SSCI-2 | Nav1.7 inhibitor | Probechem Biochemicals

Chemical Structure : SSCI-2

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SSCI-2 (NaV1.7 inhibitor)

货号: PC-72209Not For Human Use, Lab Use Only.

SSCI-2 is a highly potent, selective NaV1.7 inhibitor with IC50 of 9 and 17 nM on human and rhesus Nav1.7 channels, respectively.

规格	价格	库存	数量
25 mg		Get quote
50 mg		Get quote
100 mg		Get quote

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生物&药学活性

SSCI-2 is a highly potent, selective NaV1.7 inhibitor with IC50 of 9 and 17 nM on human and rhesus Nav1.7 channels, respectively.
SSCI-2 showed robust selectivity over other human and rhesus Nav channel paralogs, with the exception of Nav1.2 channels (IC50 183 nM for hNaV1.2), shows no other channels and receptors in 114 enzymatic, radioligand binding, and cellular assays.
SSCI-2 also exhibits high potency in manual patch clamp experiments (IC50=24/62 nM for huma/rhesus Nav1.7 channels).
SSCI-2 inhibits withdrawal responses to noxious heat in rhesus monkeys.

物理化学性质&存储条件

分子量	474.59
分子式	C19H28F2N6O2S2
外观性状	Solid
CAS No.
储存条件	固体粉末 -20°C 12 个月; 4°C 6 个月	配置液 -80°C 6 个月; -20°C 6 个月
Shipping
Solubility	10 mM in DMSO
Chemical Name/SMILES	4-(((2S,3R)-3-amino-2-((1-(2-aminoethyl)cyclobutyl)methyl)butyl)amino)-2,5-difluoro-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide

参考文献

1. Kraus RL, et al. Sci Transl Med. 2021 May 19;13(594):eaay1050.