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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-Sodium Channel-SSCI-1
SSCI-1

Chemical Structure : SSCI-1

CAS No.: 2101731-86-4

SSCI-1 (NaV1.7 inhibitor)

货号: PC-72208Not For Human Use, Lab Use Only.

SSCI-1 is a highly potent, selective NaV1.7 inhibitor with IC50 of 27 and 82 nM on human and rhesus Nav1.7 channels, respectively.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

    生物&药学活性

    SSCI-1 is a highly potent, selective NaV1.7 inhibitor with IC50 of 27 and 82 nM on human and rhesus Nav1.7 channels, respectively.
    SSCI-1 showed robust selectivity over other human and rhesus Nav channel paralogs, with the exception of Nav1.2 channels (IC50 252 nM for hNaV1.2), shows no other channels and receptors in 114 enzymatic, radioligand binding, and cellular assays.
    SSCI-1 also exhibits high potency in manual patch clamp experiments (IC50=66/295 nM for huma/rhesus Nav1.7 channels).
    SSCI-1 does not affect myelinated nerve excitability as measured by TT, SSCI-1 inhibits odorant-induced olfaction in the olfactory bulb of rhesus monkeys, measured by fMRI.
    SSCI-1 inhibits withdrawal responses to noxious heat in rhesus monkeys.

    物理化学性质&存储条件

    分子量 461.999
    分子式 C18H25ClFN5O2S2
    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

    (R)-5-chloro-2-fluoro-4-((4-((pyrrolidin-2-ylmethyl)amino)butyl)amino)-N-(thiazol-2-yl)benzenesulfonamide

    参考文献

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

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