Journal of Chemistry · 2012 · 48 citations · 22 references
PharmacyMedicinal ChemistryDrug DiscoveryStructure-activity RelationshipsSynthetic Medicinal ChemistryAntimicrobial Spectrum Of ActivityStructure-activity Relationship AnalysisAntioxidant Activity AssaysAntioxidant Natural ProductsAntioxidant PropertiesAntioxidantsNatural AntioxidantsScavenging
A series of β ‐Isatin aldehyde‐N,N ′ ‐thiocarbohydrazone derivatives were synthesized and assayed for their in vitro antimicrobial and antioxidant activity. The new compounds were characterized based on spectral (FT‐IR, NMR, MS) analyses. All the test compounds possessed a broad spectrum of activity having MIC values rangeing from 12.5 to 400 μ g/ml against the tested microorganisms. Among the compounds 3e , 3j and 3n show highest significant antimicrobial activity. The free radical scavenging effects of the test compounds against stable free radical DPPH ( α , α ‐diphenyl‐ β ‐picryl hydrazyl) and H 2 O 2 were measured spectrophotometrically. Compounds 3j , 3n , 3l , and 3e , respectively, had the most effective antioxidant activity against DPPH and H 2 O 2 scavenging activity.
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Antioxidant Determinations by the Use of a Stable Free Radical
Marsden S. Blois · Nature · 1958 · 12.8K citations
Biological activities of isatin and its derivatives.
Surendra N. Pandeya, Sivakumar Smitha, Mayank Jyoti et al. · PubMed · 2005 · 345 citations · Full text