FIELD: pharmaceutical chemistry.
SUBSTANCE: group of inventions includes a compound of formula (I), its pharmaceutically acceptable salts, an enantiomer, a stereoisomer, specific compounds and their pharmaceutically acceptable salts given in the claims, as well as a pharmaceutical composition. In the formula (I) R1 is -OR5; R5 is -C1-C6alkyl; R6 is phenyl optionally substituted with one or more R10; R10 is at each occurrence independently -C1-C6alkyl, halogen, -OC1-C6alkyl, or -OC3-C6cycloalkyl, where each alkyl or cycloalkyl is optionally substituted with one or more -R12; any two R10, if present on non-adjacent atoms, may be combined to form a bridged C3-C8cycloalkyl; or any two R10, if present on adjacent atoms, may be combined to form either C3-C8cycloalkyl or heterocyclyl or heteroaryl selected from dihydrofuranyl, furanyl, oxazolyl, methyloxazolyl, pyrrolyl, N-methylpyrrolyl and pyrazolyl, and R12 is at each occurrence independently either -C1-C6alkyl, -OH, or halo.
EFFECT: imidazo[4,5-f]quinolin-3-yl]cyclohexane-1-carboxylic acid derivatives having inhibitory activity against CREB-binding protein (CBP) and/or p300.
27 cl, 1 dwg, 5 ex
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Authors
Dates
2023-09-12—Published
2019-06-28—Filed