[CAS NO. 905973-89-9]  CGK 733

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PRODUCTS SPECIFICATIONS [905973-89-9]

Store
Catalog
SLK-S7136
Brand
Selleck
CAS
905973-89-9

DESCRIPTION [905973-89-9]

Overview

MDLMFCD09038682
Molecular Weight555.84
Molecular FormulaC23H18Cl3FN4O3S
SMILESO=C(NC(NC(NC1=CC=C(F)C([N+]([O-])=O)=C1)=S)C(Cl)(Cl)Cl)C(C2=CC=CC=C2)C3=CC=CC=C3

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 mM1.7991 mL8.9954 mL17.9908 mL
5 mM0.3598 mL1.7991 mL3.5982 mL
10 mM0.1799 mL0.8995 mL1.7991 mL
50 mM0.0360 mL0.1799 mL0.3598 mL

Description

CGK 733 is a potent and selective inhibitor of with of ~200 nM.

Targets

ATM [1]ATR [1]
200 nM 200 nM

In vitro

CGK733 is able to confer robust growth to senescent cells that have ceased proliferation. Senescence-associated β-galactosidase (SA–β-gal) activity disappears in CGK733-treated cells. CGK733 shows greater potency in inhibiting ATM/ATR than LY294002 (IC50 , ~5 μM for ATM and ATR), a pan-inhibitor of PI3K and PIKKs. CGK733 (30 μM) treated for 24h causes ~60% cell death in senescent MCF-7 cells. CGK733 (20 μM) induces the loss of cyclin D1 via the ubiquitin- dependent proteasomal degradation pathway in MCF-7 and T47D breast cancer cell lines. CGK733 at concentrations ranging from 0.6- 40 μM, inhibits proliferation of MCF-7 and T47D estrogen receptor (ER) positive breast cancer cells, MDA-MB436 ER negative breast cancer cells, LnCap pros-tate cancer cells and HCT116 colon cancer cells. Furthermore, CGK733 also suppresses proliferation of non- transformed mouse BALB/c 3T3 embryonic fibroblast cells. The CGK733-mediated inhibition of proliferation is dose dependent and significant at doses as low as 2.5 μM.