New fused benzazepine as selective D3 receptor antagonists. Synthesis and biological evaluation. Part one: [h]-fused tricyclic systems
作者:Fabrizio Micheli、Giorgio Bonanomi、Simone Braggio、Anna Maria Capelli、Paolo Celestini、Federica Damiani、Romano Di Fabio、Daniele Donati、Stefania Gagliardi、Gabriella Gentile、Dieter Hamprecht、Marcella Petrone、Stefano Radaelli、Giovanna Tedesco、Silvia Terreni、Angela Worby、Christian Heidbreder
DOI:10.1016/j.bmcl.2007.12.066
日期:2008.2
The synthesis and SAR of a new series of potent and selective dopamine D(3) receptor antagonists is reported. The introduction of a tricyclic [h]-fused benzazepine moiety on the recently disclosed scaffold of 1,2,4-triazol-3-yl-thiopropyl-tetrahydrobenzazepines is reported. A full rat pharmacokinetic characterization is also reported.
合成和SAR的一系列新的有效和选择性多巴胺D(3)受体拮抗剂的报道。据报道,在最近公开的1,2,4-三唑-3-基-硫丙基-四氢苯并ze庚因的支架上引入了三环[h]-稠合的苯并ze庚因部分。还报道了完整的大鼠药代动力学特征。