[CAS NO. 1080622-86-1]  CP-466722

Ships within Stock Price Qty Total
$0.00
$0.00
Please click "REQUEST A QUOTE" button if you need other sizes or custom synthesis
request a quote
If there is no stock, or you need other sizes or custom synthesis, please:

PRODUCTS SPECIFICATIONS [1080622-86-1]

Store
Catalog
SLK-S2245
Brand
Selleck
CAS
1080622-86-1

DESCRIPTION [1080622-86-1]

Overview

MDLMFCD17392566
Molecular Weight349.35
Molecular FormulaC17H15N7O2
SMILESNC1=NC(C2=NC=CC=C2)=NN1C3=C4C=C(OC)C(OC)=CC4=NC=N3

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM2.8625 mL14.3123 mL28.6246 mL
5 mM0.5725 mL2.8625 mL5.7249 mL
10 mM0.2862 mL1.4312 mL2.8625 mL
50 mM---

Description

CP-466722 is a potent and reversible inhibitor, does not affect ATR and inhibits PI3K or PIKK family members in cells.

Targets

ATM [2]
410 nM

In vitro

In vitro, CP-466722 is identified as a potential inhibitor to decrease the activity of purified ATM kinase to phosphorylate GST-p53(1–101) substrate. In addition, CP-466722 also shows the inhibitory activities against abl and src kinases. In HeLa cells, CP-466722 at doses of 6μM, results in the inhibition in ATM-dependent phosphorylation by reversibly inhibiting ionizing radiation (IR)-induced ATM kinase activity. Besides, ATM-dependent p53 induction is also inhibited by CP-466722 in MCF-7 human breast cancer cells and primary and immortalized diploid human fibroblasts. In response to IR, CP-466722 increased proportion of cells with G2/M DNA content and reduces proportion of cells with G1-phase DNA content in HeLa cells. Transient exposure to CP-466722 for a period of 4 hours sensitizes HeLa cells to IR without affecting cell plating nor cell viability.