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T-1095
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。
T-1095图片
CAS NO:209746-59-8

T-1095 是一种选择性和具有口服活性的 Na+-葡萄糖协同转运蛋白 (SGLT) 抑制剂,对人 SGLT1 和 SGLT2 的IC50分别为 22.8 μM 和 2.3 μM。T-1095 可用于糖尿病研究。
生物活性

T-1095 is a selective and orally activeNa+-glucose cotransporter (SGLT)inhibitor withIC50s of 22.8 μM and 2.3 μM for humanSGLT1andSGLT2, respectively. T-1095 can be used for diabetes research[1].

IC50& Target[1]

hSGLT1

22.8 μM (IC50)

hSGLT2

2.3 μM (IC50)

体内研究
(In Vivo)

T-1095 is absorbed into the circulation via oral administration, is metabolized to the active form, T-1095A, and suppresses the activity of SGLTs in the kidney[1].
Orally administered T-1095 (3-30 mg/kg) increases urinary glucose excretion in diabetic animals, thereby decreasing blood glucose levels[1].
With long-term T-1095 (0.01% or 0.1% T-1095 mixed diet; for 28 days) treatment, both blood glucose and HbA1c levels were reduced in streptozotocin (STZ)-induced diabetic rats and yellow KK mice. In addition, there was amelioration of abnormal carbohydrate metabolism, i.e., hyperinsulinemia and hypertriglyceridemia, and of the development of microalbuminuria, in yellow KK mice[1].

分子量

516.49

Formula

C26H28O11

CAS 号

209746-59-8

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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