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CDD-2693

Chemical Structure : CDD-2693

CAS No.:

CDD-2693 (CDD2693)

Catalog No.: PC-22284Not For Human Use, Lab Use Only.

CDD-2693 (CDD2693) is a potent, selective pan-ephrin receptor kinase (EPH receptor) inhibitor with binding Ki of 4.0/0.81 nM for EPHA2/EPHA4, respectively.

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    Biological Activity

    CDD-2693 (CDD2693) is a potent, selective pan-ephrin receptor kinase (EPH receptor) inhibitor with binding Ki of 4.0/0.81 nM for EPHA2/EPHA4, respectively.
    CDD-2693 shows nanomolar activity versus EPHA2 (IC50: 461 nM) and EPHA4 (IC50: 40 nM) but is a micromolar inhibitor of SRC, YES, and FGR.
    CDD-2693 significantly decreases EFNA5 (ligand) induced phosphorylation of EPHA2/4, decreases 12Z cell viability, and decreases IL-1β-mediated expression of prostaglandin synthase 2 (PTGS2) in 12Z endometriotic epithelial cells.
    CDD-2693 decreases expansion of primary endometrial epithelial organoids from patients with endometriosis and decreases Ewing's sarcoma viability.

    Physicochemical Properties

    M.Wt 489.59
    Formula C29H32FN3O3
    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

    1-(4-fluoro-2-(5'-hydroxy-2,2'-dimethyl-[1,1'-biphenyl]-4-carboxamido)-5-methylphenyl)-N-methylpiperidine-4-carboxamide

    References

    1. Madasu C, et al. Proc Natl Acad Sci U S A. 2024 May 7;121(19):e2322934121.

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