| Literature DB >> 31986621 |
Alexandra Dassonville-Klimpt1, Christine Cézard1, Catherine Mullié1, Patrice Agnamey1, Alexia Jonet1, Sophie Da Nascimento1, Mathieu Marchivie2, Jean Guillon2, Pascal Sonnet1.
Abstract
Mefloquine (MQ), an antimalarial drug, is used as a racemate of (-)- and (+)-enantiomers, which display biological differences. The question concerning their exact configuration remains a matter of debate. The absolute configuration of the two MQ enantiomers as well as their biological activity has been established, thus confirming the importance of the stereochemistry in the design of MQ analogues that have fewer adverse side effects.Entities:
Keywords: absolute configuration; antimalarial activity; enantiomers; erythro-mefloquine; stereoselectivity; structure elucidation
Year: 2013 PMID: 31986621 DOI: 10.1002/cplu.201300074
Source DB: PubMed Journal: Chempluschem ISSN: 2192-6506 Impact factor: 2.863