AZD 7762 hydrochloride
Tocris Bioscience, part of Bio-Techne | Catalog # 5199
Potent and selective ATP-competitive inhibitor of Chk1 and Chk2; also enhances CRISPR-Cpf1-mediated genome editing
Discontinued Product
5199 has been discontinued.
View all Checkpoint Kinase Inhibitors products.
Key Product Details
Description
Potent and selective ATP-competitive inhibitor of Chk1 and Chk2; also enhances CRISPR-Cpf1-mediated genome editing
Product Description
AZD 7762 hydrochloride is a potent and selective ATP-competitive inhibitor of Chk1 and Chk2 (IC50 vales are 5 nM for both kinases); displays at least >10 fold selectivity over a panel of 164 kinases. Potentiates cytotoxicity of DNA-damaging agents. Active in vivo. Also improves efficiency of CRISPR-Cpf1-mediated genome editing in hPSC lines (2.7-fold at 1 μM).Licensing Information
Sold for research purposes under agreement from AstraZenecaProduct Specifications
Molecular Weight
398.88
Formula
C17H19FN4O2S.HCl
Storage
Store at -20°C
Purity
≥98% (HPLC)
Chemical Name
3-[(Aminocarbonyl)amino]-5-(3-fluorophenyl)-N-(3S)-3-piperidinyl-2-thiophenecarboxamide hydrochloride
CAS Number
1246094-78-9
PubChem ID
56972142
InChI Key
WFZBLOIXZRZEDG-YDALLXLXSA-N
SMILES
FC1=CC=CC(C2=CC(NC(N)=O)=C(C(N[C@@H]3CNCCC3)=O)S2)=C1.Cl
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| water | 39.89 | 100 | |
| DMSO | 39.89 | 100 |
Preparing Stock Solutions
for AZD 7762 hydrochloride
The following data is based on the product molecular weight 398.88
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.51 mL | 12.54 mL | 25.07 mL |
| 5 mM | 0.50 mL | 2.51 mL | 5.01 mL |
| 10 mM | 0.25 mL | 1.25 mL | 2.51 mL |
| 50 mM | 0.05 mL | 0.25 mL | 0.50 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Morgan Mechanism of radiosensitization by the Chk1/2 inhibitor AZD7762 involves abrogation of the G2 checkpoint and inhibition of homologous recombinational DNA repair. Cancer Res. 2010 PMID: 20501833
- Ma Small molecules promote CRISPR-Cpf1-mediated genome editing in human pluripotent stem cells. Nat Commun. 2018 PMID: 29610531
- Zabludoff AZD7762, a novel checkpoint kinase inhibitor, drives checkpoint abrogation and potentiates DNA-targeted therapies. Mol. Cancer Ther. 2008 PMID: 18790776
Product Specific Notices for AZD 7762 hydrochloride
For research use only
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