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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
1990-10-4
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pubmed:abstractText |
Several 3'-substituted cephalosporin sulfones were synthesized from 3-(hydroxymethyl)cephalosporin, which was prepared by Ti(OiPr)4 hydrolysis of the corresponding acetate. A method was also developed to prepare a 3-vinylcephalosporin. Some of these compound were found to be potent time-dependent inhibitors of human leukocyte elastase (HLE). The HLE inhibitory activity was correlated with sigma 1 and it was concluded that the potency was determined by the electron-withdrawing ability as well as the size of the substituent. A mechanism for inhibition of HLE by cephalosporin sulfones 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 |
Sep
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pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2529-35
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:2391693-Cephalosporins,
pubmed-meshheading:2391693-Chemical Phenomena,
pubmed-meshheading:2391693-Chemistry,
pubmed-meshheading:2391693-Humans,
pubmed-meshheading:2391693-Leukocyte Elastase,
pubmed-meshheading:2391693-Pancreatic Elastase,
pubmed-meshheading:2391693-Structure-Activity Relationship,
pubmed-meshheading:2391693-Sulfones
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pubmed:year |
1990
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pubmed:articleTitle |
Inhibition of human leukocyte elastase. 3. Synthesis and activity of 3'-substituted cephalosporins.
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pubmed:affiliation |
Department of Medicinal Chemical Research, Merck Sharp and Dohme Research Laboratories, Rahway, New Jersey 07065.
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pubmed:publicationType |
Journal Article
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