GSK137647A

CAS号

349085-82-1

分子式

C16H19NO3S

主要靶点

GPR

仅限科研使用

Cat No : CM04295

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Synonyms

Inhibitor|insulin secretion|anti-inflammatory|inhibit|epithelial ion transport|FFA2|FFA4|FFAR|FFA3|FFA1|Free Fatty Acid Receptor|GSK 137647|GSK137647|GSK-137647|GSK137647A|GSK-137647A|GPR120



产品信息

CAS号 349085-82-1
分子式 C16H19NO3S
主要靶点 GPR
主要通路 G 蛋白偶联受体|内分泌与激素
分子量 305.39
纯度 99.87%, 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
别名 Inhibitor|insulin secretion|anti-inflammatory|inhibit|epithelial ion transport|FFA2|FFA4|FFAR|FFA3|FFA1|Free Fatty Acid Receptor|GSK 137647|GSK137647|GSK-137647|GSK137647A|GSK-137647A|GPR120

溶解度

DMSO:50 mg/mL (163.73 mM);H2O:< 0.06 mg/mL (insoluble or slightly soluble)

参考文献

1.Sparks SM. Etal. Bioorg Med Chem Lett. 2014 Jul 15;24(14):3100-3.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
=
×
×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
×
=
×
C1   V1   C2   V2