作者:Michael A. Letavic、John M. Keith、Kiev S. Ly、Pascal Bonaventure、Mark A. Feinstein、Brian Lord、Kirsten L. Miller、S. Timothy Motley、Diane Nepomuceno、Steven W. Sutton、Nicholas I. Carruthers
DOI:10.1016/j.bmcl.2008.09.077
日期:2008.11
The synthesis and biological activity of a new series of 2-aryloxymethylmorpholine histamine H(3) antagonists is described. The new compounds are high affinity histamine H(3) ligands that penetrate the CNS and occupy the histamine H(3) receptor in rat brain.
合成和生物活性的新系列的2-芳氧基甲基吗啉组胺H(3)拮抗剂。新化合物是高亲和力组胺H(3)配体,可穿透CNS并占据大鼠脑中的组胺H(3)受体。