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Hymenopsins A and B and a macrophorin analogue from a fungicolous Hymenopsis sp
Journal article   Peer reviewed

Hymenopsins A and B and a macrophorin analogue from a fungicolous Hymenopsis sp

Lori E Schmidt, Stephen T Deyrup, Jonas Baltrusaitis, Dale C Swenson, Donald T Wicklow and James B Gloer
Journal of natural products (Washington, D.C.), Vol.73(3), pp.404-408
03/26/2010
DOI: 10.1021/np900613d
PMCID: PMC2846221
PMID: 19928955
url
https://www.ncbi.nlm.nih.gov/pmc/articles/2846221View
Open Access

Abstract

Hymenopsin A (1), hymenopsin B (2), and a new macrophorin analogue, 2',3'-epoxy-13-hydroxy-4'-oxomacrophorin A (3), have been isolated from a fungicolous isolate of Hymenopsis sp. (MYC-1703; NRRL 37638). The structures and relative configurations of these compounds were assigned on the basis of 2D NMR and MS data, and the identity of 1 was confirmed by X-ray crystallographic analysis. The absolute configuration of 2 was proposed on the basis of CD analysis using both empirical and computational methods. Compounds 2 and 3 showed antibacterial activity against Staphylococcus aureus and Bacillus subtilis. Compound 3 was also active against Aspergillus flavus and Fusarium verticillioides.
Sesquiterpenes - isolation & purification Sesquiterpenes - chemistry Molecular Conformation Hawaii Crystallography, X-Ray Structure-Activity Relationship Fungi - chemistry Microbial Sensitivity Tests Nuclear Magnetic Resonance, Biomolecular Molecular Structure Sesquiterpenes - pharmacology Staphylococcus aureus - drug effects Bacillus subtilis - drug effects

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