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PZ-1657 hydrochloride (Compound 57) 是一种口服活性的高效选择性5-羟色胺 7 受体 (5-HT7 receptor) 反向激动剂,其Ki值为5 nM。它能够抑制通过Gs信号通路介导的组成型cAMP生成,EC50值为2.93 nM。同样,它显著降低小鼠海马体中由5-HT7受体介导的MMP-9活性,效果相当于SB-269970。此外,PZ-1657 hydrochloride 能逆转苯环利定 (Phencyclidine) 诱导的大鼠新物体识别实验观察到的认知缺陷,而不影响其自发活动。该化合物适用于抑郁症和双相情感障碍等情感障碍的研究。
PZ-1657 hydrochloride (Compound 57) 是一种口服活性的高效选择性5-羟色胺 7 受体 (5-HT7 receptor) 反向激动剂,其Ki值为5 nM。它能够抑制通过Gs信号通路介导的组成型cAMP生成,EC50值为2.93 nM。同样,它显著降低小鼠海马体中由5-HT7受体介导的MMP-9活性,效果相当于SB-269970。此外,PZ-1657 hydrochloride 能逆转苯环利定 (Phencyclidine) 诱导的大鼠新物体识别实验观察到的认知缺陷,而不影响其自发活动。该化合物适用于抑郁症和双相情感障碍等情感障碍的研究。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 10 mg | 待询 | 待询 | |
| 50 mg | 待询 | 待询 |
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| 产品描述 | PZ-1657 hydrochloride (Compound 57) is a potent, selective, and orally active 5-HT7 receptor inverse agonist, with a Ki value of 5 nM. It inhibits constitutive cAMP production mediated by the Gs signaling pathway, with an EC50 value of 2.93 nM. PZ-1657 hydrochloride significantly reduces 5-HT7 receptor-mediated MMP-9 activity in the mouse hippocampus, showing effects comparable to SB-269970. It reverses cognitive deficits induced by phencyclidine in a rat novel object recognition test without affecting spontaneous activity. PZ-1657 hydrochloride is useful for researching affective disorders such as depression and bipolar disorder. |
| 靶点活性 | 5-HT7 receptor:5 nM (Ki) |
| 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 |
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