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CXL017

Chemical Structure : CXL017

CAS No.: 1063714-11-3

CXL017 (CXL-017)

Catalog No.: PC-62866Not For Human Use, Lab Use Only.

CXL017 is a small molecule that has selective cytotoxicity toward MDR cancer cell lines in vitro, through inhibition of the sarco/endoplasmic reticulum Ca(2+)-ATPase (SERCA) with IC50 of 15 uM.

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

    Biological Activity

    CXL017 is a small molecule that has selective cytotoxicity toward MDR cancer cell lines in vitro, through inhibition of the sarco/endoplasmic reticulum Ca(2+)-ATPase (SERCA) with IC50 of 15 uM.
    CXL017 selectively suppresses the growth of tumors derived from the MDR cancer cell line, HL60/MX2, in vivo.
    CXL017 significantly downregulates Mcl-1 and Bax and up-regulates Noxa, Bim, Bcl-XL, SERCA2, and SERCA3 proteins, along with a reduction in endoplasmic reticulum (ER) calcium content in HL60/MX2 cells.
    CXL017 elicits its cytotoxic effect, in part, through inhibition of the SERCA.

    Physicochemical Properties

    M.Wt 441.48
    Formula C24H27NO7
    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

    Ethyl 2-amino-6-(3,5-dimethoxyphenyl)-4-(2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate

    References

    1. Das SG, et al. ACS Chem Biol. 2013 Feb 15;8(2):327-35.

    2. Aridoss G, et al. J Med Chem. 2012 Jun 14;55(11):5566-81.

    3. Hermanson DL, et al. Mol Pharmacol. 2013 Aug;84(2):236-43.

    4. Bleeker NP, et al. Mol Pharm. 2013 Nov 4;10(11):4358-66.

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