Abstract
It is well known that many medicines are a mixture of two enantiomers, or mirror-image molecules. Two enantiomers occur when a molecule has a single chiral centre and the two mirror images, called S or L (left handed) and R or D (right handed), are usually found in equal amounts in the parent (racemic) mixture. While for many compounds used in clinical practice the active moiety is found in one of the two enantiomers with the other being seen as an unnecessary and redundant component of the racemic mixture, the difference between enantiomers can mean a difference between therapeutic and adverse effects, as well as in beneficial pharmacological effect and potency.
| Original language | English |
|---|---|
| Pages (from-to) | 1137-1141 |
| Number of pages | 5 |
| Journal | Journal of Psychopharmacology |
| Volume | 24 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - Aug 2010 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- Citalopram
- enantiomers
- escitalopram
- eszopiclone
- fluoxetine
- zopiclone
Fingerprint
Dive into the research topics of 'What one hand giveth the other taketh away: some unpredicted effects of enantiomers in psychopharmacology'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver