FIELD: chemistry.
SUBSTANCE: invention relates to organic chemistry and specifically to a heterocyclic compound of formula (I) and a pharmaceutically acceptable salt thereof, where R1 is H; R2 is -(C1alkyl)nN (R9)2; R3 and R5 are H; R4 is -phenyl (R13)q; each R9 is independently selected from a group consisting of H, -C1-3alkyl, -(C1-3alkyl)ncyclopentyl and -(C1-2alkyl)N(R16)2; alternatively, two adjacent R9 can together with atoms, to which they are bonded, form heterocyclyl(R17)q, where heterocyclyl is selected from piperazine, pyrrolidine and piperidine; each R13 is a substituent attached to an aryl ring and is independently selected from a group consisting of halogenide, -morpholinyl, -N(R9)2 and -(C1alkyl)nNHSO2R18; each R16, R17 and R18 are methyl; A is C; each q is integer from 1 to 2; and each n is integer of 0 or 1. Invention also relates to a heterocyclic compound of formula (II), values of radicals are given in patent claim, pharmaceutical composition based on compound of formula (I) or (II), a method of treating said diseases and a method of inhibiting one or more Wnt proteins.
I II.
EFFECT: obtaining novel heterocyclic compounds which are useful in treating Wnt mediated diseases.
40 cl, 6 tbl, 10 ex
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Authors
Dates
2019-05-24—Published
2013-05-03—Filed