Source:http://linkedlifedata.com/resource/pubmed/id/20346654
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2010-4-5
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pubmed:abstractText |
Non-steroidal compounds that inhibit 17beta-hydroxysteroid dehydrogenase isoform 3 (17beta-HSD3), an enzyme catalyzing the final step in testosterone biosynthesis in Leydig cells, are under development for male contraceptive or treatment of androgen dependent diseases including prostate cancer. A series of curcumin analogues with more stable chemical structures were compared to curcumin as inhibitors of 17beta-HSD3 in rat intact Leydig cells as well as rat and human testis microsomes.
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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 |
Apr
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pubmed:issn |
1464-3405
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2010 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2549-51
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pubmed:meshHeading |
pubmed-meshheading:20346654-17-Hydroxysteroid Dehydrogenases,
pubmed-meshheading:20346654-Animals,
pubmed-meshheading:20346654-Curcumin,
pubmed-meshheading:20346654-Enzyme Inhibitors,
pubmed-meshheading:20346654-Humans,
pubmed-meshheading:20346654-Male,
pubmed-meshheading:20346654-Rats,
pubmed-meshheading:20346654-Testis
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pubmed:year |
2010
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pubmed:articleTitle |
Curcumin derivatives inhibit testicular 17beta-hydroxysteroid dehydrogenase 3.
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pubmed:affiliation |
School of Pharmacy, Wenzhou Medical College, Wenzhou 325000, PR China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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