FIELD: chemistry.
SUBSTANCE: present invention relates to an isoquinolinone derivative of formula 1, a stereoisomer thereof or a pharmaceutically acceptable salt thereof.
formula 1, in which
L1 is -(CH2)3- or -(CH2)2C(=O)-; Y is 4-6-membered monocyclic or 8-membered bicyclic heterocycloalkylene containing one or two nitrogen atoms, or 6-membered monocyclic heterocycloalkenylene containing one nitrogen atom; L2 is a single bond, -NHCO-, -NR2-, -O- or straight or branched C1-4alkylene substituted with one or more substitutes selected from the group consisting of oxo and amino, R2 is hydrogen or methyl; and Z is C3-6cycloalkyl, heterocycloalkyl, which is tetrahydrofuranyl or pyrrolidinyl, phenyl or heteroaryl selected from pyridyl, pyrimidyl and thiazole; where each said cycloalkyl, heterocycloalkyl, phenyl and heteroaryl is independently unsubstituted or substituted with one or more substituents selected from the group consisting of -F, -Cl, cyano, nitro, methyl, unsubstituted or substituted with one or more fluorine, methoxy substituted with one or more fluorine, carboxy(-CO2H), methoxycarbonyl and methylcarbonylamino. Technical result is development of PARP-1 inhibitor.
EFFECT: disclosed compounds can be effectively used to prevent or treat diseases associated with PARP-1, in particular ophthalmic diseases or disorders.
10 cl, 1 dwg, 4 tbl, 277 ex
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Authors
Dates
2024-03-18—Published
2020-10-29—Filed