Abstract
Three novel fungal metabolites 1~3 isolated from cultures of a Phoma sp. C2932, are potent and selective inhibitors of squalene synthase. Their structures have been determined by a combination of spectroscopic, X-ray crystallographic and chemical methods; these natural products incorporate the highly functionalised bicyclic core, [lS-(lα,3α,4β,5α,6α,7β)]-4,6,7-trihydroxy-2,8-dioxabicyclo-[3.2. l]octane-3,4,5-tricarboxylic acid. © 1992, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
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CITATION STYLE
Sidebottom, P. J., Highcock, R. M., Lane, S. J., Procopiou, P. A., & Watson, N. S. (1992). The squalestatins, novel inhibitors of squalene synthase produced by a species of phoma: II. structure elucidation. The Journal of Antibiotics, 45(5), 648–658. https://doi.org/10.7164/antibiotics.45.648
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