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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
1987-12-9
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pubmed:abstractText |
The enantiomers of beta,gamma-dimethyl- and beta-methyl-alpha-methylene-gamma-butyrolactones have been synthesized stereospecifically from glutamic acid and beta-hydroxy isobutyric acid, respectively. Guinea pigs have been sensitized (Freund complete adjuvant technique) and tested to them. Both enantiomers of beta-methyl lactone as well as (+)-beta,gamma-dimethyl lactone induced enantiospecific allergic contact dermatitis (ACD); in turn, (-)-beta,gamma-dimethyl lactone showed no specificity. An interpretation is proposed.
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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 |
Nov
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pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
30
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1948-51
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:3669003-4-Butyrolactone,
pubmed-meshheading:3669003-Allergens,
pubmed-meshheading:3669003-Animals,
pubmed-meshheading:3669003-Dermatitis, Contact,
pubmed-meshheading:3669003-Female,
pubmed-meshheading:3669003-Furans,
pubmed-meshheading:3669003-Guinea Pigs,
pubmed-meshheading:3669003-Skin Tests,
pubmed-meshheading:3669003-Stereoisomerism,
pubmed-meshheading:3669003-Structure-Activity Relationship
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pubmed:year |
1987
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pubmed:articleTitle |
Stereospecificity in allergic contact dermatitis to simple substituted methylene lactone derivatives.
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pubmed:affiliation |
Laboratoire de Dermato-Chimie, Université Louis Pasteur, CHU, Strasbourg, France.
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pubmed:publicationType |
Journal Article
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