Abstract
Some benzimidazole derivatives namely 1-[(substituted thiocarbamoylhydrazine carbonyl) methyl]-2-phenyl-1H-benzimidazoles (1a-13a), N-[(2-phenylbenzimidazol-1-yl methyl)-[1,3,4]-thiadiazole-2-yl]-substituted phenyl amines (1b-13b) and 5-(2-phenyl benzimidazol-1-yl-methyl)-4-substituted phenyl-4H-1,2,4-triazole-3-thiones (1c-13c) were synthesized, and their in vitro effects on the rat liver microsomal NADPH-dependent lipid peroxidation (LP) levels were determined. The most active compound 10a caused an 84% inhibition of LP at 10(-3) M, which is better than that of butylated hydroxytoluene (BHT) (65%).
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antioxidants / chemical synthesis*
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Antioxidants / pharmacology*
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Benzimidazoles / chemical synthesis*
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Benzimidazoles / pharmacology*
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Chemical Phenomena
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Chemistry, Physical
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In Vitro Techniques
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Indicators and Reagents
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Lipid Peroxidation / drug effects*
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Liver / drug effects
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Liver / metabolism*
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Magnetic Resonance Spectroscopy
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Male
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Mass Spectrometry
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NADP / metabolism
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Rats
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Semicarbazides / chemical synthesis
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Semicarbazides / pharmacology
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Spectrophotometry, Infrared
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Thiadiazoles / chemical synthesis
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Thiadiazoles / pharmacology
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Triazoles / chemical synthesis
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Triazoles / pharmacology
Substances
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Antioxidants
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Benzimidazoles
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Indicators and Reagents
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Semicarbazides
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Thiadiazoles
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Triazoles
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NADP