
A novel imidazo-pyramidazine inhibitor of DAPK1 that undergoes class-specific interactions and extends into the substrate recognition site has been identified. This inhibitor is a good starting point for the development of selective and potent inhibitors of DAPK1, with potential use against stroke and ischemia.
Models, Molecular, Molecular Sequence Data, Microfluidic Analytical Techniques, Crystallography, X-Ray, Ligands, Receptors, N-Methyl-D-Aspartate, Communications, High-Throughput Screening Assays, Pyridazines, Death-Associated Protein Kinases, Kinetics, Gene Expression Regulation, Catalytic Domain, Benzamides, Humans, Amino Acid Sequence, Phosphorylation, Protein Kinase Inhibitors, Enzyme Assays, Protein Binding
Models, Molecular, Molecular Sequence Data, Microfluidic Analytical Techniques, Crystallography, X-Ray, Ligands, Receptors, N-Methyl-D-Aspartate, Communications, High-Throughput Screening Assays, Pyridazines, Death-Associated Protein Kinases, Kinetics, Gene Expression Regulation, Catalytic Domain, Benzamides, Humans, Amino Acid Sequence, Phosphorylation, Protein Kinase Inhibitors, Enzyme Assays, Protein Binding
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 24 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
