| Literature DB >> 12608864 |
Peter Schupp1, Timo Poehner, RuAngelie Edrada, Rainer Ebel, Albrecht Berg, Victor Wray, Peter Proksch.
Abstract
Chemical investigation of the Micronesian ascidian Eudistoma sp. afforded two new eudistomin congeners, which were designated eudistomins W (1) and X (2). The structures of the new compounds were unambiguously established on the basis of NMR spectroscopic ((1)H, (13)C, COSY, (1)H detected direct, and long-range (13)C-(1)H correlations) and mass spectrometric (EI and ESIMS) data. Compound 2 exhibited antibiotic activity toward Bacillus subtilis, Staphyloccocus aureus, and Escherichia coli and was also found to be fungicidal against Candida albicans in an agar diffusion assay. Compound 1 was selectively active against C. albicans but showed no antibacterial activity.Entities:
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Year: 2003 PMID: 12608864 DOI: 10.1021/np020315n
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050