Source:http://linkedlifedata.com/resource/pubmed/id/16300942
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2006-1-9
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pubmed:abstractText |
The monobactam sodium 3-benzylcarbamoyl-2-oxo-1-azetidinesulfonate, bearing a retro (vs classical beta-lactam)-amide side chain, has been synthesized and the kinetics of its reaction with typical beta-lactamases studied. The new compound is generally a poorer substrate than the analogous compound with a normal side chain but its formation of a transiently stable complex with a class C beta-lactamase sustains the retro-amide side-chain concept.
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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 |
Feb
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
869-71
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16300942-Amides,
pubmed-meshheading:16300942-Catalysis,
pubmed-meshheading:16300942-Enterobacter cloacae,
pubmed-meshheading:16300942-Hydrolysis,
pubmed-meshheading:16300942-Kinetics,
pubmed-meshheading:16300942-Molecular Conformation,
pubmed-meshheading:16300942-Monobactams,
pubmed-meshheading:16300942-Stereoisomerism,
pubmed-meshheading:16300942-Structure-Activity Relationship,
pubmed-meshheading:16300942-beta-Lactamases
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pubmed:year |
2006
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pubmed:articleTitle |
Synthesis and reactivity with beta-lactamases of a monobactam bearing a retro-amide side chain.
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pubmed:affiliation |
Department of Chemistry, Wesleyan University, Middletown, CT 06459, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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