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Luseogliflozin
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Luseogliflozin图片
CAS NO:898537-18-3

TS 071
Luseogliflozin (TS 071) 是一种有效的、选择性的、具有口服活性的钠-葡萄糖协同转运蛋白 2 (SGLT2) 抑制剂,IC50值为 2.26 nM,对其选择性是对 SGLT1 的约 1765 倍 (IC50, 3990 nM)。Luseogliflozin 有治疗糖尿病的潜力。
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]

SGLT2

2.26 nM (IC50)

SGLT1

3990 nM (IC50)

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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