O-aryloxycarbonyl hydroxamates: new beta-lactamase inhibitors that cross-link the active site. Research Abstract Details
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Pauline N Wyrembak,Kerim Babaoglu,Ryan B Pelto,Brian K Shoichet,R F Pratt,
PN Wyrembak,K Babaoglu,RB Pelto,BK Shoichet,RF Pratt,
For similar enzymes and coenzymes: enzymes: hydrolases: amidohydrolases: beta-lactamases research abstracts see: enzymes and coenzymes: enzymes: hydrolases: amidohydrolases: beta-lactamases research
PUBMED ID PMID:
MEDLINE DATE:
PUBLICATION TYPE: Research Support, N.I.H., Extr
Journal: Journal of the American Chemical Society
VOLUME: 129
Page Numbers: 9548-9
Journal Abbreviation: J. Am. Chem. Soc.
ISSN: 0002-7863
DAY: 12
MONTH: 07
YEAR: 2007
Number of References:
LANGUAGE: eng
NlmUniqueID: 7503056
KEYWORDS: beta-Lactamases
MESH TERMS: metabolism
Substance Name: beta-Lactamases
Registry Number: EC 3.5.2.6
AFFILIATION: Department of Chemistry, Wesleyan University, Middletown, Connecticut 06459, USA.
Country: United States
AGENCY: United States NIGMS
GRANT: GM 63815
ACRONYM: GM
MEDLINETA: J Am Chem Soc
REFSOURCE:
DATABASENAME:
ACCESSION NUMBER:
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