Drug intelligence / Profile preview

glisoxepide

Development stage
Unknown
Modality
Small Molecules
Administration
Oral
01

Overview

Glisoxepide is a second-generation sulfonylurea oral antidiabetic drug used primarily for the management of type 2 diabetes mellitus. It acts as a hypoglycemic agent by stimulating insulin secretion from pancreatic beta cells through inhibition of ATP-sensitive potassium channel subunit Kir6.2/SUR1 complex (KATP) channels, leading to membrane depolarization, opening of voltage-gated calcium channels, and increased insulin release. Additionally, it may enhance peripheral insulin sensitivity and reduce serum glucagon levels. Glisoxepide also inhibits the uptake of bile acids into hepatocytes and is a specific inhibitor of the L-aspartate/L-glutamate antiport system[1][2][5][6].

Brand names
GlipiridePro-diaban
Other names
glisoxepid4-(4-beta-(5-methylisoxazol-3-carboxamidoethyl)phenylsulfonyl)-1,1-hexamethylenesemicarbazide
02

Targets

SUR1 (Sulfonylurea receptor 1)KCNJ11 (Atp-sensitive inward rectifier potassium channel 11)

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