Synthesis and Biological Evaluation of Rigid Analogues of Methamphetamines

<p>A series of rigid azetidenyl-based methamphetamine analogs were synthesized from commercially available <em>N</em>-Boc-azetidinone. The benzylideneazetidine analogs were prepared via a Wittig olefination via the ylides generated from the corresponding triphenylphosphonium benzylhalide salts. The substituted benzylazetidine analogs were synthesized from the corresponding benzylideneazetidienes via hydrogention over palladium and platinum catalysts. The benzylideneazetidine and benzyliazetidine analogs were evaluated at monoamine transporters as a part of preliminary structure-activity study for the development of novel monoamine transporter ligands. The binding affinities of the azetidine analogs were determined at dopamine (DAT) and serotonin (SERT) transporters in rat brain tissue preparations. The preliminary in vitro binding studies revealed that the rigid scaffold of the azetidine ring system was an effective substitution for the 2-aminopropyl group of methamphetamine and led to compounds with nanomolar binding affinity at dopamine and serotonin. In general, the benzylideneazetidine analogs were more potent than the corresponding benzylazetidine analogs. In addition, the azetidine analogs were more selective for the serotonin transporter than the dopamine transporter. The 3-(3,4-dichlorobenzylidene)azetidine (<strong>24m</strong>) was the most potent analog of the series with K_i values of 139 nM for SERT and 531 nM for DAT (DAT/SERT = 3.8).</p>

Name thesis:degree_name

Ph.D.

Level thesis:degree_level

Dissertation

Discipline thesis:degree_discipline

Chemistry

Year

2012

Author dc:creator

• Forsyth, Andrea N

Contributors dc:contributor

• Mark Trudell
• Guijun Wang
• David Mobley

• dopamine, serotonin, norepinephrine, azetidine, psychostimulant, amphetamine, methamphetamine
• Medicinal-Pharmaceutical Chemistry
• Organic Chemistry

Repository record dc:identifier

https://scholarworks.uno.edu/td/1436

OAI identifier oai:identifier

oai:scholarworks.uno.edu:td-2429