Synthesis and Biological Evaluation of an Indomethacin Library Reveals a New Class of Angiogenesis‐Related Kinase Inhibitors
- 19 December 2003
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 43 (2) , 224-228
- https://doi.org/10.1002/anie.200352582
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Development of Natural Product-Derived Receptor Tyrosine Kinase Inhibitors Based on Conservation of Protein Domain FoldJournal of Medicinal Chemistry, 2003
- The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged SubstructuresChemical Reviews, 2003
- Protein kinases — the major drug targets of the twenty-first century?Nature Reviews Drug Discovery, 2002
- The “Resin-Capture-Release” Hybrid Technique: A Merger between Solid- and Solution-Phase SynthesisChemistry – A European Journal, 2000
- New Anilinophthalazines as Potent and Orally Well Absorbed Inhibitors of the VEGF Receptor Tyrosine Kinases Useful as Antagonists of Tumor-Driven AngiogenesisJournal of Medicinal Chemistry, 2000
- Small molecule inhibitors of receptor tyrosine kinasesDrugs of the Future, 1999
- Integrin Antagonists and Other Low Molecular Weight Compounds as Inhibitors of Angiogenesis: New Drugs in Cancer TherapyAngewandte Chemie International Edition in English, 1997
- Integrinantagonisten und andere niedermolekulare Verbindungen als Inhibitoren der Angiogenese ‐ neue Wirkstoffe in der TumortherapieAngewandte Chemie, 1997
- Aspirin therapy for cardiovascular diseaseCurrent Opinion in Hematology, 1996
- Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonistsJournal of Medicinal Chemistry, 1988