Journal
CHEMICAL PAPERS
Volume 74, Issue 12, Pages 4379-4388Publisher
SPRINGER INTERNATIONAL PUBLISHING AG
DOI: 10.1007/s11696-020-01246-7
Keywords
alpha-Glucosidase; Docking study; Kinetic study; Phthalimide; Schiff base; Coumarin
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We have designed and synthesized phthalimide-Schiff base-coumarin hybrids8a-b,9a-d,10a-b, and11a-dand evaluated them for alpha-glucosidase inhibitory potential against yeast form of this enzyme. For the synthesis of title compounds 4-hydroxybenzaldehyde, 4-hydroxy-3-methoxybenzaldehyde, 2-hydroxybenzaldehyde, 2-hydroxybenzaldehyde derivatives, coumarin-3-carbohydrazide, and coumarin-7-yloxy-acetohydrazide were used. In vitro alpha-glucosidase inhibition revealed that all the synthesized compounds exhibited outstanding alpha-glucosidase inhibition with IC50 values ranging between 85.2 +/- 1.7 and 577.7 +/- 7.5 mu M when compared with the standard inhibitor acarbose having IC50 value 750.0 +/- 12.0 mu M. The most potent compounds were 4-hydroxybenzaldehyde derivative 8 a with coumarin-3-carbohydrazide moiety, 2-hydroxy-5-nitrobenzaldehyde derivative 11d with coumarin-7-yl-oxy-acetohydrazide moiety, and 2-hydroxy-5-nitrobenzaldehyde derivative 9d with coumarin-3-carbohydrazide moiety. Molecular docking studies were carried out to understand the interaction modes and binding energies of the most active compounds and standard drug acarbose. This studies predicted that compounds8a,11d, and9d(respectively with binding energies = - 10.77, - 8.65, and - 8.66 kcal/mol) bind to active site alpha-glucosidase more easily than acarbose (binding energy = - 4.04 kcal/mol).
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