Bevenopran (Synonyms: CB-5945; ADL-5945)
目录号: PL08081 纯度: ≥99%
CAS No. :676500-67-7
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中文名称
Bevenopran
中文别名
倍福普兰;5-(2-甲氧基-4-(((2-(四氢-2H-吡喃-4-基)乙基)氨基)甲基)苯氧基)吡嗪-2-甲酰胺
英文名称
Bevenopran
英文别名
5-[2-methoxy-4-[[2-(oxan-4-yl)ethylamino]methyl]phenoxy]pyrazine-2-carboxamide;5-(2-Methoxy-4-(((2-(tetrahydro-2H-pyran-4-yl)ethyl)amino)methyl)phenoxy)pyrazine-2-carboxamide;Bevenopran;IC58Q2EHPJ;2-PYRAZINECARBOXAMIDE, 5-[2-METHOXY-4-[[[2-(TETRAHYDRO-2H-PYRAN-4-YL)ETHYL]AMINO]METHYL]PHENOXY]-;Bevenopran [USAN:INN];Bevenopran (USAN/INN);ZGCYVRNZWGUXNQ-UHFFFAOYSA-N;CB5945;DB12464;SB16949;5-[2-methoxy-4-[[2-(oxan-4-yl)ethylamino]methyl]phenoxy]p
Cas No.
676500-67-7
分子式
C20H26N4O4
分子量
386.44
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Bevenopran 是一种外周 μ 阿片受体 (μ-opioid receptor) 拮抗剂。
生物活性
Bevenopran is a peripheral μ-opioid receptor antagonist.
性状
Solid
IC50 & Target[1][2]
μ-opioid receptor
体内研究(In Vivo)
Bevenopran is a peripheral μ-opioid receptor antagonist. Bevenopran is currently under investigation for the treatment of opioid-induced bowel dysfunction (OBD). Bevenopran tends to increase bowel movement (BM) frequency, especially for 0.1 mg twice daily and 4 mg daily, respectively. 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
ClinicalTrial
参考文献
[1]. Diego L, et al. Novel opioid antagonists for opioid-induced bowel dysfunction. Expert Opin Investig Drugs. 2011 Aug;20(8):1047-56.
[2]. Siemens W, et al. Advances in pharmacotherapy for opioid-induced constipation - a systematic review. Expert Opin Pharmacother. 2015 Mar;16(4):515-32.
溶解度数据
In Vitro: DMSO : 125 mg/mL (323.47 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

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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