Cladosporin, a new antifungal metabolite from cladosporium cladosporioides

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Abstract

Cladosporin is a new fungal metabolite produced in good yield in the mycelium of Cladosporium cladosporioid s (Fres.) de Vries. Its structure was established as 3,4-dihydro-6,8-dihydroxy-3-(tetrahydro-6-methyl-2H-pyra-2-yl)methylisocoumarin on the basis of spectroscopic studies of the parent compound, mono- and di-methyl derivatives, and a monoacetate. Both cladosporin and monoacetyl cladosporin completely inhibited growth of severa dermatophytes on agar medium at a concentration of 75 μg/ml. The germination of spores from several Fenicillium and Aspergillus spp. was inhibited by these compounds at concentrations of 40 μg/ml or less in liquid medium. © 1971, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.

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Scott, P. M., Van Walbeek, W., & MacLean, W. M. (1971). Cladosporin, a new antifungal metabolite from cladosporium cladosporioides. The Journal of Antibiotics, 24(11), 747–755. https://doi.org/10.7164/antibiotics.24.747

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