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Mizagliflozin
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。
Mizagliflozin图片
规格:98%
分子量:564.67
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议

产品介绍
Mizagliflozin (DSP-3235 free base) 是一种高效、口服、选择性的 SGLT1 抑制剂,对人 SGLT1 的 Ki 值为 27 nM。Mizagliflozin 的对 SGLT1 选择性是 SGLT2 的 303 倍。Mizagliflozin 是一种抗糖尿病药物,可以改善餐后血糖波动。Mizagliflozin 在改善慢性便秘方面具有潜在的作用。
货号:ajcx29510
CAS:666843-10-3
分子式:C28H44N4O8
分子量:564.67
溶解度:Methanol: 250 mg/mL (442.74 mM); DMSO: 100 mg/mL (177.09 mM)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Mizagliflozin (DSP-3235 free base) is a potent, orally active and selective SGLT1 inhibitor, with a Ki of 27 nM for human SGLT1. Mizagliflozin displays 303-fold selectivity over SGLT2. Mizagliflozin is used as an antidiabetic drug that can modify postprandial blood glucose excursion. Mizagliflozin also exhibits potential in the amelioration of chronic constipation[1].


Mizagliflozin (DSP-3235 free base) (3-30 mg/kg; oral) exerts a laxative effect[1].Mizagliflozin administrated intravenously (0.3 mg/kg) and orally (3 mg/kg) declined with a short half-life (0.23 and 1.14 h, respectively)[2] Animal Model: Male Wistar rats (rat model of low-fiber-diet-induced constipation)[1]

[1]. Inoue T, et al. Mizagliflozin, a novel selective SGLT1 inhibitor, exhibits potential in the amelioration of chronic constipation. Eur J Pharmacol. 2017 Jul 5;806:25-31. [2]. Ohno H, et al. Absorption, disposition, metabolism and excretion of [14C]mizagliflozin, a novel selective SGLT1 inhibitor, in rats. Xenobiotica. 2019 Apr;49(4):463-473.