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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
1998-11-13
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pubmed:abstractText |
The study on structure-activity relationship of saikosaponins and glycyrrhizin derivatives for Na+, K(+)-ATPase inhibiting action has been made in vitro. The results showed that the order of potency of inhibitory effect of saikosaponins on Na+, K(+)-ATPase is as follows: b1 > d > b2 > b4 > a > b3 > e > c. The chemical structure C23-OH, C16-OH and the C11, C13 conjugated double diene of saikosaponins are important for its inhibitory activity. The inhibitory potency of glycyrrhizin (GL), glycyrrhetinic acid (GA) and carbenoxolone (CX) for Na+, K(+)-ATPase activity is as follows: GA > or = CX > GL. In addition, the inhibitory effect of saikosaponin d on Na+, K(+)-ATPase was found to be non-competitive.
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pubmed:language |
chi
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Glycyrrhizic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Oleanolic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Sapogenins,
http://linkedlifedata.com/resource/pubmed/chemical/Saponins,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium-Potassium-Exchanging ATPase,
http://linkedlifedata.com/resource/pubmed/chemical/saikosaponin
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pubmed:status |
MEDLINE
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pubmed:issn |
0513-4870
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
496-501
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9772691-Cell-Free System,
pubmed-meshheading:9772691-Glycyrrhizic Acid,
pubmed-meshheading:9772691-Humans,
pubmed-meshheading:9772691-Oleanolic Acid,
pubmed-meshheading:9772691-Sapogenins,
pubmed-meshheading:9772691-Saponins,
pubmed-meshheading:9772691-Sodium-Potassium-Exchanging ATPase,
pubmed-meshheading:9772691-Structure-Activity Relationship
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pubmed:year |
1996
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pubmed:articleTitle |
[The structure activity relationship of saikosaponins and glycyrrhizin derivatives for Na+, K(+)-ATPase inhibiting action].
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pubmed:affiliation |
Institute of Preclinical Sciences, Norman Bethune University of Medical Sciences, Changchun.
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pubmed:publicationType |
Journal Article,
English Abstract
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