FIELD: organic chemistry; pharmacology.
SUBSTANCE: group of inventions relates to the field of organic chemistry and pharmacology, namely to compounds having the inhibitory activity of cyclin-dependent kinases (CDKs) and represented by the formula (XI), where R1 is H, F or Cl; R2 is H, C1-C5alkyl, C1-C5fluoroalkyl or C3-C8cycloalkyl, in which each specified C1-C5alkyl and C1-C5fluoroalkyl is optionally replaced by R20 and each specified C3-C8cycloalkyl is optionally substituted by R21; R4 is H, C1-C4alkyl or C1-C4fluoroalkyl, in which each specified C1-C4alkyl and C1-C4fluoroalkyl is optionally substituted by R20; or R2 can be taken together with R4 to form a 6-membered heterocyclic ring, optionally containing an additional heteroatom selected from NR24 and O as a member of the ring, and the ring is optionally replaced by R21; R6 is H, F or Cl; R7 and R8 are H; R9 is OH; each R20 is independently OH or NR22R23; each R21 is independently F, NR22R23 or C1-C4alkyl; each R22 and R23 is independently H, C1-C2alkyl or C1-C2fluoroalkyl; R24 is H or C1-C4alkyl. In addition, a pharmaceutical composition inhibiting the activity of cyclin-dependent kinases (CDKs) containing a therapeutically effective amount of the compound of formula (XI), as well as a method for treating breast cancer, including the introduction of a therapeutically effective amount of the compound presented to the object, is described.
EFFECT: presented group of inventions provides effective treatment of breast cancer.
14 cl, 6 tbl, 149 ex
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Authors
Dates
2021-12-21—Published
2019-04-22—Filed