Synthesis and monoamine uptake inhibition of conformationally constrained 2β-carbomethoxy-3β-phenyl tropanes
作者:Patrick Johannes Riss、René Hummerich、Patrick Schloss
DOI:10.1039/b902863c
日期:——
A series of 2β-carbomethoxy-3β-phenyl tropanes with conformationally constrained nitrogen substituents were synthesized as potential selective dopamine transporter ligands. These novel compounds were examined for their monoamine uptake inhibition potency at the human dopamine transporter (hDAT), the human serotonin transporter (hSERT) and the human noradrenalin transporter (hNET), stably expressed
合成了一系列具有构象约束的氮取代基的2β-羰甲氧基-3β-苯基托烷,作为潜在的选择性 多巴胺转运体配体。对这些新型化合物进行了检查一元胺 对人体的吸收抑制能力 多巴胺 运输者(hDAT), 人类 血清素 运输者(hSERT)和人类 去甲肾上腺素 运输者(网络),在人类胚胎肾细胞(HEK)中稳定表达。进行了SAR研究,以确定在C链上延伸的,4-氟化,构象受限的C 4链的贡献。托烷 氮对人 一元胺 转运蛋白的亲和力和选择性。