Authors
Mildred Balbin-Oliveros, Ru Angelie Edrada, Peter Proksch, Victor Wray, Ludger Witte, Rob WM Van Soest
Publication date
1998/7/24
Journal
Journal of natural products
Volume
61
Issue
7
Pages
948-952
Publisher
American Chemical Society
Description
An undescribed Philippine marine sponge of the genus Strongylophora yielded a new meroditerpenoid−strongylophorine dimer (1) and the known meroditerpenoids, strongylophorine-2 (2), strongylophorine-3 (3), and strongylophorine-4 (4). The structures of the compounds were established on the basis of NMR spectroscopic and mass spectrometric data. The position of the inter-unit linkage in the new compound was elucidated after methylation and 1D 1H NOE difference experiments. This is the first report wherein theH and 13C NMR data of the strongylophorine congeners are fully and unambiguously assigned on the basis of 2D NMR spectroscopy. Compounds 2 and 3 exhibited slight activity against Micrococcus luteus and Salmonella typhii, respectively. Compound 3 was active against the phytopathogenic fungus Cladosporium cucumerinum and also against the neonate larvae of the polyphagous pest …
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