Bexagliflozin CAS# 1118567-05-7 贝沙格列净
Bexagliflozin is a potent, selective SGLT2 inhibitor designed to reduce renal glucose reabsorption. In preclinical enzyme assays, it showed high affinity for human SGLT2 (IC₅₀ ~1–2 nM) with >300-fold selectivity over SGLT1. In rodent models of diabetes, oral bexagliflozin produced robust glucosuria and lowered fasting glucose by 25–40%, with parallel reductions in HbA1c after repeated dosing. It also improved insulin sensitivity and reduced body-weight gain in diet-induced obese animals. Toxicology studies in rats and dogs indicated good tolerability and a safety profile consistent with other SGLT2 inhibitors.
📌 参考资料/链接:
C-Aryl glucosides substituted at the 4'-position as potent and selective renal sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors for the treatment of type 2 diabetesBy: Xu, Baihua; et alBioorganic & Medicinal Chemistry Letters (2011), 21(15), 4465-4470
📄 详细内容
CAS No. 1118567-05-7 贝沙格列净Bexagliflozin synthetic routes

C-Aryl glucosides substituted at the 4'-position as potent and selective renal sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors for the treatment of type 2 diabetesBy: Xu, Baihua; et alBioorganic & Medicinal Chemistry Letters (2011), 21(15), 4465-4470
产品链接: CAS No. 1118567-05-7 ››