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Saracatinib

Chemical Structure : Saracatinib

CAS No.: 379231-04-6

Saracatinib (AZD0530;AZD-0530;AZD 0530)

Catalog No.: PC-42475Not For Human Use, Lab Use Only.

Saracatinib (AZD0530) is a potent, highly selective, orally available, dual Src/Abl kinase inhibitor with IC50 of 2.7, 4, 4 and 30 nM for c-Src, Yes, Lck and Abl, respectively.

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

Biological Activity

Saracatinib (AZD0530) is a potent, highly selective, orally available, dual Src/Abl kinase inhibitor with IC50 of 2.7, 4, 4 and 30 nM for c-Src, Yes, Lck and Abl, respectively.
Saracatinib (AZD0530) displays high selectivity over a range of kinases (Csk, VEGFR-2, Flt-4, EGFR, and PDGFR).
Saracatinib (AZD0530) exhibits potent inhibition of tumor growth in a c-Src-transfected 3T3-fibroblast xenograft model in vivo.

Physicochemical Properties

M.Wt 542.0265
Formula C27H32ClN5O5
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

DMSO: ≥ 32 mg/mL

Chemical Name/SMILES

4-Quinazolinamine, N-(5-chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methyl-1-piperazinyl)ethoxy]-5-[(tetrahydro-2H-pyran-4-yl)oxy]-

References

1. Hennequin LF, et al. J Med Chem. 2006 Nov 2;49(22):6465-88.

2. Herynk MH, et al. Mol Cancer Ther. 2006 Dec;5(12):3023-31.

3. Chang YM, et al. Oncogene. 2008 Oct 23;27(49):6365-75.

4. Gwanmesia PM, et al. BMC Cancer. 2009 Feb 13;9:53.

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