Source:http://linkedlifedata.com/resource/pubmed/id/12662098
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2003-3-28
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pubmed:abstractText |
The incubation of the diterpene 18-dihydroxy-9,13-epi-ent-pimara-7,15-diene (3) with the fungus Gibberella fujikuroi gave 14 metabolites, 4 and 6-18. The carbons functionalized were the C-20 methyl and all the secondaries, except C-12. The main reaction observed was the epoxidation of the 7,8-double bond, which rearranged to form 7-keto derivatives, such as 10-17, or the allylic alcohol 18. Compound 9 was the only one obtained in which the 7,8-double bond of the substrate remained unaltered. This work confirms that, in the feeding of this type of diterpene with this fungus, the oxidation at C-19, typical of the biosynthesis of gibberellins from ent-kaur-16-ene, is inhibited.
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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 |
Mar
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pubmed:issn |
0163-3864
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
66
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
392-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12662098-Biotransformation,
pubmed-meshheading:12662098-Diterpenes,
pubmed-meshheading:12662098-Gibberella,
pubmed-meshheading:12662098-Gibberellins,
pubmed-meshheading:12662098-Molecular Structure,
pubmed-meshheading:12662098-Nuclear Magnetic Resonance, Biomolecular,
pubmed-meshheading:12662098-Oxidation-Reduction,
pubmed-meshheading:12662098-Stereoisomerism
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pubmed:year |
2003
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pubmed:articleTitle |
Microbial transformation of 18-hydroxy-9,13-epi-ent-pimara-7,15-diene by Gibberella fujikuroi.
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pubmed:affiliation |
Instituto de Productos Naturales y Agrobiología, CSIC, P.O. Box 195, 38206-La Laguna, Tenerife, Canary Islands, Spain. bmfraga@ipna.csic.es
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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