
pmid: 17127055
The synthesis of a series of carbazole derivatives and their SAR at the NPY Y1 receptor is described. Modulation of physicochemical properties by appropriate decoration led to the identification of a high-affinity NPY Y1 antagonist that shows high brain penetration and modest oral bioavailability.
Male, Chemical Phenomena, Chemistry, Physical, Carbazoles, Biological Availability, Brain, CHO Cells, Rats, Receptors, Neuropeptide Y, Rats, Sprague-Dawley, Structure-Activity Relationship, Cricetulus, Cricetinae, Animals, Indicators and Reagents, Half-Life
Male, Chemical Phenomena, Chemistry, Physical, Carbazoles, Biological Availability, Brain, CHO Cells, Rats, Receptors, Neuropeptide Y, Rats, Sprague-Dawley, Structure-Activity Relationship, Cricetulus, Cricetinae, Animals, Indicators and Reagents, Half-Life
| 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). | 19 | |
| 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. | Average | |
| 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% |
