| Literature DB >> 15610892 |
Guoqiang Li1, Zhiwei Deng, Huashi Guan, Leen van Ofwegen, Peter Proksch, Wenhan Lin.
Abstract
Fifteen steroids were isolated from the soft coral Dendronephthya sp., of which five are determined as new compounds, namely (22E)-3-O-beta-formylcholest-5,22-diene (1), (22E)-3-O-beta-formyl-24-methyl-cholest-5,22-diene (2), 2-ethoxycarbonyl-2-beta-hydroxy-A-nor-cholest-5-ene-4-one (3), (22E)-2-ethoxycarbonyl-2-beta-hydroxy-A-nor-cholest-5,22-diene-4-one (4), and (22E)-2-ethoxycarbonyl-2-beta-hydroxy-24-mthyl-A-nor-cholest-5,22-diene-4- one (5). 1 and 2 belonged to 3-O-formylated cholesterol analogues, and 3 to 5 are unique ring A-contracted steroids. Their structures were elucidated by extensive 2D NMR in association with IR, MS analysis.Entities:
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Year: 2004 PMID: 15610892 DOI: 10.1016/j.steroids.2004.09.003
Source DB: PubMed Journal: Steroids ISSN: 0039-128X Impact factor: 2.668