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1-(芳基)-6-[烷氧基烷基]-3-氮杂双环[3.1.0]己烷和 6-(芳基)-6-[烷氧基烷基]-3-氮杂双环[3.1.0]己烷:一类新型强效和高选择性三重再摄取抑制剂。

1-(Aryl)-6-[alkoxyalkyl]-3-azabicyclo[3.1.0]hexanes and 6-(aryl)-6-[alkoxyalkyl]-3-azabicyclo[3.1.0]hexanes: a new series of potent and selective triple reuptake inhibitors.

机构信息

Neurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline Medicine Research Centre, Via Fleming 4, 37135 Verona, Italy.

出版信息

J Med Chem. 2010 Mar 25;53(6):2534-51. doi: 10.1021/jm901818u.

Abstract

The discovery of new highly potent and selective triple reuptake inhibitors is reported. The new classes of 1-(aryl)-6-[alkoxyalkyl]-3-azabicyclo[3.1.0]hexanes and 6-(aryl)-6-[alkoxyalkyl]-3-azabicyclo[3.1.0]hexanes are described together with detailed SAR. Appropriate decoration of the scaffolds was achieved with the help of a triple reuptake inhibitor pharmacophore model detailed here. Selected derivatives showed good oral bioavailability (>30%) and brain penetration (B/B > 4) in rats associated with high in vitro potency and selectivity at SERT, NET, and DAT. Among these compounds, microdialysis and in vivo experiments confirm that derivative 15 has an appropriate developability profile to be considered for further progression.

摘要

报告了新的高活性和选择性三重再摄取抑制剂的发现。新的 1-(芳基)-6-[烷氧基烷基]-3-氮杂双环[3.1.0]己烷类和 6-(芳基)-6-[烷氧基烷基]-3-氮杂双环[3.1.0]己烷类化合物以及详细的 SAR 一起被描述。在详细阐述的三重再摄取抑制剂药效团模型的帮助下,适当修饰了支架。选择的衍生物在大鼠中具有良好的口服生物利用度(>30%)和脑穿透性(B/B>4),并具有高体外 SERT、NET 和 DAT 活性和选择性。在这些化合物中,微透析和体内实验证实,衍生物 15 具有适当的可开发性特征,可考虑进一步推进。

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