Synthesis and biological activity of 5-chloro-N4-substituted phenyl-9H-pyrimido[4,5-b]indole-2,4-diamines as vascular endothelial growth factor receptor-2 inhibitors and antiangiogenic agents
- 1 April 2013
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry
- Vol. 21 (7) , 1857-1864
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Receptor-Based Virtual Screening of EGFR Kinase Inhibitors from the NCI Diversity DatabaseMolecules, 2010
- Single Agents with Designed Combination Chemotherapy Potential: Synthesis and Evaluation of Substituted Pyrimido[4,5-b]indoles as Receptor Tyrosine Kinase and Thymidylate Synthase Inhibitors and as Antitumor AgentsJournal of Medicinal Chemistry, 2010
- Selectively Nonselective Kinase Inhibition: Striking the Right BalanceJournal of Medicinal Chemistry, 2009
- NilotinibClinical Cancer Research, 2008
- The Role of VEGF and EGFR Inhibition: Implications for Combining Anti–VEGF and Anti–EGFR AgentsMolecular Cancer Research, 2007
- Lapatinib: A novel EGFR/HER2 tyrosine kinase inhibitor for cancerDrugs of Today, 2006
- Role of Tyrosine Kinase Inhibitors in Cancer TherapyThe Journal of Pharmacology and Experimental Therapeutics, 2005
- Novel 4-amino-furo[2,3-d]pyrimidines as Tie-2 and VEGFR2 dual inhibitorsBioorganic & Medicinal Chemistry Letters, 2005
- The discovery of receptor tyrosine kinases: targets for cancer therapyNature Reviews Cancer, 2004
- The biology of VEGF and its receptorsNature Medicine, 2003