
doi: 10.1021/np050074u
pmid: 16124777
A series of 29 artemisinin derivatives (2-30), including four new compounds (16-18, 20), together with artemisinin (1), artemisinic acid (31), and arteannuin B (32), were tested for antifungal activity against two opportunistic pathogens, Candida albicans and Cryptoccocus neoformans. Of all the compounds tested, anhydrodihydro-artemisinin (3) demonstrated more potent antifungal activity against C. neoformans than amphotericin B. Also, beta-arteether (7) and alpha-arteether (8) showed marked activity against C. neoformans. Against C. albicans, the overall antifungal effect of these compounds was weak or negligible. Derivatives 2-30 were prepared according to literature procedures.
Antifungal Agents, Molecular Structure, Candida albicans, Cryptococcus neoformans, Combinatorial Chemistry Techniques, Microbial Sensitivity Tests, Artemisinins
Antifungal Agents, Molecular Structure, Candida albicans, Cryptococcus neoformans, Combinatorial Chemistry Techniques, Microbial Sensitivity Tests, Artemisinins
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