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AZD-9362

Chemical Structure : AZD-9362

CAS No.: 1905412-80-7

AZD-9362 (AZD 9362;AZD9362)

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)

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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