FIELD: medicine; pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof. In formula (I), R1 and R2 are both H or combined to form an oxo group (=O); R3 and R4, identical or different, in each case independently selected from the group consisting of H and (C1-C6)alkyl; R5 is selected from a group consisting of phenyl and heteroaryl with 5 ring atoms, in which one ring atom is a heteroatom S, where heteroaryl is substituted with one group selected from (C1-C6)hydroxyalkyl, dimethylaminomethyl, (4-methylpiperazin-1-yl) methyl; Z is absent or is NH; Cy is a mono- or bicyclic heteroaryl with 5–9 ring atoms, in which two or four ring atoms are a N heteroatom, where said heteroaryl is optionally substituted with two groups, selected independently from -CN, NR10R11, phenyl and heteroaryl, which is pyridinyl; where said phenyl and heteroaryl are additionally optionally and independently substituted with one or two groups, selected from halogen, -OH, -CN; and wherein said heteroaryl is further optionally substituted with group of 2,2,2-trifluoroethane-1-ol; where R10, R11 are selected from a group consisting of H. Invention also relates to pharmaceutical compositions.
EFFECT: obtaining novel compounds of formula (I), having inhibitory activity on phosphoinositide-3-kinase (PI3K), and which can be used as a drug for treating disorders caused by mechanisms of PI3K enzymes.
16 cl, 13 ex
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Authors
Dates
2020-05-29—Published
2016-04-14—Filed