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Synthesis, Characterization and Hypoglycemic Efficacy of Isonicotinohydrazide Phenoxy Quinolines: An in silico Studies
Corresponding Author(s) : V. Vijayakumar
Asian Journal of Chemistry,
Vol. 34 No. 9 (2022): Vol 34 Issue 9
Abstract
Prevention of α-amylase and β-glucosidase to reduce the postprandial blood sugar levels and delays dextrose absorption, the natural inhibitors provide an interesting approach to manage hyperglycemia with type 2 diabetes. The α-amylase and β-glucosidase are important therapeutic targets for type II diabetes. The isonicotinohydrazide phenoxy quinolines (5a-l) were synthesized and characterized by mass, 1H & 13C NMR. The characterized compounds are investigated for their in silico anti-hyperglycemic efficacy and the compounds shown effective to moderate inhibition against α-amylase and β-glucosidase enzymes. A molecular modelling study was performed for all the synthesized compounds to find the binding interaction of 5a-l with the α-amylase and β-glucosidase.
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A. Sharma, V. Kumar, R. Khare, G.K. Gupta and V. Beniwal, Med. Chem. Res., 24, 1830 (2015); https://doi.org/10.1007/s00044-014-1265-9
P.S. Sri Ramya, L. Guntuku, S. Angapelly, S. Karri, C.S. Digwal, B.N. Babu, V.G.M. Naidu and A. Kamal, Bioorg. Med. Chem. Lett., 28, 892 (2018); https://doi.org/10.1016/j.bmcl.2018.01.070
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