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VMY-1-103

Chemical Structure : VMY-1-103

CAS No.: 1209002-43-6

VMY-1-103 (VMY 1-103)

Catalog No.: PC-70177Not For Human Use, Lab Use Only.

VMY-1-103 is a dansylated analog of purvalanol B, and a CDK inhibitor that inhibits cell cycle progression and proliferation in prostate and breast cancer cells more effectively than purvalanol B.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

    Biological Activity

    VMY-1-103 is a dansylated analog of purvalanol B, and a CDK inhibitor that inhibits cell cycle progression and proliferation in prostate and breast cancer cells more effectively than purvalanol B.
    VMY-1-103 increases the sub G(1) fraction of apoptotic cells, induces PARP and caspase-3 cleavage and increases the levels of the death receptors DR4 and DR5, Bax and Bad.

    Physicochemical Properties

    M.Wt 708.27
    Formula C34H42ClN9O4S
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20 °C 12 Months; 4°C 6 Months
    In Solvent
    -80 °C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    2-Chloro-N-[2-[[[5-(dimethylamino)-1-naphthalenyl]sulfonyl]amino]ethyl]-4-[[2-[[(1R)-1-(hydroxymethyl)-2-methylpropyl]amino]-9-(1-methylethyl)-9H-purin-6-yl]amino]benzamide

    References

    1. Ringer L, et al. Cancer Biol Ther. 2011 Nov 1;12(9):818-26.

    2. Sirajuddin P, et al. Cell Cycle. 2012 Oct 15;11(20):3801-9.

    3. Waye S, et al. Aging (Albany NY). 2015 Oct;7(10):854-68.

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