AMG8379

目录号: GC39696纯度: >98%

AMG8379 是一种有效的、口服的、选择性的、电压门控钠通道 NaV1.7 拮抗剂, 对人和小鼠 NaV1.7 的 IC50 值分别为 8.5 和 18.6 nM。AMG8379 能可逆地阻断背根神经节 (DRG) 神经元内源性河豚毒素 (TTX) 敏感钠通道, IC50为 3.1 nM。


AMG8379
Cas No.: 1642112-31-9
规格价格库存数量操作
100mg¥4,320.00现货
1
250mg¥7,020.00现货
1
500mg¥19,800.00现货
1

文献被引

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产品描述 Description

AMG8379 is a potent, orally active and selective sulfonamide antagonist of the voltage-gated sodium channel NaV1.7, with IC50s of 8.5 and 18.6 nM for hNaV1.7 and mNaV1.7, respectively. AMG8379 potently and reversibly blocks endogenous Tetrodotoxin (TTX)-sensitive sodium channels in dorsal root ganglia (DRG) neurons with an IC50 of 3.1 nM[1].

[1]. Kornecook TJ, et al. Pharmacologic Characterization of AMG8379, a Potent and Selective Small Molecule Sulfonamide Antagonist of the Voltage-Gated Sodium Channel NaV1.7. J Pharmacol Exp Ther. 2017 Jul;362(1):146-160.

产品文档 Product Documents

化学性质Chemical Properties

CAS 号
1642112-31-9
SMILES
O=S(NC1=NOC=C1)(C2=CC(C=CC(N3C4=C(OC)C=C(C(F)=C4)C5=CC(Cl)=CC(F)=C5)=O)=C3C=C2)=O
分子式
C25H16ClF2N3O5S
分子量
543.93 g/mol
溶解性
Soluble in DMSO
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol