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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-iGluR-EU1622-240
EU1622-240

Chemical Structure : EU1622-240

CAS No.: 3057728-22-7

EU1622-240 (EU 1622-240)

货号: PC-23269Not For Human Use, Lab Use Only.

EU1622-240 is a positive allosteric modulator of NMDA receptors (NMDARs), preferentially potentiate GluN2B-, GluN2C-, and GluN2D-containing NMDARs with EC50 of 0.57 uM, 0.82 uM and 1.1 uM respectively.

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

    生物&药学活性

    EU1622-240 is a positive allosteric modulator of NMDA receptors (NMDARs), preferentially potentiate GluN2B-, GluN2C-, and GluN2D-containing NMDARs with EC50 of 0.57 uM, 0.82 uM and 1.1 uM respectively.
    EU1622-240 enhances current response to saturating agonist (doubling response amplitude at 0.2-0.5 µM).
    EU1622-240-bound NMDARs channels activated by a single agonist (glutamate or glycine) open to a unique conductance level with different pore properties and Mg2+ sensitivity, in contrast to channels arising from activation of NMDARs with both co-agonists bound.

    物理化学性质&存储条件

    分子量 478.31
    分子式 C20H14BrF2N3O2S
    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

    5-(3-bromo-4-fluorophenyl)-6-ethynyl-3-(2-(3-fluoro-3-methylazetidin-1-yl)-2-oxoethyl)thieno[2,3-d]pyrimidin-4(3H)-one

    参考文献

    1. Elijah Z Ullman, et al. Mol Pharmacol. 2024 Oct 23:MOLPHARM-AR-2024-001019.
    2. Fritzemeier RG, et al. J Med Chem. 2025 Apr 20. doi: 10.1021/acs.jmedchem.4c02912.

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