Journal
JOURNAL OF NATURAL PRODUCTS
Volume 86, Issue 10, Pages 2407-2413Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.3c00562
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Ibrexafungerp is a new class of antifungal drugs and the first one to be approved in the past 20 years. It is a semi-synthetic derivative of engulfungin, a natural triterpene glycoside that inhibits fungal biosynthesis. The study on Hormonema carpetanum led to the discovery of two new analogues of engulfungin, engulfungins B and C, which may have implications for the biosynthesis of engulfungin. The antifungal activity of engulfungins B and C is lower than that of engulfungin.
Ibrexafungerp, an inhibitor of fungal beta-(1,3)-d-glucan synthase, represents the first new class of antifungals to be approved in the last 20 years. Ibrexafungerp is a semisynthetic derivative of the naturally occurring triterpene glycoside enfumafungin. In order to search for new analogues of enfumafungin and to probe its biosynthesis, we undertook a reinvestigation of Hormonema carpetanum, which led to the isolation of two new analogues, enfumafungins B and C, together with enfumafungin. Due to the presence of a hemiacetal moiety in the structure, the enfumafungins appear as a mixture of two interconverting epimers during both the purification process and NMR data acquisition. The structure elucidation, including the differentiation of 25S* and 25R* epimers, was completed by combined analyses of NMR and MS spectroscopic data. The discovery of enfumafungins B and C may have implications for enfumafungin biosynthesis. The antifungal activity of enfumafungins B and C was significantly lower than that of enfumafungin, suggesting that the C-2 substituents and the C-19 carboxy acid are important for activity. Molecular docking simulations revealed significant hydrogen bond interactions between enfumafungins and beta-(1,3)-d-glucan synthase, which may be useful for developing new antifungal agents.
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