FIELD: medicine.
SUBSTANCE: present invention relates to a compound of the general formula (I) or its pharmaceutically acceptable salt:
,
where X is CR1R2, a carbonyl group, or a group of the formula (Ia):
; R1 and R2, independently of each other, are a hydrogen atom, a halogen atom, a hydroxy group, a substituted hydroxy group, an optionally substituted C1-C6alkyl group, or an optionally substituted C1-C6alkoxy group, where the term “substituted” refers to the substitution with at least one substituent selected from a group consisting of a deuterium atom, a halogen atom, a hydroxy group and C1-C6alkoxy group; p and q, independently of each other, are integers from 0 to 3, provided that the sum of p and q is 2 or more. A pharmaceutical composition with inhibitory activity against VAP-1, the use of a compound of the general formula (I) to obtain a drug, a method for treating a disease that can be prevented, relieved and/or treated by inhibiting VAP-1 are also proposed.
EFFECT: obtaining new compounds that exhibit inhibitory activity against vascular adhesion protein-1 (VAP-1).
20 cl, 4 tbl, 73 ex
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Authors
Dates
2021-10-12—Published
2017-12-27—Filed