FIELD: pharmaceutical chemistry.
SUBSTANCE: group of inventions includes compounds of formula (I) or (II), specific compounds indicated in the claims, or their pharmaceutically acceptable salts, stereoisomers, their use and a method of treatment and inhibition based on them. Where in formulas (I) or (II) A represents or -NR3R4; X is hydrogen or halogen; Y is C3-8cycloalkyl or C6-20aryl substituted with halogen; Z is either -O- or -S-; L is linear -(CH2)n-, n is an integer from 3 to 10, where, optionally, one or more of -CH2- is replaced by one or more -NR5-, -(CO)- and -CR5R6 - and/or optionally one or more of -CH2CH2- may be replaced by -CH=CH-; R1 is C1-6 alkoxy or -(CO)NR7R8; R2 is hydrogen, C1-8alkylsulfanyl or -(CO)R9; R3 and R4 are independently hydrogen or C3-8 cycloalkyl; R5 and R6 independently represent hydrogen, C1-8 alkyl or carboxyl; R7 and R8 are independently hydrogen; R9 is C1-4alkyl optionally substituted with one or more selected amino, hydroxyl, NHC(O)C1-4alkyl groups; phenyl, C1-4alkylene C3-12heteroaryl, wherein heteroaryl contains one N atom and is optionally substituted with C1-4alkyl, and C1-4alkylene is substituted with a group selected from amino and NHC(O)C1-4alkyl.
EFFECT: quinolinyl derivatives as VEGFR-2 and/or HDAC6 inhibitors.
16 cl, 3 tbl, 98 ex
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Authors
Dates
2023-09-06—Published
2020-03-30—Filed