alexa Molecular Docking, Synthesis And Anticonvulsant Activity Study Of Some Novel Hydrazone Derivatives
ISSN: 2169-0138

Drug Designing: Open Access
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4th Annual Congress on Drug Discovery & Designing
July 03-04, 2017 Bangkok, Thailand

Arvind Kumar
S D College of Pharmacy & Vocational Studies, India
Posters & Accepted Abstracts: Drug Des
DOI: 10.4172/2169-0138-C1-014
Abstract
Series of 4-(4-Ethyl-phenyl)-4-oxo-butyric acid (1-substituted phenyl)-hydrazide and 2-[5-(substituted-phenyl)-5-methyl- 4,5-dihydro-[1,3,4]oxadiazole-2-yl)-1-(4-ethyl-phenyl)-ethanone have been synthesized and characterized by NMR, IR, Mass and C, H, N analysis. The docking studies of novel substituted hydrazones and 1,3,4-oxadiazole derivatives have been performed with the AutoDock Vina PyRx-Python Prescription 0.8 in to the 3D structure of the catalytic site of human gammaaminobutyric acid receptor (PDB ID: 4COF). Best compounds selected on the basis of least binding energies for receptor 4COF among all compounds, H-9, 10, 22, 26 shows least mean binding energy -7.4, -7.0, -7.4 and -7.2 respectively. All these four compounds were evaluated for anticonvulsant activity using maximum electroshock seizures (MES) in male Wister rats (180-220 g). Compounds H-9 shows significant anticonvulsant activity.
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