FIELD: biochemistry.
SUBSTANCE: invention relates to compounds of Formula I, their deuterated derivatives and pharmaceutically acceptable salts, while in the Formula R1 represents a hydrogen atom or C1-C6 alkyl; R2 and R3 represent C1-C6 alkyl or R2 and R3 together with C atom to which they are attached form C3-C6 cycloalkyl; R4 and R5 are independently selected from hydrogen and halogen, and at least one of R4 and R5 represent halogen; R6 selected from a hydrogen atom or C1-C6 alkyl; R7 represents , Z is O or , and n is an integer from 0 to 4; each of W and Y is independently C or N, but both W and Y cannot be C at the same time, and if Z is O, W is C; R10, R11, R12 and R13 are independently selected from a hydrogen atom, C1-C6 alkyl, C1-C6 hydroxyalkyl or cyclopropylmethyl, or R6 and R7 together with the C atoms to which they are attached form a 6-membered heterocycle containing one N atom, which is substituted by ; R8 represents C1-C6 hydroxyalkyl. The invention also relates to intermediates of Formula VI, a method for the preparation and use of compounds of Formula I, a pharmaceutical composition, a kit and methods of treatment.
EFFECT: compounds of Formula I are obtained with inhibitory activity against CDK 4/6.
29 cl, 12 tbl, 52 ex
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Authors
Dates
2021-06-10—Published
2016-11-28—Filed