| Literature DB >> 21958335 |
Susanna T S Chan1, A Norrie Pearce, Ana H Januario, Michael J Page, Marcel Kaiser, Rene J McLaughlin, Jacquie L Harper, Victoria L Webb, David Barker, Brent R Copp.
Abstract
Bioassay-directed fractionation of an extract of the New Zealand ascidian Aplidium scabellum has afforded the anti-inflammatory secondary metabolite 2-geranyl-6-methoxy-1,4-hydroquinone-4-sulfate (1) and a family of pseudodimeric meroterpenoids scabellones A (2)-D (5). The benzo[c]chromene-7,10-dione scaffold contained within scabellones A-D is particularly rare among natural products. The structures were elucidated by interpretation of NMR data. Scabellone B was also identified as a moderately potent, nontoxic inhibitor of Plasmodium falciparum.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21958335 DOI: 10.1021/jo201654h
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354