|Elimination half-life||1.5 hours|
|CompTox Dashboard (EPA)|
|Chemical and physical data|
|Molar mass||317.423 g/mol g·mol−1|
|3D model (JSmol)|
|(what is this?)|
Nateglinide belongs to the meglitinide class of blood glucose-lowering drugs.
Nateglinide lowers blood glucose by stimulating the release of insulin from the pancreas. It achieves this by closing ATP-dependent potassium channels in the membrane of the β cells. This depolarizes the β cells and causes voltage-gated calcium channels to open. The resulting calcium influx induces fusion of insulin-containing vesicles with the cell membrane, and insulin secretion occurs.
Nateglinide is contraindicated in patients who:
A study funded by Novo Nordisk, the U.S. distributor for Repaglinide, compared their product with Nateglinide in "A randomized, parallel-group, open-label, multicenter 16-week clinical trial". They concluded that the two were similar, but "repaglinide monotherapy was significantly more effective than nateglinide monotherapy in reducing HbA1c and FPG values after 16 weeks of therapy."
Nateglinide is delivered in 60 mg & 120 mg tablet form.