Novel Synthesis of Differentially Substituted 5,7-Dialkoxyquinazolin-4-ones
Author:
Affiliation:
1. a Cancer and Infection Research , AstraZeneca Research and Developement , Alderley Park, U.K.
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397910802219247
Reference10 articles.
1. Small molecule tyrosine kinase inhibitors: clinical development of anticancer agents
2. Erlotinib: a new therapeutic approach for non-small cell lung cancer
3. Inhibitors of epidermal growth factor receptor tyrosine kinase: Novel C-5 substituted anilinoquinazolines designed to target the ribose pocket
4. New heterocyclic analogues of 4-(2-chloro-5-methoxyanilino)quinazolines as potent and selective c-Src kinase inhibitors
5. N-(5-Chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methylpiperazin-1-yl)ethoxy]-5- (tetrahydro-2H-pyran-4-yloxy)quinazolin-4-amine, a Novel, Highly Selective, Orally Available, Dual-Specific c-Src/Abl Kinase Inhibitor
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1. ChemInform Abstract: Novel Synthesis of Differentially Substituted 5,7-Dialkoxyquinazolin-4-ones.;ChemInform;2008-12-23
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