FIELD: medicine; pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (I)
,
where R1 is substituted phenyl-C1-6 alkyl, substituted phenoxy-C1-6 alkyl, substituted phenyl-C2-6 alkenyl, substituted pyridinyl or substituted pyridinyl-C1-6 alkyl, where substituted phenyl-C1-6 alkyl, substituted phenoxy-C1-6 alkyl, substituted phenyl-C2-6 alkenyl, substituted pyridinyl and substituted pyridinyl-C1-6 alkyl are substituted with groups R3, R4 and R5, Y is -OC(O)- or -C(O)-, W is -C(O)-, R2 is substituted phenyl or substituted pyridinyl, where substituted phenyl and substituted pyridinyl are substituted groups R6, R7 and R8, R3 is halogen-C1-6 alkoxy, C1-6 alkylcarbonylamino or tetrahydropyranyl-C1-6 alkoxy, R4 is H, C1-6 alkyl or C3-8 cycloalkyl, R5 is H, R6 is aminosulphonyl, R7 is H or a halogen atom, R8 is H, R9 is C1-6 alkyl, C1-6 alkoxy or a halogen atom, m, n, p and q are equal to 1, or pharmaceutically acceptable salts thereof. What is also presented is a pharmaceutical composition, use of the compound and a method of treatment.
EFFECT: disclosed compounds have inhibitory activity on the autotoxin and carbonic anhydrase II and can be used for treating or preventing ocular pathological conditions.
17 cl, 7 ex
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Authors
Dates
2020-06-30—Published
2016-09-20—Filed