AH 7614
| 中文名称 | AH 7614 |
|---|---|
| 中文同义词 | 化合物AH 7614;AH-7614,FFA4 / GPR120拮抗剂 |
| 英文名称 | AH 7614 |
| 英文同义词 | AH 7614;4-Methyl-N-(9H-xanthen-9-yl)-benzenesulfonamide;Benzenesulfonamide, 4-methyl-N-9H-xanthen-9-yl-;allosteric,linoleic,negative,FFAR,GPR120,FFA4,inhibit,AH7614,AH-7614,NAM,Inhibitor,Free Fatty Acid Receptor,acid |
| CAS号 | 6326-06-3 |
| 分子式 | C20H17NO3S |
| 分子量 | 351.42 |
| EINECS号 | |
| 相关类别 | 抑制剂 |
| Mol文件 | 6326-06-3.mol |
| 结构式 |  |
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。 |
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.
安全信息
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2024/04/30 | HY-19996 | AH-7614 | 1 mg | 280元 | |
| 2024/04/30 | HY-19996 | AH 7614 AH-7614 | 6326-06-3 | 5mg | 700元 |