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首页-小分子抑制剂&激动剂-Metabolic Enzyme/Protease-Phosphodiesterase (PDE)-TC-E 5005
TC-E 5005

Chemical Structure : TC-E 5005

CAS No.: 959705-64-7

TC-E 5005 (TCE-5005, TC-E-5005)

货号: PC-61347Not For Human Use, Lab Use Only.

TC-E 5005 is a potent and selective PDE10A inhibitor with IC50 of 7.28 nM.

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

    生物&药学活性

    TC-E 5005 is a potent and selective PDE10A inhibitor with IC50 of 7.28 nM.
    TC-E 5005 displays 30-500-fold selectivity over PDE10A, 2A, 11A, 5A, 7B and 3A, shows no inhibitory activity for PDE1B, 4A, 6, 8A and 9A (IC50>5 uM).
    TC-E 5005 reverses stereotypy and hyperactivity induced by MK-801 in rats.
    TC-E 5005 also inhibits adrenergic and neurogenic smooth muscle contractions in the human prostate, inhibits neurogenic contractions with similar efficacy than tadalafil.

    物理化学性质&存储条件

    分子量 270.33
    分子式 C15H18N4O
    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

    2-Methoxy-6,7-dimethyl-9-propylimidazo[1,5-a]pyrido[3,2-e]pyrazine

    参考文献

    1. Höfgen N, et al. J Med Chem. 2010 Jun 10;53(11):4399-411.

    2. Hennenberg M, et al. Prostate. 2016 Nov;76(15):1364-74.

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