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High affinity α7 nAChR partial agonist (Ki = 1.1 nM in rat; Emax < 10% of the response to ACh in rat and human). Inhibits ACh (IC50 = 2.7 nM) at α7 nAChR. Reduces LPS-induced TNF-α release from microglia enriched cultures. Anti-inflammatory.
High affinity α7 nAChR partial agonist (Ki = 1.1 nM in rat; Emax < 10% of the response to ACh in rat and human). Inhibits ACh (IC50 = 2.7 nM) at α7 nAChR. Reduces LPS-induced TNF-α release from microglia enriched cultures. Anti-inflammatory.

| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 50 mg | ¥ 7,945 | 待询 |
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| 产品描述 | High affinity α7 nAChR partial agonist (Ki = 1.1 nM in rat; Emax < 10% of the response to ACh in rat and human). Inhibits ACh (IC50 = 2.7 nM) at α7 nAChR. Reduces LPS-induced TNF-α release from microglia enriched cultures. Anti-inflammatory. |
| 分子量 | 400.83 |
| 分子式 | C19H20ClF3N2O2 |
| CAS No. | 753499-14-8 |
| Smiles | Cl.FC(F)(F)c1cccc(c1)-c1ccc(o1)C(=O)N1CCN2CCC1CC2 |TLB:16:18:22.23:25.26| |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. 实际储存温度请以COA为准 |
| 溶解度信息 | DMSO: Soluble |
对于不同动物的给药剂量换算,您也可以参考 更多