FIELD: chemistry.
SUBSTANCE: invention relates to organic chemistry and specifically to a heterocyclic compound of formula (A) or a pharmaceutically acceptable salt thereof, where X1 is CH or N; X2 is S; Z is -C(=O)NH-, -C(=O)O-; n ranges from 0 to 1; R1 is (C1-C6)alkyl, halogen or trifluoromethyl; R2 is (C1-C6)alkyl or trifluoromethyl; R3 is C6aryl, which can be unsubstituted or contain a substitute selected from a group consisting of: C1 alkoxy, which can be further substituted with halogen, halogen, oxy-C6 aryl substituted with halogen, C6 aryl substituted with halogen, morpholinyl, pyrrolidinyl, and di-C1-C6-alkylamino, wherein in case C6 aryl is substituted with morpholinyl, it can contain second substitute, which is halogen. Invention also relates to specific compounds, a pharmaceutical composition based on compound of formula (A) or specific compound, use thereof and a method of killing or inhibiting mycobacterium growth, based on using the compound of formula (A) or a specific compound.
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EFFECT: technical result is obtaining novel heterocyclic compounds useful for treating mycobacterial infections.
12 cl, 1 dwg, 3 tbl, 4 ex
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Authors
Dates
2019-08-01—Published
2013-07-18—Filed