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首页-小分子抑制剂&激动剂-GPCR-Neurotensin Receptor-SR142948
SR142948

Chemical Structure : SR142948

CAS No.: 184162-64-9

SR142948 (SR 142948)

货号: PC-60948Not For Human Use, Lab Use Only.

SR142948 is a potent, selective and orally active neurotensin receptor antagonist with IC50 of 1.19 nM.

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

    生物&药学活性

    SR142948 is a potent, selective and orally active neurotensin receptor antagonist with IC50 of 1.19 nM.
    SR142948 antagonizes neurotensin-induced inositol monophosphate formation in HT 29 cells with IC50 of 3.9 nM.
    SR142948 inhibits the turning behavior induced by neurotensin in mice, completely antagonizes neurotensin-evoked acetylcholine release in the rat striatum at 0.1 mg/kg.
    SR142948 also blocks both hypothermia and analgesia induced by i.c.v. injection of neurotensin injection into the ventral tegmental area.

    物理化学性质&存储条件

    分子量 685.87
    分子式 C39H51N5O6
    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-[[5-(2,6-dimethoxyphenyl)-1-[4-(3-dimethylaminopropyl-methylcarbamoyl)-2-propan-2-ylphenyl]pyrazole-3-carbonyl]amino]adamantane-2-carboxylic acid

    参考文献

    1. Gully D, et al. J Pharmacol Exp Ther. 1997 Feb;280(2):802-12.

    2. Betancur C, et al. Eur J Pharmacol. 1998 Feb 5;343(1):67-77.

    3. Schaeffer P, et al. J Cardiovasc Pharmacol. 1998 Apr;31(4):545-50.

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