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AZD7762 hydrochloride

Axon 1399
Based on 275 publications in PubMed
  • Parent CAS:  860352-01-8
  • Optical Purity:  >98% e.e.
  • Soluble in water and DMSO
  • MF:  C17H19FN4O2S.HCl
  • MW:  398.88

Description

AZD7762 hydrochloride is a potent checkpoint kinase 1 and 2 inhibitor with reported IC50 values of approximately 5 nM for both CHK1 and CHK2.

AZD7762 suppresses DNA-damage checkpoint signaling, promotes premature cell-cycle progression and enhances the cytotoxicity of genotoxic agents. It is used to investigate checkpoint dependency, replication stress and radiosensitization.

Key Features

  • Potent dual CHK1/CHK2 inhibitor
  • Reported IC50: approximately 5 nM
  • Abrogates S- and G2-phase DNA-damage checkpoints
  • Sensitizes cells to chemotherapy and radiation

Applications

  • CHK1 and CHK2 kinase assays
  • DNA-damage checkpoint research
  • Replication-stress and cell-cycle studies
  • Chemo- and radiosensitization models

More Information

Certificate of Analysis

Material Safety Data Sheet

Parent CAS No. 860352-01-8
Chemical Name 5-(3-Fluoro-phenyl)-3-ureido-thiophene-2-carboxylic acid (S)-piperidin-3-ylamide hydrochloride
SMILES C1(NC(N)=O)=C(C(N[C@H]2CCCNC2)=O)SC(C2C=CC=C(F)C=2)=C1.Cl |&1:8,r|
MFCD N.A.
InChi InChI=1S/C17H19FN4O2S.ClH/c18-11-4-1-3-10(7-11)14-8-13(22-17(19)24)15(25-14)16(23)21-12-5-2-6-20-9-12;/h1,3-4,7-8,12,20H,2,5-6,9H2,(H,21,23)(H3,19,22,24);1H/t12-;/m0./s1
InChiKey WFZBLOIXZRZEDG-YDALLXLXSA-N
CID 56972142
Short Description CHK inhibitor

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