Source:http://linkedlifedata.com/resource/pubmed/id/17067176
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2006-10-27
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pubmed:abstractText |
Four new oxindole alkaloids, paratunamides A-D (1-4), containing a secologanin unit, were isolated from the bark of Cinnamodendron axillare, and their structures and relative configurations were elucidated by spectroscopic data. The absolute configuration at C-7 in 1-4 was assigned as S, S, R, and S, respectively, on the basis of the CD spectra.
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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 |
Oct
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pubmed:issn |
0163-3864
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1517-21
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pubmed:meshHeading |
pubmed-meshheading:17067176-Brazil,
pubmed-meshheading:17067176-Indole Alkaloids,
pubmed-meshheading:17067176-Magnoliaceae,
pubmed-meshheading:17067176-Molecular Structure,
pubmed-meshheading:17067176-Nuclear Magnetic Resonance, Biomolecular,
pubmed-meshheading:17067176-Plant Bark,
pubmed-meshheading:17067176-Plants, Medicinal
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pubmed:year |
2006
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pubmed:articleTitle |
Paratunamides A-D, oxindole alkaloids from Cinnamodendron axillare.
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pubmed:affiliation |
Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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