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Arch Pharm (Weinheim) ; 341(10): 655-60, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18720338

ABSTRACT

The N-alkylated derivatives from nitrofurazone were synthesised and evaluated in vitro for their efficacy as antimicrobial agents against representative strains, including methicillin-resistant Staphylococcus aureus (MRSA). The derivative 2a demonstrated greater activity than the prototype and was comparable to currently used antimicrobial drugs.


Subject(s)
Anti-Bacterial Agents , Antifungal Agents , Drug Design , Nitrofurazone , Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Antifungal Agents/chemical synthesis , Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Microbial Sensitivity Tests , Molecular Structure , Nitrofurazone/chemical synthesis , Nitrofurazone/chemistry , Nitrofurazone/pharmacology , Structure-Activity Relationship
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