012308238B2 (https=) |
| CA (1) | CA2848506C (https=) |
| WO (1) | WO2013040515A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2017082011A (ja) * | 2011-09-14 | 2017-05-18 | ニューファーマ, インコーポレイテッド | 特定の化学的実体、組成物、および方法 |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201007286D0 (en) | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
| GB201020179D0 (en) | 2010-11-29 | 2011-01-12 | Astex Therapeutics Ltd | New compounds |
| ES2725790T3 (es) | 2011-08-26 | 2019-09-27 | Neupharma Inc | Algunas entidades químicas, composiciones, y métodos |
| US9249110B2 (en) | 2011-09-21 | 2016-02-02 | Neupharma, Inc. | Substituted quinoxalines as B-raf kinase inhibitors |
| US9249111B2 (en) | 2011-09-30 | 2016-02-02 | Neupharma, Inc. | Substituted quinoxalines as B-RAF kinase inhibitors |
| GB201118654D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
| GB201118656D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
| GB201118675D0 (en) | 2011-10-28 | 2011-12-14 | Astex Therapeutics Ltd | New compounds |
| GB201118652D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
| EP2806874B1 (en) | 2012-01-25 | 2017-11-15 | Neupharma, Inc. | Quinoxaline-oxy-phenyl derivatives as kinase inhibitors |
| MX371331B (es) | 2012-04-24 | 2020-01-27 | Vertex Pharma | Inhibidores de la proteina cinasa dependiente de acido desoxirribonucleico(adn-pk). |
| GB201209609D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
| GB201209613D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
| US9688635B2 (en) | 2012-09-24 | 2017-06-27 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| WO2014075077A1 (en) * | 2012-11-12 | 2014-05-15 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| ME03336B (me) | 2013-03-12 | 2019-10-20 | Vertex Pharma | Inhibitori dnk-pk |
| GB201307577D0 (en) | 2013-04-26 | 2013-06-12 | Astex Therapeutics Ltd | New compounds |
| BR112016005199B1 (pt) | 2013-08-23 | 2022-02-22 | Neupharma, Inc | Certos compostos químicos, composições, e métodos |
| JP6408569B2 (ja) | 2013-10-17 | 2018-10-17 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Dna−pk阻害剤としての(s)−n−メチル−8−(1−((2’−メチル−[4,5’−ビピリミジン]−6−イル)アミノ)プロパン−2−イル)キノリン−4−カルボキサミドおよびその重水素化誘導体の共結晶 |
| HRP20210319T1 (hr) | 2014-03-26 | 2021-04-30 | Astex Therapeutics Ltd. | Kombinacije inhibitora fgfr i inhibitora igf1r |
| JO3512B1 (ar) | 2014-03-26 | 2020-07-05 | Astex Therapeutics Ltd | مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز |
| RU2715236C2 (ru) | 2014-03-26 | 2020-02-26 | Астекс Терапьютикс Лтд | Комбинации |
| TWI719960B (zh) | 2015-02-10 | 2021-03-01 | 英商阿斯迪克治療公司 | 新穎組成物 |
| US10478494B2 (en) | 2015-04-03 | 2019-11-19 | Astex Therapeutics Ltd | FGFR/PD-1 combination therapy for the treatment of cancer |
| EP3353164B1 (en) | 2015-09-23 | 2021-11-03 | Janssen Pharmaceutica, N.V. | Bi-heteroaryl substituted 1,4-benzodiazepines and uses thereof for the treatment of cancer |
| US11155555B2 (en) | 2015-09-23 | 2021-10-26 | Janssen Pharmaceutica Nv | Compounds |
| WO2018035061A1 (en) | 2016-08-15 | 2018-02-22 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| EP3518931A4 (en) | 2016-09-27 | 2020-05-13 | Vertex Pharmaceuticals Incorporated | METHOD FOR TREATING CANCER WITH A COMBINATION OF DNA-DAMAGING SUBSTANCES AND DNA-PK INHIBITORS |
| EA202192575A1 (ru) | 2019-03-21 | 2022-01-14 | Онксео | Соединения dbait в сочетании с ингибиторами киназ для лечения рака |
| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
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| JP2017082011A (ja) * | 2011-09-14 | 2017-05-18 | ニューファーマ, インコーポレイテッド | 特定の化学的実体、組成物、および方法 |
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