4-氨基-5-氯-N-(1-(3-甲氧基丙基)哌啶-4-基)-2,3-二氢苯并呋喃-7-甲酰胺琥珀酸盐
更新时间：2024-07-15 12:32:58
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| 常用名 | 琥珀酸普卡必利 | CAS号 | 179474-85-2 |
|---|---|---|---|
| 价格 | 纯度 | 99.0% | |
| 备货期 | 10天 | 库存 | 现货 |
| 产品详情（用途，包装等）
用途： Prucalopride succinate is a selective, high affinity 5-HT4 receptor agonist with pKi of 8.6/8.1 for 5-HT4a/4b.IC50 value:Target: 5-HT4 agonistin vitro: Prucalopride was a 5-HT(4) receptor agonist in the guinea-pig colon, as it induced contractions (pEC(50)=7.48+/-0.06; insensitive to a 5-HT(2A) or 5-HT(3) receptor antagonist, but inhibited by a 5-HT(4) receptor antagonist) as well as the facilitation of electrical stimulation-induced noncholinergic contractions (blocked by a 5-HT(4) receptor antagonist). Prucalopride did not cause relevant inhibition of 5-HT(2A), 5-HT(2B), or 5-HT(3), motilin or cholecystokinin (CCK(1)) receptor-mediated contractions, nor nicotinic or muscarinic acetylcholine receptor-mediated contractions, up to 10 microM [1].in vivo: Rat microdialysis studies revealed that prucalopride maximally increased ACh and histamine levels in the prefrontal cortex at 5 and 10 mg/kg, whereas PRX-03140 significantly increased cortical histamine levels at 50 mg/kg, failing to affect ACh release at doses lower than 150 mg/kg [2]. 物理化学性质： CAS号：179474-85-2 常用中文名：琥珀酸普卡必利 常用英文名：Prucalopride Succinate 分子式：C22H32ClN3O7 分子量：485.958 密度：N/A 沸点：N/A 熔点：N/A 闪点：N/A 储存条件：-20℃ |
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- 产品名：琥珀酸普卡比利
- 价格： ￥144.9/250mg ￥308.9/1g ￥1029.9/5g ￥需询单/250g
- 纯度：99.0%
- 备货期：1天
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参考价格：$106/10mM*1mLinDMSO