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首页-小分子抑制剂&激动剂-Cell Cycle/DNA Damage-PARP-AZ0108
AZ0108

Chemical Structure : AZ0108

CAS No.: 1825345-52-5

AZ0108 (AZ-0108)

货号: PC-62698Not For Human Use, Lab Use Only.

AZ0108 is an orally bioavailable phthalazinone PARP inhibitor with enzyme IC50 of <30/<30/83 nM for PARP1/2/6 respectively.

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

    生物&药学活性

    AZ0108 is an orally bioavailable phthalazinone PARP inhibitor with enzyme IC50 of <30/<30/83 nM for PARP1/2/6 respectively.
    AZ0108 displays >100-fold selectivity against PARP3/TNKS1/TNKS2 (IC50=2.8/3.2/>3 uM).
    AZ0108 blocks centrosome clustering in HeLa cell with IC50 of 83 nM.
    AZ0108 has been utilized as in vitro tool and in vivo probe to investigate the bio- logical consequences of inhibiting centrosome clustering through PARP enzymes.

    物理化学性质&存储条件

    分子量 500.458
    分子式 1825345-52-5
    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

    (S)-4-((3-(3-(1,1-difluoroethyl)-6-methyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine-7-carbonyl)phenyl)difluoromethyl)phthalazin-1(2H)-one

    参考文献

    1. Johannes JW, et al. Bioorg Med Chem Lett. 2015 Dec 15;25(24):5743-7.

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