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J Enzyme Inhib Med Chem ; 27(6): 849-53, 2012 Dec.
Article in English | MEDLINE | ID: mdl-21988189

ABSTRACT

A series of 3-[3-(substituted phenyl)-1-phenyl-1H-pyrazol-5-yl]-2H-chromen-2-one (4a-k) were synthesized by reaction of 3-[2,3-dibromo-3-(substituted phenyl)propanoyl]-2H-chromen-2-one (3 a-k) with phenyl hydrazine in presence of triethylamine in absolute ethanol, characterized by spectral data and screened for their in vitro antibacterial activity against gram-positive and gram-negative bacteria. Among the series, compounds 4d, 4h and 4i displayed an encouraging antibacterial activity profile as compared to reference standard drug ciprofloxacin against tested bacterial strains.


Subject(s)
Anti-Bacterial Agents/chemical synthesis , Bacillus subtilis/drug effects , Benzopyrans/chemical synthesis , Escherichia coli/drug effects , Pseudomonas aeruginosa/drug effects , Pyrazoles/chemical synthesis , Staphylococcus aureus/drug effects , Anti-Bacterial Agents/pharmacology , Bacillus subtilis/growth & development , Benzopyrans/pharmacology , Ciprofloxacin/pharmacology , Escherichia coli/growth & development , Ethanol/chemistry , Ethylamines/chemistry , Microbial Sensitivity Tests , Microbial Viability/drug effects , Phenylhydrazines/chemistry , Pseudomonas aeruginosa/growth & development , Pyrazoles/pharmacology , Staphylococcus aureus/growth & development , Structure-Activity Relationship
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