EA201492092A1 - Соединения и композиции для ингибирования активности abl1, abl2 и bcr-abl1 - Google Patents
Соединения и композиции для ингибирования активности abl1, abl2 и bcr-abl1Info
- Publication number
- EA201492092A1 EA201492092A1 EA201492092A EA201492092A EA201492092A1 EA 201492092 A1 EA201492092 A1 EA 201492092A1 EA 201492092 A EA201492092 A EA 201492092A EA 201492092 A EA201492092 A EA 201492092A EA 201492092 A1 EA201492092 A1 EA 201492092A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- abl1
- compounds
- bcr
- inhibiting
- activity
- Prior art date
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Classifications
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- 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
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/357—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having two or more oxygen atoms in the same ring, e.g. crown ethers, guanadrel
- A61K31/36—Compounds containing methylenedioxyphenyl groups, e.g. sesamin
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- A61K31/33—Heterocyclic compounds
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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- 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
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- A61K31/425—Thiazoles
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
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- 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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- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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Abstract
Изобретение относится к соединениям формулы (I)в которой Y, Y, Y, Y, Y, R, R, Rи Rимеют значения, как описано в описании изобретения, способным ингибировать активность BCR-ABL1 и его мутаций. Данное изобретение далее относится к способу получения соединений согласно данному изобретению, фармацевтическим готовым лекарственным формам, содержащим такие соединения, и к способам применения таких соединений при лечении раковых заболеваний.
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PCT/IB2013/053770 WO2013171641A1 (en) | 2012-05-15 | 2013-05-09 | Compounds and compositions for inhibiting the activity of abl1, abl2 and bcr-abl1 |
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WO2013171641A1 (en) | 2013-11-21 |
US9315489B2 (en) | 2016-04-19 |
BR112014027584A2 (pt) | 2017-06-27 |
CN104334529B (zh) | 2017-03-15 |
CN104334529A (zh) | 2015-02-04 |
KR20150014452A (ko) | 2015-02-06 |
EP2900637A1 (en) | 2015-08-05 |
US20160185733A1 (en) | 2016-06-30 |
EA026559B1 (ru) | 2017-04-28 |
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