FIELD: chemistry.
SUBSTANCE: present invention relates to a novel compound of formula:
or to its pharmacologically acceptable salt. In said structural formulas A is selected from: partially saturated or unsaturated 5- or 6-member heterocyclyl selected from pyrrolyl, pyrazolyl, imidazolyl, triazolyl, imidazolidinyl, pyrrolidinyl, pyrrolidinylidene, dihydropyrrolyl, isoxazolyl-dihydrooxazolyl, isoxazolidinyl, oxazolidinyl and oxazolyl, where said partially saturated or unsaturated 5- or 6-member heterocyclyl is optionally substituted with one or more oxo, C1-6alkyl, amino, hydroxyl or halogen; C1-6alkoxylamine; C1-6alkylamine, optionally substituted with one or more substitutes, which are C1-6alkyl, C1-6haloalkyl, hydroxyl or halogen; C0-6alkyl-carboxylic acid; C1-6alkylhydroxyl; saturated or unsaturated C0-6alkyl-bicyclic-heterocyclyl, selected from indolyl, isoindolyl, indolinyl and isoindolinyl, where said saturated or unsaturated C0-6alkyl-bicyclic-heterocyclyl is optionally substituted with one or more oxo; and saturated or unsaturated C1-6alkoxy-bicyclic-heterocyclyl, selected from indolyl, isoindolyl, indolinyl and isoindolinyl, where said C1-6alkoxy-bicyclic-heterocyclyl is optionally substituted with one or more oxo.
EFFECT: compound is used for preventive or therapeutic treatment of fibrosis.
27 cl, 22 dwg, 15 ex
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Authors
Dates
2020-01-24—Published
2016-03-18—Filed