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

Chemical Structure : Debromohymenialdisine

CAS No.: 75593-17-8

Debromohymenialdisine (SKF-108753;SKF108753)

货号: PC-60291Not For Human Use, Lab Use Only.

Debromohymenialdisine (SKF108753) is a marine sponge alkaloid that inhibits Chk1 and Chk2 with IC50 of 3 and 3.5 uM, respectively.

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

    生物&药学活性

    Debromohymenialdisine (SKF108753) is a marine sponge alkaloid that inhibits Chk1 and Chk2 with IC50 of 3 and 3.5 uM, respectively.
    Debromohymenialdisine also inhibits MAP kinase kinase 1 (IC50=881 nM), GSK3β (IC50=1.39 uM), and CDK5/p25 (IC50=9.12 uM), does not significantly affect ATM and ATR.
    Debromohymenialdisine blocks G2 arrest in cancer cells.

    物理化学性质&存储条件

    分子量 245.2
    分子式 C11H11N5O2
    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

    (4Z)-4-(2-amino-1,5-dihydro-5-oxo-4H-imidazol-4-ylidene)-4,5,6,7-tetrahydro-pyrrolo[2,3-c]azepin-8(1H)-one

    参考文献

    1. Curman D, et al. J Biol Chem. 2001 May 25;276(21):17914-9.

    2. Saleem RS, et al. Bioorg Med Chem. 2012 Feb 15;20(4):1475-81.

    3. Jobson AG, et al. Mol Pharmacol. 2007 Oct;72(4):876-84.

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