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Chem Commun (Camb) ; 52(85): 12582-12585, 2016 Oct 18.
Article in English | MEDLINE | ID: mdl-27722284

ABSTRACT

Administration of enantiomerically pure ß-adrenergic agonists and antagonists increases their activity and reduces side effects. We report here a small-molecule artificial receptor (SMAR) that, by mimicking the ß-adrenergic receptor, is able to enantioselectively extract commercial ß-adrenergic interacting drugs. The selectivity is justified according to DFT calculations and X-ray diffraction experiments.


Subject(s)
Adrenergic beta-Agonists/pharmacology , Adrenergic beta-Antagonists/pharmacology , Receptors, Adrenergic, beta/chemistry , Receptors, Artificial/metabolism , Humans , Quantum Theory , Stereoisomerism
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