Styrylquinazoline derivatives as ABL inhibitors selective for different DFG orientations-Reference-Cited by-同舟云学术

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Styrylquinazoline derivatives as ABL inhibitors selective for different DFG orientations

Published:2023-04-18 Issue:1 Volume:38 Page:
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Malarz Katarzyna¹,Mularski Jacek²,Pacholczyk Marcin³,Musiol Robert²

Affiliation:

1. Institute of Physics, University of Silesia in Katowice, Chorzów, Poland

2. Institute of Chemistry, University of Silesia in Katowice, Chorzów, Poland

3. Department of Systems Biology and Engineering, Silesian University of Technology, Gliwice, Poland

Funder

National Science Centre

Silesian University of Technology

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/14756366.2023.2201410

Reference67 articles.

1. Activation of tyrosine kinases by mutation of the gatekeeper threonine

2. NMR reveals the allosteric opening and closing of Abelson tyrosine kinase by ATP-site and myristoyl pocket inhibitors

3. Abl N-Terminal Cap Stabilization of SH3 Domain Dynamics

4. Structure and Dynamic Regulation of Abl Kinases*

5. Discovery of Allosteric Bcr–Abl Inhibitors from Phenotypic Screen to Clinical Candidate

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