FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (Ia) or a pharmaceutically acceptable salt thereof that can inhibit nicotinamide adenine dinucleotide phosphate oxidase 4 (Nox4). In formula (Ia) m is equal either to 0 or 1; n is an integer from 2 to 5; each R1 is independently selected from C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 alkoxy, hydroxy and halogen; or two R1 attached to adjacent phenyl ring atoms, together with the phenyl ring atoms to which they are attached, can form a 4–6-membered non-aromatic ring, optionally containing one oxygen atom and optionally substituted by one or more groups independently selected from C1-C3 alkyl and halogen; each R1a is independently selected from C1-C6 alkyl, hydroxy and halogen; R2 is selected from C1-C6 alkyl, halogen and hydroxy; R3, R4, R5 and R6 are independently selected from H and F; any alkyl is optionally substituted with one or more halogens; provided that the compound is not N-[2-(2-hydroxyphenyl)ethyl]-2,4,6-trimethylbenzene-1-sulfonamide, N-[2-(2-hydroxyphenyl)ethyl]-4-methoxy- 2,6-dimethylbenzenesulfonamide, 2,6-dichloro-N-[2-(2-fluorophenyl)ethyl]benzene-1-sulfonamide, 2,4,6-trimethyl-N-[2-(2-methylphenyl)ethyl] benzene-1-sulfonamide, N-[2-(2-fluorophenyl)ethyl]-2,4,6-trimethylbenzene-1-sulfonamide, N-[2-(2-hydroxyphenyl)ethyl]-2-methylbenzene-1- sulfonamide, 2,4-dichloro-N-[2-(2-fluorophenyl)ethyl]benzene-1-sulfonamide, 2-bromo-N-[2-(2-fluorophenyl)ethyl]benzene-1-sulfonamide, 2- chloro-N-[2-(2-fluorophenyl)ethyl]-6-methylbenzene-1-sulfonamide, N-[2-(2-fluorophenyl)ethyl]-2,5-dimethylbenzene-1-sulfonamide or N-[2 -(2-fluorophenyl)ethyl]-2,3,5,6-tetramethylbenzene-1-sulfonamide.
EFFECT: pharmaceutical composition comprising the said compound, its use in the manufacture of a medicinal product for treating a disease that benefits from inhibition of Nox4 activity, and a method for treating a disease that benefits from inhibition of Nox4 activity.
18 cl, 19 dwg, 7 tbl, 48 ex
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Authors
Dates
2023-12-06—Published
2019-05-09—Filed