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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-SGLT-LX2761
LX2761

Chemical Structure : LX2761

CAS No.: 1610954-97-6

LX2761 (LX 2761, LX-2761)

货号: PC-60689Not For Human Use, Lab Use Only.

LX2761 is a potent, locally acting and orally bioavailable SGLT1 inhibitor that inhibits human SGLT1- and SGLT2-mediated glucose uptake with IC50 of 2.2 nM and 2.7 nM, respectively, restricted to the intestinal lumen.

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

    生物&药学活性

    LX2761 is a potent, locally acting and orally bioavailable SGLT1 inhibitor that inhibits human SGLT1- and SGLT2-mediated glucose uptake with IC50 of 2.2 nM and 2.7 nM, respectively, restricted to the intestinal lumen.
    LX2761 synergistically increases active GLP-1 levels combined with sitagliptin, lowers postprandial glucose, fasting glucose, and hemoglobin A1C, and increased plasma total GLP-1 in mice.
    LX2761 delays intestinal glucose absorption in vivo to improve glycemic control.

    物理化学性质&存储条件

    分子量 601.803
    分子式 C32H47N3O6S
    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

    N-(1-((2-(Dimethylamino)ethyl)amino)-2-methyl-1-oxopropan-2-yl)-4-(4-(2-methyl-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(methylthio)tetrahydro-2H-pyran-2-yl)benzyl)phenyl)-butanamide

    参考文献

    1. Goodwin NC, et al. J Med Chem. 2017 Jan 26;60(2):710-721.

    2. Powell DR, et al. J Pharmacol Exp Ther. 2017 Jul;362(1):85-97.

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