FIELD: chemistry.
SUBSTANCE: present invention relates to novel thienopyridinone-based compounds, specifically to a compound of formula (I), including any tautomeric and stereochemically isomeric form thereof, where each of A1, A2 and A3 is independently CH or N; C1 is hydrogen or C1-4 alkyl; C2 is hydrogen, C1-4alkyl, hydroxyl or C1-4 alkoxy group; Y is a direct bond; each Rb is independently hydrogen; D is 3–12 membered heterocyclyl containing at least one heteroatom selected from N or O, where said heterocyclyl is optionally substituted with 1–2 substitutes Rc; each Rc is independently C1-6alkyl; B is 3–12-membered carbocyclyl or 3–12-membered heterocyclyl containing at least one heteroatom selected from N or O; or its pharmaceutically acceptable salt, or its solvate. Invention also relates to a pharmaceutical formulation, to use of a compound of formula (I) for preparing a drug, to a method for preventing or treating a condition mediated by FGFR kinase.
EFFECT: obtaining compounds exhibiting FGFR kinase inhibitory activity, which can be used to prevent or treat a condition mediated by FGFR kinase.
32 cl, 2 tbl, 2 ex
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Authors
Dates
2024-09-30—Published
2019-12-25—Filed