Source:http://linkedlifedata.com/resource/pubmed/id/12596876
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2003-2-24
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pubmed:abstractText |
Zearalenones are mycotoxins with estrogenic activity consisting of a resorcinol moiety fused to a 14-membered macrocyclic lactone and are produced by various Fusarium species. We found that Clonostachys rosea IFO 7063 was effectively capable of converting zearalenone (1) to cleavage product (2), 1-(3,5-dihydroxyphenyl)-10'-hydroxy-1'E-undecene-6'-one. Moreover, cleavage product 2 did not show potent estrogenic activity like that of 1 and 17beta-estradiol in the human breast cancer MCF-7 cell proliferation assay.
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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 |
Dec
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pubmed:issn |
0916-8451
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
66
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2723-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12596876-Ascomycota,
pubmed-meshheading:12596876-Biotransformation,
pubmed-meshheading:12596876-Breast Neoplasms,
pubmed-meshheading:12596876-Cell Division,
pubmed-meshheading:12596876-Estrogens,
pubmed-meshheading:12596876-Humans,
pubmed-meshheading:12596876-Ketones,
pubmed-meshheading:12596876-Magnetic Resonance Spectroscopy,
pubmed-meshheading:12596876-Molecular Structure,
pubmed-meshheading:12596876-Resorcinols,
pubmed-meshheading:12596876-Tumor Cells, Cultured,
pubmed-meshheading:12596876-Zearalenone
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pubmed:year |
2002
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pubmed:articleTitle |
Biotransformation of the mycotoxin, zearalenone, to a non-estrogenic compound by a fungal strain of Clonostachys sp.
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pubmed:affiliation |
Antibiotics Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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