Our recent research efforts identified racemic RC-33 as a potent and metabolically stable s1 receptor agonist. Herein we describe the isolation of pure RC-33 enantiomers by chiral chromatography, assignment of their absolute configuration, and in vitro biological studies in order to address the role of chirality in the biological activity of these compounds and their metabolic processing. The binding of enantiopure RC-33 to the s1 receptor was also investigated in silico by molecular dynamics simulations. Both RC-33 enantiomers showed similar affinities for the s1 receptor and appeared to be almost equally effective as s1 receptor agonists. However, the R-configured enantiomer showed higher in vitro hepatic metabolic stability in the presence of NADPH than the S enantiomer. Overall, the results presented herein led us to select (R)-RC-33 as the optimal candidate for further in vivo studies in an animal model of amyotrophic lateral sclerosis.
|Titolo:||Chemical, Pharmacological, and in vitro Metabolic Stability Studies on Enantiomerically Pure RC-33 Compounds: Promising Neuroprotective Agents Acting as σ1 Receptor Agonists|
|Parole Chiave:||σ1 agonists.; Biological activity; Enantioselectivity; In vitro metabolism; Neuroprotective agents|
|Settore Scientifico Disciplinare:||Settore CHIM/06 - Chimica Organica|
Settore BIO/10 - Biochimica
|Data di pubblicazione:||5-lug-2013|
|Digital Object Identifier (DOI):||10.1002/cmdc.201300218|
|Appare nelle tipologie:||01 - Articolo su periodico|