Abstract
Micafungin is the second approved antifungal agent in the echinocandin series and is now used worldwide in chemotherapy for life-threatening fungal infections. It is water-soluble and is semi-synthesized from the acylated cyclic hexapeptide FR901379, a natural product from the fungus Coleophoma empetri F-11899, through enzymatic deacylation of FR901379, followed by chemical reacylation with the optimized N-acyl side chain. The water solubility of micafungin is ascribed to a sulfate moiety in the molecule. This feature differentiates micafungin from other echinocandin members. Micafungin is a potent inhibitor of 1,3-β-glucan synthase, an enzyme necessary for cell-wall synthesis of several fungal pathogens. © 2009 Japan Antibiotics Research Association All rights reserved.
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CITATION STYLE
Hashimoto, S. (2009, January). Micafungin: A sulfated echinocandin. Journal of Antibiotics. https://doi.org/10.1038/ja.2008.3
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