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Chemoenzymatic and Protecting-Group-Free Synthesis of 1,4-Substituted 1,2,3-Triazole-α-<scp>d</scp>-glucosides with Potent Inhibitory Activity toward Lysosomal α-Glucosidase

Jaggaiah N. Gorantla, Maniganda Santhi, Salila Pengthaisong, Lukana Ngiwsara, Phannee Sawangareetrakul, Suwadee Chokchaisiri, Prasat Kittakoop, Jisnuson Svasti, James R. Ketudat Cairns

2021ACS Omega12 citationsDOIOpen Access PDF

Abstract

more than 60-fold lower than that of the commercial α-glucosidase inhibitor acarbose.

Topics & Concepts

ChemistryAzideSodium azideClick chemistryStereochemistryGlucosideProtecting groupArylAmideOrganic chemistryAlternative medicineAlkylMedicinePathologyCarbohydrate Chemistry and SynthesisClick Chemistry and ApplicationsTransgenic Plants and Applications
Chemoenzymatic and Protecting-Group-Free Synthesis of 1,4-Substituted 1,2,3-Triazole-α-<scp>d</scp>-glucosides with Potent Inhibitory Activity toward Lysosomal α-Glucosidase | Litcius