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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 no: | Antimicrob Agents Chemother |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Microbiology (ASM)
1980
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| Assuntos: | |
| Acesso em linha: | 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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