A series of novel indole-based analogs were prepared and their affinities for sigma receptors were determined using in vitro radioligand binding assays. The results of this study identified several compounds with nanomolar sigma-2 affinity and significant selectivity over sigma-1 receptors. In particular, 2-(4-(3-(4-fluorophenyl)indol-1-yl)butyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (9f) was found to display high affinity at sigma-2 receptors with good selectivity (Ï-1/Ï-2 = 395). The pharmacological binding profile for this compound was established with other relevant non-sigma sites.
Synthesis and pharmacological evaluation of indole-based sigma receptor ligands.
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作者:Mésangeau Christophe, Amata Emanuele, Alsharif Walid, Seminerio Michael J, Robson Matthew J, Matsumoto Rae R, Poupaert Jacques H, McCurdy Christopher R
| 期刊: | European Journal of Medicinal Chemistry | 影响因子: | 5.900 |
| 时间: | 2011 | 起止号: | 2011 Oct;46(10):5154-61 |
| doi: | 10.1016/j.ejmech.2011.08.031 | ||
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