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Chem Pharm Bull (Tokyo) ; 55(2): 236-40, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17268095

ABSTRACT

Urea and thiourea derivatives of oxazolidinones were synthesized and their inhibitory activity (MIC) was determined on the bacterial strains which includes clinical isolates and quality control organisms. The structure activity relationships were studied and a 3D-QSAR model was built using Genetic Function Approximation. Interestingly found that electron withdrawing groups at the ortho position of the phenyl ring enhances the activity.


Subject(s)
Anti-Bacterial Agents/pharmacology , Enterococcus faecalis/drug effects , Oxazolidinones/pharmacology , Staphylococcus/drug effects , Thiourea/chemistry , Urea/chemistry , Anti-Bacterial Agents/chemical synthesis , Drug Resistance, Microbial , Microbial Sensitivity Tests , Oxazolidinones/chemical synthesis , Quantitative Structure-Activity Relationship
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