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VE 822

 - Berzosertib  - VX 970
Axon 2452
CAS:  1232416-25-9
Purity:  99%
  • Soluble in 0.1N HCl(aq) and DMSO
  • MF:  C24H25N5O3S
  • MW:  463.55

Description

VE 822 (Berzosertib) is a selective inhibitor of ATR kinase, a core regulator of replication-stress and DNA-damage checkpoint signaling. It sensitizes cancer cells to DNA damage by weakening checkpoint maintenance and homologous recombination responses.

ATR coordinates cell-cycle arrest, replication fork stability and repair signaling after DNA damage or replication stress. VE 822 is a valuable tool for studying DNA-damage response pharmacology and combination strategies with radiation or genotoxic agents.

Key Features

  • Selective ATR kinase inhibitor
  • Reported IC50 values: 0.019 µM for ATR, 2.6 µM for ATM and 18.1 µM for DNA-PK
  • Disrupts checkpoint maintenance and homologous recombination after irradiation
  • Enhances sensitivity to DNA-damaging treatments in cancer models

Applications

  • DNA-damage response research
  • ATR checkpoint signaling assays
  • Radiosensitization and combination-treatment studies
  • Cancer cell replication-stress models

More Information

Certificate of Analysis

Material Safety Data Sheet

Parent CAS No. 1232416-25-9
Chemical Name 5-(4-(isopropylsulfonyl)phenyl)-3-(3-(4-((methylamino)methyl)phenyl)isoxazol-5-yl)pyrazin-2-amine
SMILES C1(N)=NC=C(C2=CC=C(S(C(C)C)(=O)=O)C=C2)N=C1C1ON=C(C2=CC=C(CNC)C=C2)C=1
MFCD N.A.
InChi InChI=1S/C24H25N5O3S/c1-15(2)33(30,31)19-10-8-18(9-11-19)21-14-27-24(25)23(28-21)22-12-20(29-32-22)17-6-4-16(5-7-17)13-26-3/h4-12,14-15,26H,13H2,1-3H3,(H2,25,27)
InChiKey JZCWLJDSIRUGIN-UHFFFAOYSA-N
CID 59472121
Short Description ATR inhibitor

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