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Purpurin and its analog R162 disrupt the redox homeostasis of cancer cells by inhibiting GLUD

17 Saxagliptin is a reversible, potent inhibitor that is selective for DPP-4 by more than 4,000-fold, compared with sitagliptin, whose selectivity is more than 2,600-fold

In addition, it is necessary to study data on the toxicity of WG on the liver in order to confirm the potential of WG for clinical application

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The Insulin Response to Oral Glucose in GIP and GLP-1 Receptor Knockout Mice: Review of the Literature and Stepwise Glucose Dose Response Studies in Female Mice

This impairment hinders -cell functional maturation and insulin release [232]