{Reference Type}: Journal Article
{Title}: Synthesis, in vitro [Formula: see text]-glucosidase inhibitory activity, and in silico study of (E)-thiosemicarbazones and (E)-2-(2-(arylmethylene)hydrazinyl)-4-arylthiazole derivatives.
{Author}: Ali M;Khan KM;Salar U;Ashraf M;Taha M;Wadood A;Hamid S;Riaz M;Ali B;Shamim S;Ali F;Perveen S;
{Journal}: Mol Divers
{Volume}: 22
{Issue}: 4
{Year}: Nov 2018
{Factor}: 3.364
{DOI}: 10.1007/s11030-018-9835-2
{Abstract}: This study is focused on the identification of thiazole-based inhibitors for the [Formula: see text]-glucosidase enzyme. For that purpose, (E)-2-(2-(arylmethylene)hydrazinyl)-4-arylthiazole derivatives were synthesized in two steps and characterized by various spectroscopic techniques. All derivatives and intermediates were evaluated for their in vitro [Formula: see text]-glucosidase inhibitory activity. Thiosemicarbazones 20 and 35, and cyclized thiazole derivatives 2, 5-11, 13, 15, 21-24, 27-31, and 36-37 showed significant inhibitory potential in the range of [Formula: see text]-[Formula: see text] as compared to standard acarbose ([Formula: see text]). A molecular modeling study was carried out to understand the binding interactions of compounds with the active site of enzyme.