Source:http://linkedlifedata.com/resource/pubmed/id/16246555
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2005-12-26
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pubmed:abstractText |
The synthesis of a series of maslinic acid derivatives is described and their effect on rabbit muscle glycogen phosphorylase a evaluated. Within this series of compounds, 15 (IC(50)=7 microM) is the most potent GPa inhibitor. SAR of the maslinic acid derivatives are discussed.
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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 |
Feb
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
722-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16246555-Animals,
pubmed-meshheading:16246555-Enzyme Inhibitors,
pubmed-meshheading:16246555-Glycogen Phosphorylase, Muscle Form,
pubmed-meshheading:16246555-Muscles,
pubmed-meshheading:16246555-Rabbits,
pubmed-meshheading:16246555-Structure-Activity Relationship,
pubmed-meshheading:16246555-Triterpenes
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pubmed:year |
2006
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pubmed:articleTitle |
Pentacyclic triterpenes. Part 2: Synthesis and biological evaluation of maslinic acid derivatives as glycogen phosphorylase inhibitors.
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pubmed:affiliation |
Department of Medicinal Chemistry, College of Pharmacy, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Evaluation Studies
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