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AZD6738

Known as: ATR Kinase Inhibitor AZD6738, AZD-6738 
An orally available morpholino-pyrimidine-based inhibitor of ataxia telangiectasia and rad3 related (ATR) kinase, with potential antineoplastic… 
National Institutes of Health

Papers overview

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Highly Cited
2020
Highly Cited
2020
Background Radioimmunotherapy has a promising antitumor effect in hepatocellular carcinoma (HCC), depending on the regulatory… 
Highly Cited
2019
Highly Cited
2019
Purpose: ATR inhibitors (ATRi) are in early phase clinical trials and have been shown to sensitize to chemotherapy and… 
Highly Cited
2018
Highly Cited
2018
DNA-damaging chemotherapy and radiation therapy are integrated into the treatment paradigm of the majority of cancer patients… 
Highly Cited
2018
Highly Cited
2018
The kinase ataxia telangiectasia mutated and rad3 related (ATR) is a key regulator of the DNA-damage response and the apical… 
Highly Cited
2018
Highly Cited
2018
Pancreatic ductal adenocarcinoma (PDAC) is among the deadliest cancers, and overall survival rates have barely improved over the… 
2017
2017
Ataxia telangiectasia and Rad3‐related (ATR) proteins are sensors of DNA damage, which induces homologous recombination (HR… 
Highly Cited
2016
Highly Cited
2016
AZD6738 is an orally active ATR inhibitor (ATRi) currently in phase I clinical trials. We found in vitro growth inhibitory… 
2015
2015
Understanding the therapeutic effect of drug dose and scheduling is critical to inform the design and implementation of clinical… 
Review
2015
Review
2015
The human ATR gene encodes a kinase that is activated by DNA damage and replication stress as a central transducer of a…