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Pak J Pharm Sci ; 29(3): 811-7, 2016 May.
Article in English | MEDLINE | ID: mdl-27166526

ABSTRACT

Pyrazine carbohydrazide based hydrazones were synthesized starting from 5-methylpyrazine-2-carboxylic acid. The acid was first converted to its methyl ester, which on further treatment with hydrazine hydrate transformed to carbohydrazide. The carbohydrazide was treated with differently substituted aromatic carbonyl compounds giving hydrazones. Characterization of the synthesized compounds was carried out using modern spectroscopic techniques and unambiguously confirmed through X-ray crystallographic studies of compound 3d. The purity of the compounds was verified using elemental analysis. The target molecules were evaluated for urease inhibition, antioxidant and antimicrobial activity.


Subject(s)
Drug Design , Hydrazines/chemical synthesis , Hydrazines/pharmacology , Hydrazones/chemical synthesis , Hydrazones/pharmacology , Pyrazines/chemical synthesis , Pyrazines/pharmacology , Anti-Infective Agents/chemical synthesis , Anti-Infective Agents/pharmacology , Antioxidants/chemical synthesis , Antioxidants/pharmacology , Carbon-13 Magnetic Resonance Spectroscopy , Crystallography, X-Ray , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/pharmacology , Mass Spectrometry , Models, Molecular , Molecular Structure , Proton Magnetic Resonance Spectroscopy , Spectrophotometry, Infrared , Structure-Activity Relationship , Urease/antagonists & inhibitors , Urease/metabolism
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