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twenty μM, respectively. Kinetic experiments exposed compound 142 acted to be a aggressive inhibitor of α-amylase along with a non-competitive inhibitor of α-glucosidase. Molecular docking scientific tests confirmed robust interactions amongst compound 142 and critical residues in the Lively web sites of both equally enzymes. The review also demonstrated that compound 142 remained secure within the enzyme binding web pages throughout molecular dynamics simulations, supporting its likely like a therapeutic agent for diabetes.
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