Salicylanilide acetates: synthesis and antibacterial evaluation
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
PubMed
17693949
PubMed Central
PMC6149344
DOI
10.3390/12010001
PII: 12010001
Knihovny.cz E-zdroje
- MeSH
- antibakteriální látky chemická syntéza chemie farmakologie MeSH
- antifungální látky chemická syntéza chemie farmakologie MeSH
- buněčné linie MeSH
- Candida albicans účinky léků MeSH
- flukonazol farmakologie MeSH
- lidé MeSH
- mikrobiální testy citlivosti MeSH
- mikrobiální viabilita účinky léků MeSH
- molekulární struktura MeSH
- Mycobacterium účinky léků MeSH
- salicylanilidy chemická syntéza chemie farmakologie MeSH
- viabilita buněk účinky léků MeSH
- vztahy mezi strukturou a aktivitou MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antibakteriální látky MeSH
- antifungální látky MeSH
- flukonazol MeSH
- salicylanilide MeSH Prohlížeč
- salicylanilidy 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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