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CP94253 是一种口服有效的5-HT1B选择性激动剂,作用机制为通过与碘氰基吲哚洛尔 (ICP) 竞争性结合5-HT1受体。它与5-HT1B、5-HT1A、5-HT1D、5-HT1C和5-HT2受体结合,Ki值分别为2、89、49、860和1600 nM。在大鼠模型中,CP94253导致饱腹感、厌食、体重减轻和运动亢进。

CP94253 是一种口服有效的5-HT1B选择性激动剂,作用机制为通过与碘氰基吲哚洛尔 (ICP) 竞争性结合5-HT1受体。它与5-HT1B、5-HT1A、5-HT1D、5-HT1C和5-HT2受体结合,Ki值分别为2、89、49、860和1600 nM。在大鼠模型中,CP94253导致饱腹感、厌食、体重减轻和运动亢进。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 25 mg | ¥ 10,600 | 4-6周 | |
| 50 mg | ¥ 13,800 | 4-6周 | |
| 100 mg | ¥ 17,500 | 4-6周 |
CP94253 相关产品
| 产品描述 | CP94253 is an orally active selective agonist of the serotonin receptor 1B (5-HT1B), exhibiting agonistic activity by competitively binding to 5-HT1 receptors with iodocyanopindolol (ICP). It binds to the 5-HT1B, 5-HT1A, 5-HT1D, 5-HT1C, and 5-HT2 receptors with Ki values of 2, 89, 49, 860, and 1600 nM, respectively. In rat models, CP94253 induces satiety, anorexia, weight loss, and hyperactivity. |
| 靶点活性 | 5-HT2 receptor:1600 nM (Ki), 5-HT1D receptor:49 nM (Ki), 5-HT1A receptor:89 nM (Ki), 5-HT1C receptor:860 nM (Ki), 5-HT1B receptor:2 nM (Ki) |
| 分子量 | 257.33 |
| 分子式 | C15H19N3O |
| CAS No. | 131084-35-0 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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