Micheli Fabrizio, Bonanomi Giorgio, Blaney Frank E, Braggio Simone, Capelli Anna Maria, Checchia Anna, Curcuruto Ornella, Damiani Federica, Fabio Romano Di, Donati Daniele, Gentile Gabriella, Gribble Andy, Hamprecht Dieter, Tedesco Giovanna, Terreni Silvia, Tarsi Luca, Lightfoot Andrew, Stemp Geoff, Macdonald Gregor, Smith Alex, Pecoraro Michela, Petrone Marcella, Perini Ornella, Piner Jacqui, Rossi Tino, Worby Angela, Pilla Maria, Valerio Enzo, Griffante Cristiana, Mugnaini Manolo, Wood Martyn, Scott Claire, Andreoli Michela, Lacroix Laurent, Schwarz Adam, Gozzi Alessandro, Bifone Angelo, Ashby Charles R, Hagan Jim J, Heidbreder Christian
Psychiatry Centre of Excellence, Molecular Discovery Research, and Safety Assessment, GlaxoSmithKline Medicine Research Centre, Via Fleming 4, 37135 Verona, Italy.
J Med Chem. 2007 Oct 18;50(21):5076-89. doi: 10.1021/jm0705612. Epub 2007 Sep 15.
The discovery of new highly potent and selective dopamine D3 receptor antagonists has recently permitted characterization of the role of the dopamine D3 receptor in a wide range of preclinical animal models. A novel series of 1,2,4-triazol-3-yl-thiopropyl-tetrahydrobenzazepines demonstrating a high level of D3 affinity and selectivity with an excellent pharmacokinetic profile is reported here. In particular, the pyrazolyl derivative 35 showed good oral bioavailability and brain penetration associated with high potency and selectivity in vitro. In vivo characterization of 35 confirmed that this compound blocks the expression of nicotine- and cocaine-conditioned place preference in the rat, prevents nicotine-triggered reinstatement of nicotine-seeking behavior in the rat, reduces oral operant alcohol self-administration in the mouse, increases extracellular levels of acetylcholine in the rat medial prefrontal cortex, and potentiates the amplitude of the relative cerebral blood volume response to d-amphetamine in a regionally specific manner in the rat brain.
最近,新型高效且选择性的多巴胺D3受体拮抗剂的发现,使得在多种临床前动物模型中能够对多巴胺D3受体的作用进行表征。本文报道了一系列新型的1,2,4-三唑-3-基-硫代丙基-四氢苯并氮杂䓬,它们表现出高水平的D3亲和力和选择性,且具有优异的药代动力学特征。特别地,吡唑基衍生物35在体外表现出高效力和选择性的同时,还具有良好的口服生物利用度和脑渗透性。对35的体内表征证实,该化合物可阻断大鼠中尼古丁和可卡因条件性位置偏爱行为的表达,防止大鼠中尼古丁引发的尼古丁寻求行为的恢复,减少小鼠口服操作性酒精自我给药,增加大鼠内侧前额叶皮质中乙酰胆碱的细胞外水平,并以区域特异性方式增强大鼠脑中对d-苯丙胺的相对脑血容量反应的幅度。