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AZD9362

Chemical Structure : AZD9362

CAS No.: 1905412-80-7

AZD9362 (AZD-9362, AZD 9362)

Catalog No.: PC-61142Not For Human Use, Lab Use Only.

AZD-9362 (AZD9362) is a potent, selective, orally bioavailable IGF-1R inhibitor with IC50 of 14 nM.

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

    Biological Activity

    AZD-9362 (AZD9362) is a potent, selective, orally bioavailable IGF-1R inhibitor with IC50 of 14 nM.
    AZD-9362 weakly inhibits CDK1/2/7/8/9 with IC50 of 300-800 nM, displays good kinase selectivity in a panel of 60 kinases.
    AZD-9362 inhibits the auto-phosphorylation of IGF-1R after IGF1 stimulation in mice fibroblasts with IC50 of 48 nM, inhibits IGF-driven growth of tumour allografts.

    Physicochemical Properties

    M.Wt 494.984
    Formula C24H27ClN8O2
    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

    (2R)-1-[4-(4-{[5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)-2-pyrimidinyl]amino}-3,5-dimethyl-1H-pyrazol-1-yl)-1-piperidinyl]-2-hydroxy-1-propanone

    References

    1. Degorce SL, et al. J Med Chem. 2016 May 26;59(10):4859-66.

    2. Fox EM, et al. Breast Cancer Res. 2013;15(4):R55.

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