Salicylanilide acetates: synthesis and antibacterial evaluation
Language English Country Switzerland Media electronic
Document type Journal Article
PubMed
17693949
PubMed Central
PMC6149344
DOI
10.3390/12010001
PII: 12010001
Knihovny.cz E-resources
- MeSH
- Anti-Bacterial Agents chemical synthesis chemistry pharmacology MeSH
- Antifungal Agents chemical synthesis chemistry pharmacology MeSH
- Cell Line MeSH
- Candida albicans drug effects MeSH
- Fluconazole pharmacology MeSH
- Humans MeSH
- Microbial Sensitivity Tests MeSH
- Microbial Viability drug effects MeSH
- Molecular Structure MeSH
- Mycobacterium drug effects MeSH
- Salicylanilides chemical synthesis chemistry pharmacology MeSH
- Cell Survival drug effects MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Antifungal Agents MeSH
- Fluconazole MeSH
- salicylanilide MeSH Browser
- Salicylanilides MeSH
A new series of salicylanilide acetates was synthesized and evaluated for their in vitro antifungal and antituberculotic activity. Some of the evaluated compounds possessed comparable or better antifungal activity than a fluconazole standard. All these compounds exhibited very good potential and their in vitro activity against drug resistant and sensitive clinical isolates of Mycobacteria were found to be equivalent or better than a standard of isoniazide, a well-known first-line drug for tuberculosis treatment.
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