FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof, where X represents C=O or a bond; R1 is selected from the group consisting of H, C1-C3alkyl, C1-C3alkoxyC1-C3alkyl, C3-C6cycloalkyl, C1-C3alkoxy, N,N-diC1-C3alkylamino and 1-pyrrolidinyl, with the proviso that when R1 is C1-C3alkoxy, N,N-diC1-C3alkylamino or 1-pyrrolidinyl, X is C=O; R2 represents a hydrogen atom; R3 is selected from the group consisting of A, phenyl and monocyclic heteroaryl, the said monocyclic heteroaryl is selected from the group consisting of pyridine, thiophene and pyrazole, and the said phenyl and the said heteroaryl are optionally substituted with one or two of R4, R5, R6 and R7; R4, R5, R6 and R7 are independently selected from the group consisting of halogen, C1-C6alkyl, C1-C3haloalkoxy and C1-C6haloalkyl; A represents R12 is selected from the group consisting of C1-C3alkoxyC1-C3alkyl, C3-C6cycloalkyl and C1-C3haloalkyl; Y is selected from the group consisting of CH2, NSO2R9, O and a bond. The invention also relates to a pharmaceutical composition for the inhibition of Vps34 based on these compounds.
EFFECT: obtaining new compounds and a pharmaceutical composition based on them which can be used in medicine in the treatment of cancer.
25 cl, 2 tbl, 72 ex
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Authors
Dates
2023-10-16—Published
2018-08-23—Filed