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In vitro activity of chloramphenicol and thiamphenicol analogs.

The in vitro activity of three fluorine analogs of chloramphenicol in which the hydroxyl group at position 3 had been replaced with a fluorine was compared with that of chloramphenicol and thiamphenicol. Compound SCH 24893 was the most active agent against staphylococci and Bacteroides strains, and...

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Publicado en:Antimicrob Agents Chemother
Autores principales: Neu, H C, Fu, K P
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society for Microbiology (ASM) 1980
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Acceso en línea:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC283989/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7447408/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/aac.18.2.311
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