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Sitagliptin phosphate monohydrate
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。
Sitagliptin phosphate monohydrate图片
CAS NO:654671-77-9
包装与价格:
包装价格(元)
10 mM * 1 mL in Water电议
100mg电议
200mg电议
500mg电议
1 g电议

产品名称
西他列汀磷酸盐一水合物
MK-0431 phosphate monohydrate
产品介绍
Sitagliptin (MK0431 phosphate monohydrate) 是一种有效的DPP4抑制剂,在 Caco-2 细胞中,IC50值为 19 nM。
生物活性

Sitagliptin phosphate monohydrate (MK-0431 phosphate monohydrate) is a potent inhibitor ofDPP4with anIC50of 19 nM in Caco-2 cell extracts[1].

IC50& Target

IC50: 19 nM (DPP4, in Caco-2 cell extracts)

体外研究
(In Vitro)

Sitagliptin phosphate exhibits a potent inhibitory effect on DPP-4 with IC50of 19 nM from Caco-2 cell extracts[1]. Sitagliptin reduces in vitro migration of isolated splenic CD4 T-cells through a pathway involving cAMP/PKA/Rac1 activation[2]. A recent study demonstrates that sitagliptin exerts a novel, direct action in order to stimulate GLP-1 secretion by the intestinal L cell through a DPP-4-independent, protein kinase A- and MEK-ERK1/2-dependent pathway. It therefore reduces the effect of autoimmunity on graft survival[3].

体内研究
(In Vivo)

In vivo, the ED50value of sitagliptin phosphate for inhibition of plasma DPP-4 activity is calculated to be 2.3 mg/kg 7 hour postdose and 30 mg/kg 24 hour postdose in freely fed Han-Wistar rats[1]. The streptozotocin-induced type 1 diabetes mouse model exhibits elevated DPP-4 levels in the plasma that can be substantially inhibited in mice on an Sitagliptin phosphate diet. This is achieved by a positive effect on the regulation of hyperglycemia, potentially through prolongation of islet graft survival[4]. The plasma clearance and volume of distribution of Sitagliptin phosphate are higher in rats (40-48 mL/min/kg, 7-9 L/kg) than in dogs (9 mL/min/kg, 3 L/kg); and its half-life is shorter in rats,2 hours compared with 4 hours in dogs[5].

Clinical Trial
分子量

523.32

性状

Solid

Formula

C16H20F6N5O6P

CAS 号

654671-77-9

中文名称

磷酸西他列汀一水合物

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

H2O : ≥ 33 mg/mL(63.06 mM)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.9109 mL9.5544 mL19.1088 mL
5 mM0.3822 mL1.9109 mL3.8218 mL
10 mM0.1911 mL0.9554 mL1.9109 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (sealed storage, away from moisture)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: PBS

    Solubility: 50 mg/mL (95.54 mM); Clear solution; Need ultrasonic

*以上所有助溶剂都可在本网站选购。