Total item
Cart Subtotal
$0.00 Biological Activity
AZD7762 is a potent ATP-competitive checkpoint kinase inhibitor that drives checkpoint abrogation and potentiates DNA-targeted therapies.
Targets
| Chk1 (Cell-free assay) | Chk2 (Cell-free assay) | |||
| 5 nM | <10 nM |
| In vitro | DMSO | 50 mg/mL (137.96 mM) | |
| Water | <1 mg/mL (<1 mM) | ||
| Ethanol | <1 mg/mL (<1 mM) | ||
|
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
|||
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.1 mM | 27.59 mL | 137.97 mL | 275.94 mL |
| 0.5 mM | 5.52 mL | 27.59 mL | 55.19 mL |
| 1 mM | 2.76 mL | 13.8 mL | 27.59 mL |
| 5 mM | 0.55 mL | 2.76 mL | 5.52 mL |
*The above data is based on the productmolecular weight 362.4 . Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Catalog Num | A10113 |
|---|---|
| Actions | Inhibitor |
| M. Wt | 362.4 |
| Formula | C17H19FN4O2S |
| Solubility | DMSO |
| Purity | >98% |
| Storage | at -20°C 3 years Powder |
| CAS No. | 860352-01-8 |
| Synonyms | AZD-7762 |
| SMILES | C1C[[email protected]@H](CNC1)NC(=O)C2=C(C=C(S2)C3=CC(=CC=C3)F)NC(=O)N |
Product Tags
Product Questions
Product Questions
No Questions
You may also be interested in the following product(s)
LY2603618 (IC-83)
LY2603618 is a chk2 inhibitor that binds to and inhibits the activity of chk2, which may prevent the repair of DNA caused by DNA-damaging ag…
CCT241533 hydrochloride
CCT241533 Hcl is a potent serine/threonine checkpoint kinase (Chk2) inhibitor with IC50 of 3 nM; shows minimal cross-reactivity against a pa…
PF 477736
PF 477736 is a selective checkpoint kinase 1 (Chk1) inhibitor (Ki values are 0.49 and 47 nM for Chk1 and Chk2 respectively).
CCT241533
CCT241533 is a potent and selective Inhibitor of CHK2 that potentiates the cytotoxicity of PARP inhibitors.
MK-1775
MK-1775 is a potent and selective Wee1 kinase inhibitor in vitro and in vivo.
CCT244747
CCT244747 is a novel potent, highly selective, orally active ATP-competitive CHK1 inhibitor with potential anticancer activity,
BML-277
BML-277 (Chk2 Inhibitor II) is a Chk2 (checkpoint kinase 2) inhibitor.
SCH 900776 (MK-8776)
SCH900776 is an agent targeting cell cycle checkpoint kinase 1 (Chk1) with potential radiosensitization and chemosensitization activities. I…
Keywords:buy AZD7762 | AZD7762 Supplier | purchase | cost | manufacturer | order | distributor | buy 860352-01-8| 860352-01-8 Supplier | purchase 860352-01-8 | 860352-01-8 cost | 860352-01-8 manufacturer | order 860352-01-8 | 860352-01-8 distributor
Adooq Quality Guarantee
We promise all products perform as described.