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Phenylboronic acid catalyzed synthesis of polysubstituted 1, 4-dihydropyridine derivatives as promising antioxidant agents correlated with molecular docking

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dc.contributor.author Pansuriya, Ketan
dc.contributor.author Lalpara, Jaydeep N.
dc.contributor.author Hadiyal, Sanjay D.
dc.contributor.author Dhaduk, Bhavin B.
dc.contributor.author Dubal, G.G.
dc.date.accessioned 2024-11-18T11:46:22Z
dc.date.available 2024-11-18T11:46:22Z
dc.date.issued 2022-12
dc.identifier.citation Pansuriya, K., Lalpara, J. N., Hadiyal, S. D., Dhaduk, B. B., & Dubal, G. G. (2022). Phenylboronic acid catalyzed synthesis of polysubstituted 1, 4-dihydropyridine derivatives as promising antioxidant agents correlated with molecular docking. Chemical Data Collections, 42, 100946 en_US
dc.identifier.uri http://10.9.150.37:8080/dspace//handle/atmiyauni/1651
dc.description.abstract A series of polysubstituted 1,4-dihydropyridines (4a-i) were designed and developed using Ph-B(OH)2 catalyst. Further, compounds were confirmed by various spectroscopic techniques. After that all compounds were studied for molecular docking against the human peroxidase enzyme (1PRX). Results of docking revealed that many compounds exhibited low binding score. To get a reference from the docking study, all synthesized molecules were evaluated for in vitro antioxidant assay using DPPH, H2O2 and NO methods. Most of the tested compounds exhibited good to moderate inhibition. Amongst, these compounds 4a (0.150, 0.141, 0.154 µM) and 4b (0.146, 0.134, 0.149 µM) possessed more significant activity than positive control ascorbic acid en_US
dc.language.iso en en_US
dc.publisher Elsevier / Chemical Data Collections en_US
dc.relation.ispartofseries ;42, 100946
dc.subject 1,4-dihydropyridine en_US
dc.subject Boronic acid catalysed en_US
dc.subject Antioxidants en_US
dc.subject Molecular docking en_US
dc.subject Hantzsch synthesis en_US
dc.title Phenylboronic acid catalyzed synthesis of polysubstituted 1, 4-dihydropyridine derivatives as promising antioxidant agents correlated with molecular docking en_US
dc.type Article en_US


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