A new structurally simple series of potent lipophilic aza-retinoids RXR agonists has been developed. SAR studies for the N-alkyl-azadienoic acids described here demonstrate that the RXR activity profile is sensitive to the N-alkyl chain length. Further, we have expanded the work to include azadienoic acids, which exhibited many accessible conformations leading to a better understanding of the SAR around
已经开发了一系列新的结构简单的有效亲脂性氮杂-类
维生素A RXR激动剂。此处描述的N-烷基-氮杂二烯酸的
SAR研究表明,RXR活性谱对N-烷基链长敏感。此外,我们将工作扩展到了氮杂二烯酸,其显示出许多可及的构象,从而使人们对该系列的
SAR有更好的了解。