FIELD: pharmaceutics.
SUBSTANCE: present invention relates to a sulfonamide or sulfinamide compound or a pharmaceutically acceptable salt thereof, which has an effect inducing BRD4 protein degradation in cancer cells, and to its use as an anticancer drug. Disclosed is a compound of formula (I) or a pharmaceutically acceptable salt thereof, where A and Q each independently represent a ring selected from phenyl; 5–6-membered aromatic heterocycle containing 1 nitrogen atom; ring is optionally substituted with a group selected from a halogen atom and a cyano group; Z1 is C, Z2 is C, Z3 is a group =CRZ3-, Z4 is a group =CRZ4-, Z5 is a group =CRZ5-, RZ3, RZ4, and RZ5 each independently represents a group selected from a hydrogen atom; halogen atom; hydroxyl group; cyano group; a C1–6alkyl group optionally substituted with a group selected from a halogen atom, a hydroxyl group, and C1–6alkoxy group; C3–10cycloalkyl group; and C1–6alkoxy group; substructures ,
are presented in the claim of the present invention. L, T and M are presented in the formula of the present invention, G is N, J is N, n is 1 or 2; R5 is a hydrogen atom; R6a and R6b each independently represent a group selected from a hydrogen atom, a halogen atom; and a cyano group; R7a and R7b each independently represent a hydrogen atom or a C1–6alkyl group optionally substituted with a hydroxyl group, or R7c represents a hydrogen atom, R7r is a C2–6alkylene group, R8a and R8b each independently represent a group selected from a hydrogen atom, a halogen atom; and C1–6alkoxy group; R9a and R9b each independently represent a group selected from a hydrogen atom; a C1–6alkyl group, optionally substituted with a hydroxyl group, and C1–6alkoxy group; R10a and R10b each independently represent a substitute selected from a hydrogen atom, and a C1–6alkyl group, optionally substituted with a substitute selected from a cyano group; C1–6alkoxycarbonyl group; hydroxycarbonyl group and -CO-N(R7a)(R7b); and R11 is a C1–6alkyl group. Invention also relates to individual compounds, as well as a pharmaceutical composition based on said compounds and use thereof for treating cancer by BRD4 protein degradation.
EFFECT: obtaining alternative compounds inducing BRD4 protein degradation, which can be used in medicine as an anticancer drug.
24 cl, 2 dwg, 8 tbl, 150 ex
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Authors
Dates
2024-11-13—Published
2021-02-05—Filed