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Effect of 7 alpha substitution of cephems on their beta-lactamase stability and affinity for penicillin-binding proteins in Morganella morganii.

Cephamycins, which have a methoxy group at the 7 alpha position of their cephalosporin nuclei, were highly stable against hydrolysis by a beta-lactamase purified from a clinical isolate of Morganella morganii, whereas their 7 alpha-H analogs were rapidly hydrolyzed by the enzyme. The high stability...

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Bibliografiske detaljer
Udgivet i:Antimicrob Agents Chemother
Principais autores: Ohya, S, Yamazaki, M, Sugawara, S
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Microbiology (ASM) 1983
Fag:
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC184692/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6602587/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/aac.23.4.522
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