FIELD: chemistry.
SUBSTANCE: invention relates to use of a compound of formula (I) or a pharmaceutically acceptable salt thereof, or any of stereoisomeric forms thereof, or mixtures thereof for treating pathological condition mediated by Rac1 cell proteins. In formula (I) R1 and R1' are independently selected from a group consisting of H and CF3 (provided that at least one of R1 and R1' is different from H); A is a carboxylic or heterocyclic ring system with one ring, where ring forming ring system, contains 5–7 members, where each member is independently selected from C, N and CH; or denotes an aromatic ring; wherein A substituted with one or more radicals selected from a group consisting of H, nitro, straight or branched (C1-C6)alkyl, halogen-(C1-C6)alkyl and -SO2NR3R4; where each R3 independently represents H or straight or branched (C1-C4)alkyl, each R4 independently represents H or straight or branched (C1-C6)alkyl. Invention also relates to a compound of formula (II), method for production thereof and pharmaceutical composition containing said compound. In formula (II) A is a carboxylic or heterocyclic ring system with one ring, where ring forming a ring system contains 5–7 members, where each member is independently selected from C, N and CH; or denotes an aromatic ring.
EFFECT: disclosed compounds can be used as agents for treating fast-growing and/or resistant tumours.
14 cl, 9 dwg, 3 tbl, 7 ex
(I) (II)
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Authors
Dates
2017-03-09—Published
2012-10-10—Filed