| Literature DB >> 20694189 |
Qian-Sheng Yu1, Weiming Luo, Jeffery Deschamps, Harold W Holloway, Theresa Kopajtic, Jonathan L Katz, Arnold Brossi, Nigel H Greig.
Abstract
As a clinical medication for the treatment of hyperkinetic movement disorders, in conditions such as Huntington's disease, tetrabenazine (TBZ) has been always used in its racemic form. To establish whether or not its beneficial therapeutic actions are enantiospecific, a practical total synthetic route was developed to yield each enantiomeric form to allow their chemical and pharmacological characterization. We briefly summarize the total synthesis of TBZ and report a detailed procedure for resolution of TBZ into its enantiomers, (+)-TBZ and (-)-TBZ. This allowed determination of the optical rotation and absolute configurations of each TBZ enantiomer, based on X-ray crystallographic analysis, together with characterization of their inhibitory action at the vesicular monoamine transporter 2, where (+)-TBZ proved three-fold more active than (-)-TBZ.Entities:
Year: 2010 PMID: 20694189 PMCID: PMC2915582 DOI: 10.1021/ml1000189
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345