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Quinlobelane: a water-soluble lobelane analogue and inhibitor of VMAT2.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2010 Jun 15; Vol. 20 (12), pp. 3584-7. Date of Electronic Publication: 2010 May 04. - Publication Year :
- 2010
-
Abstract
- Replacing the phenyl groups in the structure of the VMAT2 inhibitor, lobelane with either pyridyl, quinolyl or indolyl groups affords novel analogues with improved water solubility. The synthetic methodologies reported herein also underscore the paucity of hydrogenation methods that offer selectivity in the synthesis of the different classes of heteroaromatic lobelane analogues. The quinolyl group was the only replacement for the phenyl group in lobelane that retained VMAT2 inhibition.<br /> (Copyright 2010 Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Binding Sites
Dopamine pharmacokinetics
Humans
Hydrogenation
Hydroquinones
Lobelia
Lobeline chemical synthesis
Lobeline pharmacology
Methamphetamine
Solubility
Structure-Activity Relationship
Substance-Related Disorders drug therapy
Synaptic Vesicles metabolism
Lobeline analogs & derivatives
Vesicular Monoamine Transport Proteins antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3405
- Volume :
- 20
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 20494575
- Full Text :
- https://doi.org/10.1016/j.bmcl.2010.04.117