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Ipragliflozin (L-Proline) {[allProObj[0].p_purity_real_show]}

货号:A245799 同义名: Ipragliflozin L-Proline

Ipragliflozin (L-Proline) selectively inhibits SGLT2 with IC50 of 2.8 nM.

Ipragliflozin (L-Proline) 化学结构 CAS号:951382-34-6
Ipragliflozin (L-Proline) 化学结构
CAS号:951382-34-6
Ipragliflozin (L-Proline) 3D分子结构
CAS号:951382-34-6
Ipragliflozin (L-Proline) 化学结构 CAS号:951382-34-6
Ipragliflozin (L-Proline) 3D分子结构 CAS号:951382-34-6
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Ipragliflozin (L-Proline) 纯度/质量文件 产品仅供科研

货号:A245799 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 SGLT1 SGLT2 其他靶点 纯度
Phloretin 98%
Canagliflozin +++

mSGLT2, IC50: 2 nM

hSGLT2, IC50: 3.7 nM

95%
Empagliflozin ++

SGLT2, IC50: 3.1 nM

98%
Dapagliflozin ++++

hSGLT2, EC50: 1.1 nM

97%
Tofogliflozin (hydrate) +++

hSGLT2, IC50: 2.9 nM

99%+
Sotagliflozin +

SGLT1, IC50: 36 nM

++++

SGLT2, IC50: 1.8 nM

98%
Ipragliflozin ++

hSGLT2, IC50: 7.4 nM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Ipragliflozin (L-Proline) 生物活性

描述 Ipragliflozin (L-Proline) potently and selectively inhibits human, rat, and mouse SGLT2 at nanomolar concentrations and exhibits stability against intestinal glucosidases[3].
体内研究

Ipragliflozin (L-Proline) displays favorable pharmacokinetic properties and dose-dependently increases urinary glucose excretion, lasting for over 12 hours in normal mice[3].

Oral administration of Ipragliflozin increases urinary glucose excretion in a dose-dependent manner, with significant effects observed at doses of 0.3 mg/kg or higher, and this effect persists for over 12 hours[4].

Single administration of Ipragliflozin dose-dependently increases urinary glucose excretion, reduces blood glucose and plasma insulin levels, and improves glucose intolerance[1].

体外研究

Ipragliflozin (L-Proline) potently and selectively inhibits human, rat, and mouse SGLT2 at nanomolar concentrations and exhibits stability against intestinal glucosidases[3].

Ipragliflozin (L-Proline) 参考文献

[1]Leibo Wang, et al. Optimization of NAMPT activators to achieve in vivo neuroprotective efficacy. Eur J Med Chem. 2022 Jun 5;236:114260.

[2]Tahara A, et al. Pharmacological profile of ipragliflozin (ASP1941), a novel selective SGLT2 inhibitor, in vitro and in vivo. Naunyn Schmiedebergs Arch Pharmacol. 2012 Apr;385(4):423-36.

[3]Tahara A, et al. Antidiabetic effects of SGLT2-selective inhibitor ipragliflozin in streptozotocin-nicotinamide-induced mildly diabetic mice. J Pharmacol Sci. 2012;120(1):36-44.

Ipragliflozin (L-Proline) 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.92mL

0.38mL

0.19mL

9.62mL

1.92mL

0.96mL

19.25mL

3.85mL

1.92mL

Ipragliflozin (L-Proline) 技术信息

CAS号951382-34-6
分子式C26H30FNO7S
分子量 519.582
别名 Ipragliflozin L-Proline
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Inert atmosphere,2-8°C

溶解度

DMSO: 18 mg/mL(34.64 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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