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首页-小分子抑制剂&激动剂-GPCR-Sigma Receptor-DKR-1677
DKR-1677

Chemical Structure : DKR-1677

CAS No.: 2095102-44-4

DKR-1677 (DKR1677)

货号: PC-20740Not For Human Use, Lab Use Only.

DKR-1677 (DKR1677) is a potent, selective σ2R/TMEM97 modulator with Ki value of 5.1 nM, 45-fold selectivity over σ1R (Ki=230 nM).

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

    生物&药学活性

    DKR-1677 (DKR1677) is a potent, selective σ2R/TMEM97 modulator with Ki value of 5.1 nM, 45-fold selectivity over σ1R (Ki=230 nM).
    DKR-1677 generally exhibits greater than 100-fold selectivity against a panel of more than 50 proteins relevant to the central nervous system (CNS), with the exception of histamine-1 (20-fold) and the alpha-2A adrenergic (68-fold) receptors.
    DKR-1677 is neuroprotective after blast-induced and controlled cortical impact (CCI) TBI in mice.
    DKR-1677 decreases axonal degeneration after blast-induced TBI and enhances survival of cortical neurons and oligodendrocytes after CCI injury.
    DKR-1677 preserves cognition in the Morris water maze after blast TBI.

    物理化学性质&存储条件

    分子量 419.57
    分子式 C26H33N3O2
    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

    benzyl 8-(4-propylpiperazin-1-yl)-1,3,4,5-tetrahydro-2H-1,5-methanobenzo[c]azepine-2-carboxylate

    参考文献

    1. Vázquez-Rosa E, et al. ACS Chem Neurosci. 2019 Mar 20;10(3):1595-1602.

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