Potent BRAF kinase inhibitors based on 2,4,5-trisubstituted imidazole with naphthyl and benzothiophene 4-substituents. [electronic resource]
Producer: 20130823Description: 1284-304 p. digitalISSN:- 1464-3391
- Benzofurans -- chemistry
- Cell Line, Tumor
- Cell Survival -- drug effects
- Humans
- Imidazoles -- chemical synthesis
- Melanoma -- metabolism
- Naphthols -- chemical synthesis
- Protein Kinase Inhibitors -- chemical synthesis
- Proto-Oncogene Proteins B-raf -- antagonists & inhibitors
- Structure-Activity Relationship
- Thiophenes -- chemical synthesis
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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