FIELD: medicine.
SUBSTANCE: invention relates to compounds of general formula (I) or a pharmaceutically acceptable salt thereof, where Z is independently selected and represents a fragment whose structural formula is given below, wherein the asterisk indicates an attachment point; X is independently selected and represents O or S; R1 is independently selected and represents a benzylidene moiety optionally containing 1–3 substituents R', which is independently selected and represent -C1-7-alkyl, -OC1-7-alkyl, halogen, -OH, -C5-7-cycloalkyl, -piperazinyl, optionally containing a substitute selected from -C1-7-alkyl; wherein the asterisk indicates the substitution attachment point; R2 is independently selected and represents H, -C1-7-alkyl, phenyl; said phenyl in fragment R2 is optionally substituted with at least two substitutes, which are halogen; R3 is independently selected and represents halogen; R4 is independently selected and represents halogen; n take values from 0 to 3.
Z: , , , , , ;
R1: .
EFFECT: disclosed compounds are intended for treating and/or preventing an infectious disease of microbial aetiology in a subject caused by a fungal infection, wherein the disease of the microbial aetiology is caused by fungi of the genus Candida speciales, Aspergillus speciales, Microsporum speciales, Trichophyton speciales and/or Epidermophyton speciales.
13 cl, 5 tbl, 56 ex
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Authors
Dates
2019-10-23—Published
2018-12-13—Filed