Design and synthesis of 5,6-fused heterocyclic amides as Raf kinase inhibitors
- Resource Type
- Source
- Bioorganic & Medicinal Chemistry Letters. 21:3286-3289
- Subject
Models, Molecular Binding Sites Molecular Structure Chemistry Stereochemistry Organic Chemistry Clinical Biochemistry Pharmaceutical Science Raf kinase Amides Biochemistry In vitro Enzyme Activation Structure-Activity Relationship Heterocyclic Compounds Drug Design Drug Discovery Molecular Medicine raf Kinases Enzyme Inhibitors Molecular Biology Cell Proliferation - Language
- ISSN
- 0960-894X