Modified ibogaine fragments: synthesis and preliminary pharmacological characterization of 3-ethyl-5-phenyl-1,2,3,4,5, 6-hexahydroazepino[4,5-b]benzothiophenes.
Simon M. N. Efange, Deborah C. Mash, A B Khare, Q Ouyang
Journal of Medicinal Chemistry November 5, 1998 DOI: 10.1021/jm980156y (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Experimental study Qualitative Peer reviewed |
|---|---|
| Topics | Ibogaine Serotonin |
| Keywords | Drug discovery New compounds Novel compounds Synthesized Derivatives Fragments Medicinal chemistry Drug development Compound synthesis Addiction treatment Substance abuse therapy Addiction therapy Therapeutic applications Ibogaine research Neuropharmacology Dopamine transporters Serotonin transporters Dopamine d3 receptors Receptor binding Transporter modulation Neurotransmitter systems Potency |
| Citations | 33 |
| Key findings | All five phenyl-substituted derivatives of the ibogaine fragment displayed 8-10-fold higher affinity at the dopamine transporter than ibogaine and noribogaine. |
Abstract
Five phenyl-substituted derivatives and analogues of 1,2,3,4,5, 6-hexahydroazepino[4,5-b]indole, 5, a major fragment of ibogaine (1), were synthesized and tested for binding to monoamine transporters, the NMDA receptor-coupled cation channel, and dopamine and opioid receptors. All five derivatives, 9 and 17a-d, displayed 8-10-fold higher affinity at the DA transporter than ibogaine and noribogaine (4). At the serotonin transporter, two compounds (9 and 17a) exhibited higher potency than ibogaine, while the rest had weaker binding affinities than the lead compound. In keeping with their structural similarity to ibogaine, all five compounds displayed weak to poor affinity for dopamine D1 and D2 receptors. However, two compounds, 17a,c, demonstrated moderate binding affinities at dopamine D3 receptors. All five compounds displayed weak to poor affinities for mu and kappa opioid receptors and for the NMDA receptor-coupled cation channel. Despite the qualitative differences, derivatives and analogues of 5may serve as useful substitutes for ibogaine.