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GPR40 agonist 4

    级别和纯度:
  • 10mM in DMSO
  • CAS编号: 2102196-57-4
  • 分子式: C21H17ClO5S
  • 分子量: 416.87
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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
G655813-1ml
1ml 期货 Stock Image

基本描述

别名 GPR40 激动剂 4
规格或纯度 10mM in DMSO
英文名称 GPR40 agonist 4
生化机理 GPR40 激动剂 4 是一种强效的游离脂肪酸受体 1(FFA1/ GPR40)激动剂,pEC 50 为 7.54。
储存温度 -80℃储存
运输条件 超低温冰袋运输
作用类型 激动剂
产品介绍


GPR40 agonist 4 is a potent free fatty acid receptor 1 ( FFA1/ GPR40 ) agonist with a pEC 50 of 7.54.

In Vitro

GPR40 agonist 4 tends to have a low risk of activating caspase-3/7. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Single oral administration of GPR40 agonist 4 (compound 20) robustly reduces the plasma glucose excursion and enhances insulin secretion during an oral glucose tolerance test (OGTT) in a dose-dependent manner from 1 to 10 mg/kg when GPR40 agonist 4 is dosed 60 min prior to the oral glucose challenge. The area under the curve of blood glucose (AUC 0-120min ) and blood insulin (AUC 0-120min ) reveal that the minimum effective dose of GPR40 agonist 4 is 3 mg/kg. The hyperglycemia state is also markedly improved in GPR40 agonist 4 (20 mg/kg) treated group . MCE has not independently confirmed the accuracy of these methods. They are for reference only.

IC50& Target:pEC 50 : 7.54 (FFA1/GPR40)

关联靶点(人)

FFAR1 Tchem 游离脂肪酸受体1(Free fatty acid receptor 1) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)

名称和识别符

分子类型 小分子
Isomeric SMILES C1=CC=C(C(=C1)C2=CC=CC(=C2)COC3=CC=C(C=C3)S(=O)(=O)CC(=O)O)Cl
PubChem CID 131842087
分子量 416.87

质检证书(CoA,COO,BSE/TSE 和分析图谱)

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