Abstract α-Glucosidase is an important therapeutic target of diabetes mellitus. To find potent
α-glucosidase inhibitors, thirty-one β-carboline derivatives containing piperazine moieties …

In this study, we designed and synthesized a novel class of 1, 3, 4-oxadiazolyl-containing β-
carboline derivatives, ie, compounds f1∼ f35 as potential α-glucosidase inhibitors. All the …

Abstract A new series of 1, 2, 4-triazine derivatives bearing carbazole moiety 7a–7p were
designed, synthesized, and evaluated for their α-glucosidase inhibitory activity. The majority …

To find potential α-glucosidase inhibitors, indolo [1, 2-b] isoquinoline derivatives (1–20)
were screened for their α-glucosidase inhibitory effects. All derivatives presented potential α …

A series of novel pyrazole-phenyl semicarbazone derivatives were designed, synthesized,
and screened for in vitro α-glucosidase inhibitory activity. Given the importance of hydrogen …

In order to find new α-glucosidase inhibitors with high efficiency and low toxicity, novel
chromone-based benzohydrazide derivatives 6a-6s were synthesized and characterized …

A series of chromone derivatives were designed, synthesized, and evaluated for their α-
glucosidase inhibitory activity by using in vitro methods and molecular docking studies …

In this study, twenty novel cinnamic acid magnolol derivatives were synthesized, and
screened for their anti-hyperglycemic potential. All synthesized compounds exhibited good …

To discover potent α-glucosidase inhibitors, a class of novel triazole-phenylacetamide
derivatives (5a-5p) were designed, prepared, and tested for their α-glucosidase inhibitory …

To develop novel α-glucosidase inhibitors, a series of chromone-based phenylhydrazone
and benzoylhydrazone derivatives were designed, synthesized, and evaluated their …