CAS NO: | 898537-18-3 |
生物活性 | Luseogliflozin (TS 071) is a potent, selective, orally activesodium-dependent glucose cotransporter (SGLT) 2inhibitor, with anIC50of 2.26 nM, about 1765-fold selectivity overSGLT1(IC50, 3990 nM). Luseogliflozin has the protential for treating type 2 diabetes. | ||
IC50& Target[1] |
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体外研究 (In Vitro) | Luseogliflozin (TS-071, 3p) is a potent sodium-dependent glucose cotransporter 2 (SGLT2) inhibitor, with an IC50of 2.26 nM, about 1765-fold selectivity over SGLT1 (IC50, 3990 nM); Luseogliflozin has the protential for treating type 2 diabetes[1]. | ||
体内研究 (In Vivo) | Luseogliflozin (1 mg/kg, p.o.) exhibits a blood glucose lowering effect, excellent urinary glucose excretion properties, and promising PK profiles in rats and dogs[1]. | ||
Clinical Trial | |||
分子量 | 434.55 | ||
Formula | C23H30O6S | ||
CAS 号 | 898537-18-3 | ||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||
储存方式 | Please store the product under the recommended conditions in the Certificate of Analysis. |
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