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AZ 20
- Optical Purity: Optically pure
- Soluble in 0.1N HCl(aq) and DMSO
- MF: C21H24N4O3S
- MW: 412.51
Description
Potent, orally active and selective inhibitor of ATR protein kinase with monotherapy in vivo antitumor activity (IC50 value 5 nM). AZ 20 potently inhibits the growth of LoVo colorectal adenocarcinoma tumor cells in vitro, and is a useful compound to explore ATR pharmacology in vivo.
More Information
| Parent CAS No. | 1233339-22-4 |
|---|---|
| Chemical Name | (R)-4-(2-(1H-indol-4-yl)-6-(1-(methylsulfonyl)cyclopropyl)pyrimidin-4-yl)-3-methylmorpholine |
| SMILES | N1C2=C(C(C3=NC(C4(S(C)(=O)=O)CC4)=CC(N4CCOC[C@H]4C)=N3)=CC=C2)C=C1 |&1:21,r| |
| MFCD | N.A. |
| InChi | InChI=1S/C21H24N4O3S/c1-14-13-28-11-10-25(14)19-12-18(21(7-8-21)29(2,26)27)23-20(24-19)16-4-3-5-17-15(16)6-9-22-17/h3-6,9,12,14,22H,7-8,10-11,13H2,1-2H3/t14-/m1/s1 |
| InChiKey | SCGCBAAYLFTIJU-CQSZACIVSA-N |
| CID | 46244454 |
| Short Description | ATR inhibitor |
References
- K.M. Foote et al. Discovery of 4-{4-[(3R)-3-Methylmorpholin-4-yl]-6-[1-(methylsulfonyl)cyclopropyl]pyrimidin-2-yl}-1H-indole (AZ20): a potent and selective inhibitor of ATR protein kinase with monotherapy.... J. Med. Chem. 2013, 56, 2125-2138.
- M.R. Finlay et al. Modulation of DNA repair by pharmacological inhibitors of the PIKK protein kinase family. Bioorg. Med. Chem. Lett. 2012, 22, 5352-5359.
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