| Literature DB >> 23806554 |
Amber Thaxton1, Sari Izenwasser, Dean Wade, Edwin D Stevens, David L Mobley, Vivian Jaber, Stacey A Lomenzo, Mark L Trudell.
Abstract
A series of 3-aryl-3-arylmethoxy-azetidines were synthesized and evaluated for binding affinities at dopamine and serotonin transporters. The 3-aryl-3-arylmethoxyazetidines were generally SERT selective with the dichloro substituted congener 7c (Ki=1.0 nM) and the tetrachloro substituted derivative 7i (Ki=1.3 nM) possessing low nanomolar affinity for the SERT. The 3-(3,4-dichlorophenyl-3-phenylmethoxyazetidine (7g) exhibited moderate affinity at both DAT and SERT transporters and suggests that substitution of the aryl rings can be used to tune the mononamine transporter affinity.Entities:
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Year: 2013 PMID: 23806554 PMCID: PMC3733996 DOI: 10.1016/j.bmcl.2013.05.071
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823