Source:http://linkedlifedata.com/resource/pubmed/id/17904850
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
24
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pubmed:dateCreated |
2007-10-22
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pubmed:abstractText |
Two novel C(27)N(3)-type Lycopodium alkaloids, cryptadines A (1) and B (2) consisting of two octahydroquinoline rings (C(11)N) and a piperidine ring (C(5)N), have been isolated from the club moss Lycopodium cryptomerinum, and their structures and relative stereochemistry were elucidated on the basis of spectroscopic data, chemical transformations, and computational methods. Cryptadines A (1) and B (2) exhibited an inhibitory activity against acetylcholinesterase.
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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 |
Dec
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pubmed:issn |
1464-3391
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7803-8
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pubmed:meshHeading |
pubmed-meshheading:17904850-Alkaloids,
pubmed-meshheading:17904850-Computer Simulation,
pubmed-meshheading:17904850-Cyclization,
pubmed-meshheading:17904850-Lycopodium,
pubmed-meshheading:17904850-Magnetic Resonance Spectroscopy,
pubmed-meshheading:17904850-Molecular Structure,
pubmed-meshheading:17904850-Piperidines,
pubmed-meshheading:17904850-Quinolines
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pubmed:year |
2007
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pubmed:articleTitle |
Cryptadines A and B, novel C27N3-type pentacyclic alkaloids from Lycopodium cryptomerinum.
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pubmed:affiliation |
Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41 Shinagawa, Tokyo 142-8501, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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