期刊
ARCHIV DER PHARMAZIE
卷 344, 期 12, 页码 794-801出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ardp.201000224
关键词
Anti-Candida; Grignard reaction; Imidazoles; Mannich reaction
The synthesis and anti-Candida activity of 1-[(3-aroyloxy-3-phenyl)propyl]-1H-imidazoles 5af and 1-[(3-alkyl/aralkyl/phenyl-3-phenyl)propan-3-ol]-1H-imidazoles 5gj are reported. The influence of the ester formation and different substitutions on the anti-Candida activity of the alcohol 4 was investigated. Among the newly developed bioactive chemical entities, compounds 5b and 5c displayed minimum inhibitory concentrations (MICs) against Candida albicans and Candida pseudotropicales comparable to that of tioconazole and more potent than miconazole.
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