AH 7614
AH 7614 性质
熔点 | 196-197 °C(Solv: ethanol (64-17-5); 1,4-dioxane (123-91-1)) |
---|---|
沸点 | 505.9±60.0 °C(Predicted) |
密度 | 1.37±0.1 g/cm3(Predicted) |
储存条件 | -20°C (des.) |
溶解度 | 溶于DMSO(最高50mg/ml)或乙醇(升温最高8mg/ml)。 |
形态 | 固体 |
酸度系数(pKa) | 10.33±0.20(Predicted) |
颜色 | 米白色 |
稳定性 | 可在-20°下的DMSO或乙醇溶液保存长达1个月。 |
AH 7614 用途与合成方法
pIC50: 7.1 (human FFA4)
AH-7614 (compound 39) (0.063-1 μM) blocks intracellular Ca
2+
response induced by both linoleic acid and FFAR4 agonist in FFA4 expressing U2OS cells.
AH-7614 (100 μM) abolishes the enhancement in glucose-stimulated insulin secretion by GSK137647A in NCI-H716 cells.
AH-7614 (0.001-10 μM; 15 min) blocks TUG-891-mediated internalization of FFA4 from the cell surface (pIC
50
=7.70).
AH-7614 (10 μM; 30 min) blocks agonist-induced elevation of intracellular inositol monophosphates and phosphorylation of FFA4.
AH7614 (50 μg; intratumoral injection once every 4 d for 20 d) reduces the tumor growth in mice.
AH7614 (50 μg; intratumoral injection one day prior to epirubicin injection) enhances cancer cell sensitivity to the chemotherapy and inhibit tumor progression by blocking GPR120 signaling in combination with Epirubicin.
AH 7614 价格(试剂级)
更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
---|---|---|---|---|---|
2024-11-08 | HY-19996 | 1 mg | 280 | ||
2024-11-08 | HY-19996 | AH 7614 | 6326-06-3 | 5mg | 700 |