Stereochemistry
Reproterol contains a stereocenter and is chiral . There are thus two enantiomers , the (R )-form and the (S )-form. The commercial preparations contain the drug as a racemate , an equal mixture of the two enantiomers.[ 4]
Enantiomers of reproterol
(R )-Reproterol CAS number: 210710-33-1
(S )-Reproterol CAS number: 210710-34-2
References
↑ Küpper T, Goebbels K, Kennes LN, Netzer NC (December 2012). "Cromoglycate, reproterol, or both--what's best for exercise-induced asthma?". Sleep & Breathing = Schlaf & Atmung . 16 (4): 1229– 35. doi :10.1007/s11325-011-0638-2 . PMID 22198635 . S2CID 10032756 .
↑ Virchow JC (1999). "Reproterol: beta-2-agonist, theophylline, or both?". Respiration; International Review of Thoracic Diseases . 66 (3): 210– 1. doi :10.1159/000029379 . PMID 10364735 . S2CID 203732706 .
↑ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery . John Wiley & Sons. p. 54X. ISBN 9783527607495 .
↑ Rote Liste 2017 – Arzneimittelverzeichnis für Deutschland (einschließlich EU-Zulassungen und bestimmter Medizinprodukte) . Vol. 57. Frankfurt/Main: Rote Liste Service GmbH. 2017. p. 196. ISBN 978-3-946057-10-9 .
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