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探索双重 5-羟色胺转运体再摄取抑制剂-组胺 H3 受体拮抗剂的构效关系。

Exploration of structure-activity relationships for dual serotonin transporter reuptake inhibitors-histamine H3 receptor antagonists.

机构信息

Johnson & Johnson Pharmaceutical Research and Development L.L.C., San Diego, CA 92121, USA.

出版信息

Curr Top Med Chem. 2010;10(5):596-616. doi: 10.2174/156802610791111515.

Abstract

Depression is a major health issue, which is routinely treated with selective serotonin reuptake inhibitors. However, although these agents display a favorable effect on mood, they often fail to improve conditions that accompany depression including cognitive impairment and fatigue. In pre-clinical studies histamine H(3) receptor antagonists have demonstrated both pro-cognitive and wake-promoting effects suggesting that the combination of a histamine H(3) receptor antagonist and a serotonin reuptake inhibitor may have utility as an antidepressant therapy. To this end we sought to introduce histamine H(3) receptor antagonist activity into both known selective serotonin reuptake inhibitors and novel templates. These efforts have afforded several series of compounds with the desired activities. Selected examples demonstrated in vivo efficacy both in pre-clinical models of depression and wakefulness.

摘要

抑郁症是一个主要的健康问题,通常采用选择性 5-羟色胺再摄取抑制剂(SSRIs)进行治疗。然而,尽管这些药物在改善情绪方面显示出良好的效果,但它们往往无法改善伴随抑郁症的情况,包括认知障碍和疲劳。在临床前研究中,组胺 H(3)受体拮抗剂已显示出认知促进和觉醒促进作用,这表明组胺 H(3)受体拮抗剂与 5-羟色胺再摄取抑制剂的联合使用可能作为一种抗抑郁治疗具有实用性。为此,我们试图在已知的选择性 5-羟色胺再摄取抑制剂和新型模板中引入组胺 H(3)受体拮抗剂活性。这些努力提供了具有所需活性的几个系列化合物。选定的实例在抑郁症和觉醒的临床前模型中均显示出体内疗效。

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