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首页-小分子抑制剂&激动剂-Cell Cycle/DNA Damage-Checkpoint Kinase (Chk)-MU 380
MU 380

Chemical Structure : MU 380

CAS No.: 2109805-78-7

MU 380 (MU-380;MU380)

货号: PC-60583Not For Human Use, Lab Use Only.

MU 380 is a novel potent, selective CHK1 inhibitor with IC50 of 2 nM, >80-fold selectivity over CHK2.

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

    生物&药学活性

    MU 380 is a novel potent, selective CHK1 inhibitor with IC50 of 2 nM, >80-fold selectivity over CHK2.
    MU 380  sensitizes a variety of tumor cell lines to hydroxyurea or gemcitabine up to 10 times.
    MU 380  shows extended inhibitory effects in cells, and unlike SCH900776, does not undergo in vivo N-dealkylation to the significantly less selective metabolite.
    MU 380  causes higher accumulation of DNA damage in tumor cells and subsequent enhanced cell death, and is more efficacious in the A2780 xenograft mouse model.

    物理化学性质&存储条件

    分子量 430.233
    分子式 C15H15BrF3N7
    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

    (R)-6-bromo-5-(piperidin-3-yl)-3-(1-(trifluoromethyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidin-7-amine

    参考文献

    1. Samadder P, et al. Mol Cancer Ther. 2017 Sep;16(9):1831-1842.

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