Article ID Journal Published Year Pages File Type
7796110 European Journal of Medicinal Chemistry 2018 39 Pages PDF
Abstract
A novel series of 6-amino-pyrido[2,3-d]pyrimidine-2,4-dione derivatives 3a-s were synthesized and evaluated as new inhibitors for α-glucosidase. All synthesized compounds were superior to standard drug (acarbose). Particularly, compound 3o was around 10-fold more potent than standard drug. The kinetic analysis of the compound 3o revealed that this compound inhibited α-glucosidase in a competitive manner (Ki = 69.2 μM). Docking studies of the most active compounds 3o, 3i, 3e, and 3m were also performed.112
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