FIELD: chemistry.
SUBSTANCE: invention relates to compounds of general formula (I) or (II), or a stereoisomer or enantiomer thereof, a pharmaceutically acceptable salt, wherein X is independently selected and is CH or N; Q is independently selected and is H, -C1-6-alkyl, phenyl, halogenated phenyl, naphthyl or halogenated naphthyl; R1, R2, R3, R4 are independently selected and are H, -C1-6-alkyl, -OH, halogen, -O-benzyl, phenyl, wherein the phenyl or benzyl can be optionally substituted with at least one substituent selected from halogen, -CN, -OH, -O-C1-6-alkyl, -COOH, -COOC1-6-alkyl, where R1 and R2 can form a bicyclic naphthyl moiety together with the cycle to which they are attached; R5, R6 are independently selected and are halogen.
formula (I),
formula (II).
EFFECT: according to the invention, the compounds are intended for treating and/or preventing an infectious disease of microbial etiology in a subject that is caused by a fungal infection.
23 cl, 8 tbl, 5 ex
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Authors
Dates
2018-07-24—Published
2017-04-20—Filed