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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-Potassium Channel-SCR2682
SCR2682

Chemical Structure : SCR2682

CAS No.: 1584711-40-9

SCR2682 (SCR 2682)

货号: PC-49538Not For Human Use, Lab Use Only.

SCR2682 is a potent, selective neuronal voltage-gated potassium Kv7/KCNQ/M channel opener (activator) with EC50 of 9.8 nM (Kv7.2/Kv7.3), 100-fold more potency than retigabine.

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

    生物&药学活性

    SCR2682 is a potent, selective neuronal voltage-gated potassium Kv7/KCNQ/M channel opener (activator) with EC50 of 9.8 nM (Kv7.2/Kv7.3), 100-fold more potency than retigabine.
    SCR2682 shifts voltage-dependent activation of the Kv7.2/7.3 current toward more negative membrane potential, to about −37 mV (V1/2).
    SCR2682 also activates the native M-current in rat hippocampal or cortical neurons, causing marked hyperpolarization and potent inhibition of neuronal firings.
    Intraperitoneal or intragastric administration of SCR2682 results in a dose-dependent inhibition of seizures by maximal electroshock.
    SCR2682 also decreases epileptiform discharges in KA-induced seizures

    物理化学性质&存储条件

    分子量 435.424
    分子式 C21H27BrN2OS
    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

    N-(4-(2-bromo-6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)-2,6-dimethylphenyl)-3,3-dimethylbutanamide

    参考文献

    1. Wang J, et al. J Pharmacol Exp Ther. 2021 Apr;377(1):20-28.

    2. Zhuang XF, et al. J Pharmacol Exp Ther. 2022 Nov 17:JPET-AR-2022-001328.

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