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GPR120 Agonist 2 {[allProObj[0].p_purity_real_show]}

货号:A748720

GPR120 Agonist 2是一个 GPR120 激动剂,来自专利 US 20110313003 A1,实例 209。

GPR120 Agonist 2 化学结构 CAS号:1234844-11-1
GPR120 Agonist 2 化学结构
CAS号:1234844-11-1
GPR120 Agonist 2 3D分子结构
CAS号:1234844-11-1
GPR120 Agonist 2 化学结构 CAS号:1234844-11-1
GPR120 Agonist 2 3D分子结构 CAS号:1234844-11-1
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GPR120 Agonist 2 纯度/质量文件 产品仅供科研

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GPR120 Agonist 2 生物活性

描述 G protein-coupled receptor 120 (GPR120) is a Gαq coupled GPCR specifically activated by long-chain fatty acids (LCFAs). Upon stimulation by LCFAs, GPR120 can directly or indirectly modulate hormone secretion from the gastrointestinal tract and pancreas, and regulate lipid and/or glucose metabolism in adipose, liver, and muscle tissues. Additionally, GPR120 is postulated to mediate anti-inflammatory and insulin-sensitizing effects in adipose and macrophages[1]. GPR120 Agonist 2 is a GPR120 agonist which is useful for the treatment of metabolic diseases, including Type II diabetes and diseases associated with poor glycemic control. Agonism of GPR120 can reduce inflammation by inhibiting the expression of IL-6 and IL-8 induced by IL-1β[2]. GPR120 agonism correlates with prevention of the occurrence and development of metabolic disorders such as obesity and diabetes. GPR120 activation directly or indirectly inhibits inflammation, modulates hormone secretion from the gastrointestinal tract and pancreas, and regulates lipid and/or glucose metabolism in adipose, liver, and muscle tissues[3]. GPR120 agonist-treated wild-type, but not IL10-deficient and Blimp1-deficient, T helper type 1 cells induced less severe colitis. Furthermore, oral administration of GPR120 agonist protected mice from intestinal inflammation in both prevention and treatment schemes[4].

GPR120 Agonist 2 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT02444910 Diabetes Mellitus, Type 2 Phase 2 Completed - United States, Kentucky ... 展开 >> University of Kentucky's Center for Clinical and Translational Science (CCTS) Lexington, Kentucky, United States, 40536-0298 收起 <<
NCT03774095 Type 2 Diabetes Mellitus ... 展开 >> Obesity 收起 << Not Applicable Recruiting December 30, 2018 Denmark ... 展开 >> Odense University Hospital Recruiting Odense, Denmark, 5000 Contact: Karina Sørensen, MSc    26924602       Contact: Kurt Højlund, MD    +45 65413422 收起 <<

GPR120 Agonist 2 参考文献

[1] Xuqing Zhang, Mark J Macielag. GPR120 agonists for the treatment of diabetes: a patent review (2014 present).Expert Opin Ther Pat. 2020 Oct;30(10):729-742.

[2] Zhixian Xu,et al. Agonism of GPR120 prevented IL-1β-induced reduction of extracellular matrix through SOX-9. Aging (Albany NY). 2020 Jun 24;12(12):12074-12085.

[3]Dan Zhang, Po Sing Leung. Potential roles of GPR120 and its agonists in the management of diabetes.

[4]Wenjing Yang,et al. GPR120 Inhibits Colitis Through Regulation of CD4 + T Cell Interleukin 10 Production. Gastroenterology. 2021 Sep 16;S0016-5085(21)03497-1.

GPR120 Agonist 2 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.57mL

0.51mL

0.26mL

12.86mL

2.57mL

1.29mL

25.71mL

5.14mL

2.57mL

GPR120 Agonist 2 技术信息

CAS号1234844-11-1
分子式C22H25ClO4
分子量 388.885
别名
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Sealed in dry,Store in freezer, under -20°C

溶解方案

DMSO: 50 mg/mL(128.57 mM),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

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的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
方案一
方案二
动物实验配方
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