Synthesis and Biological Evaluation of Novel Compounds within a Class of 3-Aminochroman Derivatives with Dual 5-HT<sub>1A</sub> Receptor and Serotonin Transporter Affinity
作者:Nicole T. Hatzenbuhler、Deborah A. Evrard、Boyd L. Harrison、Donna Huryn、Jennifer Inghrim、Christina Kraml、James F. Mattes、Richard E. Mewshaw、Dahui Zhou、Geoffrey Hornby、Qian Lin、Deborah L. Smith、Kelly M. Sullivan、Lee E. Schechter、Chad E. Beyer、Terrance H. Andree
DOI:10.1021/jm060218h
日期:2006.7.1
Compounds containing a 5-carbamoyl-8-fluoro-3-amino-3,4-dihydro-2H-1-benzopyran and a 3-alkylindole moiety linked through a common basic nitrogen were prepared and evaluated for 5-HT1A affinity, serotonin rat transporter affinity, and functional antagonist activity in vitro. 26a was found to be the most potent and selective compound in this series and was shown to possess neurochemical activity in vivo by
制备了包含5-氨基甲酰基-8-氟-3-氨基-3,4-二氢-2H-1-苯并吡喃和通过共同碱性氮连接的3-烷基吲哚部分的化合物并评估了5-HT1A亲和力转运蛋白亲和力和体外功能拮抗剂活性。已发现26a是该系列中最有效和最具选择性的化合物,并通过在大鼠额叶皮层中产生5-HT急剧且快速的增加而显示其在体内具有神经化学活性。