( E )‐3‐X‐indoline‐2‐ones as potent and selective inhibitors against different receptor tyrosine kinase (RTKs) in solution vs gas phase, at DFT
Author:
Affiliation:
1. Department of Chemistry, Karaj BranchIslamic Azad University Karaj Iran
2. Young Researchers and Elites Club, North Tehran BranchIslamic Azad University Tehran Iran
Funder
Islamic Azad University
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/poc.3929
Reference49 articles.
1. The Thionium/N-Acyliminium Ion Cyclization Cascade as a Strategy for the Synthesis of Azapolycyclic Ring Systems
2. Synthesis and anti-tyrosine kinase activity of 3-(substituted-benzylidene)-1, 3-dihydro-indolin derivatives: investigation of their role against p60c-Src receptor tyrosine kinase with the application of receptor docking studies
3. Comparison of some 3-(substituted-benzylidene)-1, 3-dihydro-indolin derivatives as ligands of tyrosine kinase based on binding mode studies and biological assay
4. Recent Advances in the Synthesis of Indole and Quinoline Derivatives through Cascade Reactions
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