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Ibogaine analogues. Synthesis and preliminary pharmacological evaluation of 7-heteroaryl-2-azabicyclo[2.2.2]oct-7-enes.

Daniele Passarella, Raffaele Favia, Alessandra Giardini, Giordano Lesma, Marisa Martinelli, Alessandra Silvani, Bruno Danieli, Simon M N Efange, Deborah C Mash

Bioorganic & medicinal chemistry March 20, 2003 DOI: 10.1016/s0968-0896(02)00524-2 via PubMed

Summary

AI-generated from the abstract

A method to synthesize 7-heteroaryl-2-azabicyclo[2.2.2]oct-7-enes using cycloaddition followed by cross-coupling is described. The binding affinity of these new compounds to the receptor targets characteristic of ibogaine is reported.

Study at a glance

Characteristics Theoretical or philosophical paper Peer reviewed
Citations 23
Key finding The synthesized compounds show binding affinity to the receptor targets characteristic of ibogaine.

Abstract

Synthesis of 7-heteroaryl-2-azabicyclo[2.2.2]oct-7-enes by cycloaddition and subsequent cross-coupling reaction is described. Binding affinity of these novel compounds towards the characteristic receptorial targets of ibogaine is illustrated.

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