
pmid: 17010607
A series of xanthine mimetics containing 5,5 and 5,6 heterocycle fused imidazoles were synthesized as dipeptidyl peptidase IV inhibitors. Compound 7 is potent (h-DPPIV K(i)=2nM) and exhibits excellent selectivity and no species specificity against rat and human enzymes. The X-ray structure confirms that the binding mode of 7 to rat DPPIV is similar to the parent xanthines.
Models, Molecular, Dipeptidyl-Peptidase IV Inhibitors, Protein Conformation, Dipeptidyl Peptidase 4, Imidazoles, Rats, Kinetics, Structure-Activity Relationship, X-Ray Diffraction, Xanthines, Animals, Protease Inhibitors
Models, Molecular, Dipeptidyl-Peptidase IV Inhibitors, Protein Conformation, Dipeptidyl Peptidase 4, Imidazoles, Rats, Kinetics, Structure-Activity Relationship, X-Ray Diffraction, Xanthines, Animals, Protease Inhibitors
| 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). | 20 | |
| 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). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
