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首页-小分子抑制剂&激动剂-GPCR-GPR119-JTP-109192
JTP-109192

Chemical Structure : JTP-109192

CAS No.: 2211076-86-5

JTP-109192 (JTP109192)

货号: PC-20442Not For Human Use, Lab Use Only.

JTP-109192 (JTP109192) is a potent GPR119 agonist with EC50 of 3.6. 4.5 and 5.2 nM for human, rat and mouse GPR119 respectively (increased intracellular cAMP levels).

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

    生物&药学活性

    JTP-109192 (JTP109192) is a potent GPR119 agonist with EC50 of 3.6. 4.5 and 5.2 nM for human, rat and mouse GPR119 respectively (increased intracellular cAMP levels).
    JTP-109192 (0.1-10 uM) significantly increased GLP-1 secretion in GLUTag cells, at 10 uM, 5.6 -fold increase by JTP-109192 was observed as compared with DMSO alone.
    JTP-109192 enhanced glucose stimulated insulin secretion (GSIS) in the INS1E cells.
    A single administration of JTP-109192 (10 mg/kg) enhanced GSIS at high blood glucose levels in Sprague-Dawley (SD) rats.
    A repeated administrations (10 mg/kg) in ZF rats improved glucose metabolism without lack of drug efficacy (tachyphylaxis) and increased glucose infusion rates due to improvement of insulin sensitivity.

    物理化学性质&存储条件

    分子量 401.59
    分子式 C25H39NO3
    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

    4-((5-((5r,8s)-3,3-dimethyl-2-oxaspiro[4.5]decan-8-yl)pentyl)oxy)-N,N-dimethylbenzamide

    参考文献

    1. Hironobu Tadaki, et al. Clin Exp Pharmacol Physiol. 2019 Oct;46(10):910-919.

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