Nav1.7-IN-2

目录号: PL11347 纯度: ≥99%
Nav1.7-IN-2是电压门控钠通道抑制剂, 尤其是 Nav 1.7, IC50值为80 nM。
CAS No. :1332295-35-8
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中文名称
Nav1.7-IN-2
中文别名
Nav1.7-IN-2
英文名称
Nav1.7-IN-2
英文别名
Nav1.7-IN-2;Benzamide, 3-[[4-[3-(4-fluoro-2-methylphenoxy)-1-azetidinyl]-2-pyrimidinyl]amino]-N-methyl-;BDBM229646;BDBM229674;US9334269, J;US9334269, 1
Cas No.
1332295-35-8
分子式
C22H22FN5O2
分子量
407.44
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述
Nav1.7-IN-2是电压门控钠通道抑制剂, 尤其是 Nav 1.7, IC50值为80 nM。
产品详情
Nav1.7-IN-2是电压门控钠通道抑制剂, 尤其是 Nav 1.7, IC50值为80 nM。
生物活性
Nav1.7-IN-2 is an inhibitor of voltage-gated sodium channels (Nav), in particular Nav 1.7, with IC50 of 80 nM. IC50 value: 80 nM Target: Nav 1.7 Nav1.7-IN-2 is useful for the treatment of diseases treatable by inhibition of these channels, in particular, chronic pain disorder. The more detailed information please refer to WO 2011103196 A1. Nav1.7-IN-2 is a Nav1.7 channel inhibitor extracted from patent WO/2011103196 A1, compound example J, has an IC50 of 80 nM.
性状
Solid
IC50 & Target[1][2]
Nav1.7 80 nM (IC50)
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]. Bregman Howard, et al. Preparation of aryl carboxamide derivatives as sodium channel inhibitors for treatment of pain. From PCT Int. Appl. (2011), WO 2011103196 A1 20110825.
溶解度数据
In Vitro: DMSO : 50 mg/mL (122.72 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)
[1]. Bregman Howard, et al. Preparation of aryl carboxamide derivatives as sodium channel inhibitors for treatment of pain. From PCT Int. Appl. (2011), WO 2011103196 A1 20110825.

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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