ArticleChemistry & biodiversity2026
An Exploration of the Antidiabetic Potential of 2-Thio-4-quinazolinone Scaffolds Using In Vitro and In Silico Approaches.
Article in Chemistry & biodiversity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Diabetes, a complicated metabolic disease, upsets glucose regulation and disturbs multiple organs, often resulting in problems like neuropathy and cardiovascular diseases. There is a pressing need to develop effective antidiabetic agents capable of managing glucose metabolism without compromising vital physiological functions. This study highlights the synthesis of 2-thio-4-quinazolinones (5a-j), the base-catalyzed intramolecular cyclization of corresponding 2-fluorobenzoyl-3-aryl thioureas (4a-j), and their exploration for α- and β-glucosidase inhibition. All the synthesized compounds exhibited strong α- and β-glucosidase inhibition, with compound 5a, containing chloro and nitro substituents, showing the most potent α-glucosidase inhibition with an IC
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