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L-902688 is an orally active EP4 receptor agonist (Ki: 0.38 nM; EC50: 0.6 nM). L-902688 displays >4,000-fold selective for EP4 over other EP and prostanoid receptors.

L-902688 is an orally active EP4 receptor agonist (Ki: 0.38 nM; EC50: 0.6 nM). L-902688 displays >4,000-fold selective for EP4 over other EP and prostanoid receptors.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 500 μg | ¥ 2,830 | 35日内发货 | |
| 1 mg | ¥ 5,370 | 35日内发货 | |
| 5 mg | ¥ 23,900 | 35日内发货 | |
| 10 mg | ¥ 41,800 | 35日内发货 |
| 产品描述 | L-902688 is an orally active EP4 receptor agonist (Ki: 0.38 nM; EC50: 0.6 nM). L-902688 displays >4,000-fold selective for EP4 over other EP and prostanoid receptors. |
| 靶点活性 | EP4:0.38 nM (ki), EP4:0.6 nM (EC50) |
| 体外活性 | L-902688 (1 μM; 24 hours; HUVE cells) treatment, decreases TGF-β-induced Twist and α-smooth muscle actin (α-SMA) expression. |
| 体内活性 | In the monocrotaline (MCT)-induced PAH rat model, L-902688 (0.25-1 μg/kg/day; intraperitoneal injection; daily; for 3 weeks; adult male Sprague-Dawley rats) treatment decreases right ventricle fibrosis [1]. |
| 分子量 | 419.47 |
| 分子式 | C21H27F2N5O2 |
| CAS No. | 634193-54-7 |
| Smiles | C(=C/[C@H](C(F)(F)C1=CC=CC=C1)O)\[C@@H]2N(CCCCCCC=3NN=NN3)C(=O)CC2 |
| 密度 | no data available |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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