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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1977-10-28
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pubmed:abstractText |
Microbial transformation experiments have been conducted with the antitumor alkaloid, d-tetrandrine. The alkaloid is selectively demethylated at the N-(2)-position by Cunninghamella blakesleeana ATCC 8688a. The biotransformation reaction is highly selective and uncomplicated by side-product formation. N-demethylation of the alkaloid using methylchloroformate is not regio-specific. Procedures used in screening microorganisms for their abilities to yield metabolites of d-tetrandrine are evaluated.
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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:issn |
0024-5461
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
40
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
239-46
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:895382-Alkaloids,
pubmed-meshheading:895382-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:895382-Fungi,
pubmed-meshheading:895382-Isoquinolines,
pubmed-meshheading:895382-Magnetic Resonance Spectroscopy,
pubmed-meshheading:895382-Molecular Conformation,
pubmed-meshheading:895382-Mucorales,
pubmed-meshheading:895382-Species Specificity,
pubmed-meshheading:895382-Structure-Activity Relationship
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pubmed:articleTitle |
Microbial transformations of natural antitumor agents. IV. Formation of N-(2)-nor-d-tetrandrine by Cunninghamella blakesleeana (ATCC 8688a).
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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