Source:http://linkedlifedata.com/resource/pubmed/id/16170778
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2005-10-3
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pubmed:abstractText |
Two new dammarane triterpenoids, 20R,21-epoxydammar-24-ene-3,23-dione and 20R,21-epoxy-3beta-hydroxydammar-24-ene-23-one have been isolated from the aerial parts of Kageneckia angustifolia D. Don, Rosaceae, along with the previously reported triterpenoids oleanolic acid and 3beta-(beta-D-glucosyloxy)-16alpha,23alpha-epoxycucurbita-5,24-dien-11-one and the phenolic prunasin. The structures of these compounds were established by MS, 1D- and 2D-NMR experiments, and the structure of the new compounds were confirmed by X-ray diffraction analysis.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0749-1581
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pubmed:author | |
pubmed:copyrightInfo |
Copyright (c) 2005 John Wiley & Sons, Ltd.
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pubmed:issnType |
Print
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
943-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16170778-Carbon Isotopes,
pubmed-meshheading:16170778-Crystallography, X-Ray,
pubmed-meshheading:16170778-Magnetic Resonance Spectroscopy,
pubmed-meshheading:16170778-Models, Molecular,
pubmed-meshheading:16170778-Molecular Conformation,
pubmed-meshheading:16170778-Protons,
pubmed-meshheading:16170778-Reference Standards,
pubmed-meshheading:16170778-Rosaceae,
pubmed-meshheading:16170778-Stereoisomerism,
pubmed-meshheading:16170778-Triterpenes
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pubmed:year |
2005
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pubmed:articleTitle |
Two new dammarane triterpenoids from Kageneckia angustifolia D. Don.
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pubmed:affiliation |
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Salamanca, E-37007 Salamanca, Spain. lopez@usal.es
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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