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首页-小分子抑制剂&激动剂-PI3K/Akt/mTOR Pathway-PI3K-PI3K-IN-16
PI3K-IN-16

Chemical Structure : PI3K-IN-16

CAS No.: 1895876-81-9

PI3K-IN-16 (PI3Kβ/δ inhibitor)

货号: PC-62708Not For Human Use, Lab Use Only.

PI3K-IN-16 is a potent and selective, orally bioavailable PI3Kβ and PI3Kδ inhibitor with cell IC50 of 12 nM (in PTEN null MDA-MB-468 cell) and 47 nM (in Jeko-1 B-cell), respectively.

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

    生物&药学活性

    PI3K-IN-16 is a potent and selective, orally bioavailable PI3Kβ and PI3Kδ inhibitor with cell IC50 of 12 nM (in PTEN null MDA-MB-468 cell) and 47 nM (in Jeko-1 B-cell), respectively.
    PI3K-IN-16  exhibits no significant activity on PI3Kα.
    PI3K-IN-16  shows profound pharmacodynamic modulation of AKT phosphorylation, excellent tumour growth inhibition in a mouse PTEN-deficient PC3 prostate tumour xenograft.

    物理化学性质&存储条件

    分子量 467.497
    分子式 C25H26FN3O5
    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

    8-((8-fluoro-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)methyl)-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

    参考文献

    1. Barlaam B, et al. Bioorg Med Chem Lett. 2016 May 1;26(9):2318-23.

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