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Original Research Article | OPEN ACCESS

Synthesis of some pyridazine derivatives as antioxidants and antimicrobial agents

Abida 1 , Anupama Diwan1, Hamdy K Thabet2, Mohd Imran3

1School of Pharmaceutical Sciences, Apeejay Stya University, Sohna - Palwal Road, Sohna–122103, India; 2Department of Chemistry, Faculty of Science; 3Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Northern Border University, Rafha 91911, PO Box 840, Saudi Arabia.

For correspondence:-  Abida   Email: abida.mohd@asu.apeejay.edu   Tel:+918053027613

Accepted: 15 November 2019        Published: 31 December 2019

Citation: A, Diwan A, Thabet HK, Imran M. Synthesis of some pyridazine derivatives as antioxidants and antimicrobial agents. Trop J Pharm Res 2019; 18(12):2633-2641 doi: 10.4314/tjpr.v18i12.24

© 2019 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To prepare some pyridazine derivatives as antioxidant and antimicrobial agents.
Methods: The coupling of aryl diazonium salts with diethyl 2-cyano-3-methylglutaconate afforded pyridazine-5-carbonitrile derivatives (3a-e). The methyl function in the pyridazine derivatives (3a-e) reacted with cinnamonitriles to yield phthalazine derivatives (6a-h). Imino-pyridazine derivatives (9a-h) were obtained by reacting 2-aminoprop-1-ene-1,1,3-tricarbonitrile along with aryl diazonium salts (1a-h). Structure elucidation was done by spectral analysis. The 1,1-diphenyl-2-picryl hydrazyl (DPPH) technique was employed to assess antioxidant effect, while evaluation of antimicrobial activity was carried out by serial dilution technique.
Results: Compounds, 6f (IC50 = 12.68 μg/mL; p < 0.05), 6a (IC50 = 14.23 μg/mL; p < 0.05), and 3c (IC50 = 14.34 μg/mL; p < 0.05) displayed good antioxidant activity compared to ascorbic acid (IC50 = 12.45 μg/mL; p < 0.05). Based on the zone of inhibition, compound 6c (p < 0.05) displayed higher activity than ofloxacin (p < 0.05) against E. coli.
Conclusion: The presence of an oxo group and carboxylate group plays an important role in the antioxidant activity of these compounds. Compounds 6a, 6f, and 3c can potentially serve as lead compounds for the development of promising antioxidants.

Keywords: Pyridazine, Benzofused pyridazine, Antioxidant, Antimicrobial

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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