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AZD-7762 Chemical Structure

AZD-7762

Data Sheet For research use only. Not for human use.
Cat. No. :BCP01893CAS No. :860352-01-8Purity:98%
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  • Chemical Properties&Biological Activity
CAS No. 860352-01-8 Cat. No. BCP01893
Name AZD-7762
Synonyms AZD7762;AZD 7762;
SMILES
Chemical Name
Formula C17H19FN4O2S M. Wt 362.42
Purity 98% Storage Store at 4-8°C
Description AZD7762, a more selective Chk1 inhibitor, inhibits Chk1 phosphorylation of a cdc25C peptide by reversibly binding to the ATP-binding site of Chk1, with IC50 of 5 nM and Ki of 3.6 nM. AZD7762 induces cell arrest with EC50 of 0.620 μM, and significantly abrogates the camptothecin induced G2 arrest with an EC50 of 10 nM, by blocking the chk1 dependent degradation of Cdc25A and activation of Cyclin A. AZD7762 (300 nM) enhances the antitumor efficacy of gemcitabine against SW620 and topotecan against MDA-MB-231 by reducing the GI50 values from 24.1 nM and 2.25 μM to 1.08 nM and 0.15 μM, respectively. AZD7762 shows cytotoxicity against a variety of neuroblastoma cell lines bearing p53 wild type, p53 mutation, Mdm2 amplification or p14 deletion with IC50 values ranging from 82.6-505.9 nM.
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