FIELD: pharmaceuticals.
SUBSTANCE: group of inventions relates to a new type of indoleheptamyloxime compounds as a PARP inhibitor. The following is disclosed: a compound of formula (II), a stereoisomer thereof, or a pharmaceutically acceptable salt thereof,
,
where selected from the group consisting of a single bond and a double bond; X is selected from the group consisting of CR 3 and N; Y is selected from the group consisting of CR1 and C; L1 is selected from the group consisting of a single bond and -(CR8R9)n; L2 is selected from the group consisting of a single bond, -CR8R9- and =CH-; L1 and L2 do not represent single bonds at the same time; if L2 is selected from a single bond, then selected from a single bond; each of L3 and L4 is independently selected from -CR8R9-; n is either 1 or 2; R1 is selected from the group consisting of H, D, F, Cl, Br, I and C1-3 alkyl, and if L2 is selected from =CH-, then R1 is absent; each of R2 and R10 is independently selected from the group consisting of H, F, Cl, Br and I; R3 is selected from the group consisting of H, F, Cl, Br and I; R4 is selected from the group consisting of H and F; R5 is selected from the group consisting of H and C1-3 alkyl; each of R6 and R7 is independently selected from the group consisting of H and D; each of R8 and R9 is H. Also the following is disclosed: compounds falling under formula (II), a pharmaceutical composition containing a compound of formula (II), a method of treating a PARP receptor-associated disease using a compound of formula (II), and the use of compounds of formula (II) for the treatment of a disease associated with the PARP receptor.
EFFECT: provision of indolheptamyloxime compounds as a PARP inhibitor.
24 cl, 10 tbl, 89 ex
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Authors
Dates
2024-01-10—Published
2020-02-03—Filed