Bamocaftor
目录号: PL02823 纯度: ≥99%
CAS No. :2204245-48-5
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中文名称
Bamocaftor
英文名称
Bamocaftor
英文别名
Bamocaftor;VX659;8C7XEW3K7S;Bamocaftor (USAN);Bamocaftor [USAN];VX 659 pound>>VX659;GTPL10553;BCP29456;WHO 11167;DB15177;compound 1 [WO2018064632A1];(S)-N-(phenylsulfonyl)-6-(3-(2-(1-(trifluoromethyl)cyclopropyl)ethoxy)-1H-pyrazol-1-yl)-2-(2,2,4-trimethylpyrrolidin-1-yl)nicotinamide;D11535;3-Pyridinecarboxamide, N-(phenylsulfonyl)-6-(3-(2-(1-(trifluoromethyl)cyclopropyl)ethoxy)-1H-pyrazol-1-yl)-2-((4S)-2,2,4-trimethyl-1-p
Cas No.
2204245-48-5
分子式
C28H32F3N5O4S
分子量
591.65
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Bamocaftor (VX-659) 是囊性纤维化跨膜电导调节 (CFTR) 校正器,被设计用于恢复 F508del-CFTR 蛋白功能。Bamocaftor 可与 Tezacaftor 和 Ivacaftor 一起用于囊性纤维化研究。
生物活性
Bamocaftor (VX-659) is a cystic fibrosis transmembrane conductance regulator (CFTR) corrector designed to restore F508del-CFTR protein function. Bamocaftor can be used combine with Tezacaftor and Ivacaftor in cystic fibrosis research.
性状
Solid
体外研究(In Vitro)
Bamocaftor is a CFTR corrector designed to restore F508del-CFTR protein function. 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]. Ghelani DP, et al. Emerging Cystic Fibrosis Transmembrane Conductance Regulator Modulators as New Drugs for Cystic Fibrosis: A Portrait of in Vitro Pharmacology and Clinical Translation.
溶解度数据
In Vitro: DMSO : 100 mg/mL (169.02 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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