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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
10
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pubmed:dateCreated |
1995-1-25
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pubmed:abstractText |
The conjugation products of E-destruxin (cyclodepsipeptide) with glutathione have been identified by fast-atom bombardment mass spectrometry. Appropriate conditions were developed for cyclodepsipeptide substrate, which enabled the direct, dynamic mass spectra analysis of spontaneous as well as glutathione-s-transferase catalyzed conjugation reactions. Application to the most active cyclopeptide in the series of destruxins yielded glutathionyl adduct.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0951-4198
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
844-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8000080-Amino Acid Sequence,
pubmed-meshheading:8000080-Depsipeptides,
pubmed-meshheading:8000080-Fungal Proteins,
pubmed-meshheading:8000080-Glutathione,
pubmed-meshheading:8000080-Glutathione Transferase,
pubmed-meshheading:8000080-Mitosporic Fungi,
pubmed-meshheading:8000080-Molecular Sequence Data,
pubmed-meshheading:8000080-Mycotoxins,
pubmed-meshheading:8000080-Peptides, Cyclic,
pubmed-meshheading:8000080-Spectrometry, Mass, Fast Atom Bombardment
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pubmed:year |
1994
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pubmed:articleTitle |
Conjugation reactions of cyclodepsipeptide to glutathionyl adducts by direct 'in-beam' synthesis under negative-ion fast-atom bombardment conditions.
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pubmed:affiliation |
Département de Chimie, Université de Versailles, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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