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Inhibitors of biosynthesis of cholesterol and ergosterol, method of preparation and use thereof

机译:胆固醇和麦角固醇的生物合成抑制剂,其制备方法和用途

摘要

Described are N-alkyl substituted pyrrolidin- benzoheterocyclic compounds of the general formula (I), wherein R1 is hydrogen, methyl, ethyl, propyl and allyl, R2 is halogen atom (F, Cl, Br, I), methoxy, nitro, cyano, amino and trifluoromethyl, Y is N or CH and Z is CH2, CH2CH2, CH=CH, O, S, SO, SO2 and NCH3 and their pharmaceutically acceptable salts; a method of preparation thereof and their use as inhibitors of biosynthesis of cholesterol and ergosterol.
机译:描述了通式(I)的N-烷基取代的吡咯烷基-苯并杂环化合物,其中R 1是氢,甲基,乙基,丙基和烯丙基,R 2是卤素原子(F,Cl,Br,I),甲氧基,硝基,氰基,氨基和三氟甲基,Y为N或CH,Z为CH 2,CH 2 CH 2,CH = CH,O,S,SO,SO 2和NCH 3及其药学上可接受的盐;制备方法及其作为胆固醇和麦角固醇的生物合成抑制剂的用途。

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