化学
氯氮平
选择性
立体化学
多巴胺受体D2
化学合成
药理学
受体
体外
精神分裂症(面向对象编程)
生物化学
计算机科学
医学
催化作用
程序设计语言
作者
Thomas Hussenether,Harald Hübner,Peter Gmeiner,Reinhard Troschütz
标识
DOI:10.1016/j.bmc.2004.03.023
摘要
Novel 4-arylpiperazin-1-yl-substituted 2,3-dihydro-1H-1,4- and 1H-1,5-benzodiazepines and their aza-analogues were synthesized as debenzoclozapine derivatives for evaluation as potential D4-ligands. While Ki values of some of the title compounds came within the range of clozapine, they showed an impressively greater selectivity over other dopamine receptor subtypes, especially D2. For the most promising compounds, intrinsic activity and binding properties to serotonin 5-HT1A and 5-HT2 were also determined.
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