Si-Lu Hua , Ping Liu , Xing-Chen Zhang , Li Miao , Xiao-Jian Zhou , Dongdong Wang , Wei Jiang
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引用次数: 0
Abstract
Three new furanone derivatives, named paraconfuranones N–P (1–3) were obtained from an EtOAc extract of a marine-derived fungus Paraconiothyrium sporulosum DL-16. Their structures, including absolute configurations, were elucidated by extensive NMR spectroscopic and MS spectrometric analyses, modified Mosher's method, and ECD computational studies. Compounds 1–3 showed significant inhibitory activities against four strains of Gram-positive bacteria Staphylococcus aureus, and one strain of Gram-negative bacterium Vibrio parahaemolyticus, with MIC values ranging from 3.125 to 6.25 μg/mL, comparable to the positive controls, but none of them showed activity on the strains of Enterococcus faecalis, E. faecium, and Escherichia coli.
期刊介绍:
Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry.
Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters.
Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.