FIELD: pharmaceuticals.
SUBSTANCE: invention relates to imidazolonyl quinoline compounds applicable for inhibiting kinase activity. Disclosed is a compound of formula (IV), in which Het1 denotes pyrazolyl, which can be unsubstituted or mono-, di- or trisubstituted, independently from each other, by Hal or A; A in each case independently denotes a straight or branched alkyl containing 1, 2, 3, 4, 5 or 6 C atoms, where independently of each other, 1, 2, 3, 4 or 5 H atoms can be replaced by Hal; Hal is F, Cl, Br or I; HET is selected from 3-difluoromethoxy-5-fluoropyridin-4-yl, 3-fluoro-5-methoxypyridin-4-yl, 3-fluoro-5-fluoromethoxypyridin-4-yl, 3-fluoro-5-(trideuteromethoxy)pyridin- 4-yl, as well as its pharmaceutically acceptable salt, tautomer or stereoisomer. What is also presented is a pharmaceutical composition which inhibits the activity of ATM kinase, containing the disclosed compound.
EFFECT: technical result is provision of small molecules, which effectively and selectively inhibit, regulate and/or modulate signal transduction by means of ATM kinase.
4 cl, 4 tbl, 16 ex
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Authors
Dates
2021-02-17—Published
2016-03-31—Filed