Revexepride
目录号: PL06140 纯度: ≥99%
CAS No. :219984-49-3
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中文名称
Revexepride
英文名称
Revexepride
英文别名
4-amino-5-chloro-N-[[(3S,4S)-3-hydroxy-1-(3-methoxypropyl)piperidin-4-yl]methyl]-2,2-dimethyl-3H-1-benzofuran-7-carboxamide;Revexepride;8C63R2Y02M;4-amino-5-chloro-N-(((3S,4S)-3-hydroxy-1-(3-methoxypropyl)piperidin-4-yl)methyl)-2,2-dimethyl-2,3-dihydrobenzofuran-7-carboxamide;Revexepride [INN];SB18754;R149402;Q27270174;SPD557
Cas No.
219984-49-3
分子式
C21H32ClN3O4
分子量
425.95
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Revexepride 是一种高度选择性的 5-HT4 receptor 激动剂,也是潜在的 CYP3A4 enzyme 诱导剂,可用于研究胃食管返流疾病。
生物活性
Revexepride is a highly selective 5-HT4 receptor agonist, and a potential inducer of CYP3A4 enzyme, used for the treatment of gastroesophageal reflux disease.
性状
Solid
IC50 & Target[1][2]
5-HT4 Receptor CYP3A4
体外研究(In Vitro)
The human CYP isoenzymes are involved in the metabolism of revexepride, which is mainly metabolized in vitro in humans by CYP3A4 (99.9%) with a minor contribution of CYP2D6 (0.1%). Revexepride exhibits direct inhibition of human CYP3A4 in vitro with IC50 values of 16-49 μM. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. David Pierce, et al. A phase 1 randomized study evaluating the effect of omeprazole on the pharmacokinetics of a novel 5-hydroxytryptamine receptor 4 agonist, revexepride (SSP-002358), in healthy adults. Drug Des Devel Ther. 2015; 9: 1257-1268.
溶解度数据
In Vitro: DMSO : ≥ 100 mg/mL (234.77 mM)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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