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dc.contributor.authorSingh, K.S.
dc.contributor.authorKaminsky, W.
dc.date.accessioned2011-09-19T10:22:50Z
dc.date.available2011-09-19T10:22:50Z
dc.date.issued2011
dc.identifier.citationNatural Product Communications, vol.6(9); 2011; 1237-1238
dc.identifier.urihttp://drs.nio.org/drs/handle/2264/3910
dc.description.abstractEthyl acetate extract of the sponge Ircinia sp., collected by SCUBA divers off the coast of southern India, contained a cholest-based sterol of insignificant antimicrobial activity, with one carboxylic acid side chain (3 Alpha, 7 Beta-dihydroxy-5 Beta-cholan-24-oic acid, DCA). The structure of the compound was determined by spectroscopic data and single crystal X-ray diffraction studies. DCA crystallizes in the tetragonal space group P4 sub(1) 2 sub(1) 2, chirality documented by solution optical rotation [Alpha] sub(D) =+67.4 degrees (c 0.16, CHCl sub(3)).
dc.language.isoen
dc.publisherNatural Product Communications Inc.
dc.rightsThis is a preprint of an article published in [Natural Product Communications, vol.6(9); 2011; 1237-1238]”. Copyright © 2011 Natural Product Communications.
dc.subjectorganic compounds
dc.subjectchemical extraction
dc.subjectx-ray diffraction analysis
dc.subjectesters
dc.titleIsolation and x-ray structure of deoxycholic acid from the sponge Ircinia sp.
dc.typeJournal Article


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