Source:http://linkedlifedata.com/resource/pubmed/id/21751846
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
8
|
| pubmed:dateCreated |
2011-7-14
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| pubmed:abstractText |
The chemical study of endophytic fungus of Cochliobolus led to the isolation of 10 terpenes (1-10), including one new compound named isocochlioquinone B (1). Their structures were elucidated on the basis of spectroscopic methods, including 2D NMR techniques. Compounds 5-7 showed significant neuraminidase inhibitory activity with IC(50) values of 0.79-1.75 ?M.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
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| pubmed:month |
Aug
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| pubmed:issn |
1477-2213
|
| pubmed:author | |
| pubmed:issnType |
Electronic
|
| pubmed:volume |
13
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
761-4
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| pubmed:meshHeading |
pubmed-meshheading:21751846-Ascomycota,
pubmed-meshheading:21751846-Benzoquinones,
pubmed-meshheading:21751846-Inhibitory Concentration 50,
pubmed-meshheading:21751846-Molecular Structure,
pubmed-meshheading:21751846-Neuraminidase,
pubmed-meshheading:21751846-Nuclear Magnetic Resonance, Biomolecular,
pubmed-meshheading:21751846-Oseltamivir,
pubmed-meshheading:21751846-Terpenes
|
| pubmed:year |
2011
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| pubmed:articleTitle |
Neuraminidase inhibitory terpenes from endophytic Cochliobolus sp.
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| pubmed:affiliation |
State Key Laboratory of Pharmaceutical Biotechnology, Institute of Functional Biomolecules, Nanjing University, Nanjing, China.
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| pubmed:publicationType |
Journal Article
|