In our recent researches racemic RC-33 was identified as a potent and highly promising sigma1 receptor agonist, showing excellent sigma1 receptor affinity and promoting NGF-induced neurite outgrowth in PC12 cell at very low concentrations. Surprisingly, both its interaction with the biological target and its effect on neurite sprouting proved to be non-stereoselective. Starting from the observation that an hydrogen bond center in the scaffold of a sigma1 ligand is an important pharmacophoric element for receptor/ligand interaction, we hypothesized that the absence of such pharmacophoric feature in the structure of RC-33 could be also responsible for the lack of enantioselectivity in its interaction with the target receptor. To verify our hypothesis, in this paper we evaluated - both in silico and in vitro - the ability of a series of enantiomeric arylalkylaminoalcohols and arylpyrrolidinols 1-5 to interact with the receptor. All these compounds are structurally related to RC-33 and characterized by the presence of an –OH group as the additional pharmacophore feature. Interestingly, the results of our study shows that the sigma1 receptor exhibits enantiopreference toward compounds characterized by (S)-configuration at the stereogenic center bearing the aromatic moiety only when the alcoholic group is also present at that chiral center, thus supporting our original hypothesis.
A step forward in the sigma enigma: a role for chirality in the sigma1 receptor- ligand interaction?
ROSSI, DANIELA;MARRA, ANNAMARIA;RUI, MARTA;Marco Peviani;CURTI, DANIELA;COLLINA, SIMONA
2015-01-01
Abstract
In our recent researches racemic RC-33 was identified as a potent and highly promising sigma1 receptor agonist, showing excellent sigma1 receptor affinity and promoting NGF-induced neurite outgrowth in PC12 cell at very low concentrations. Surprisingly, both its interaction with the biological target and its effect on neurite sprouting proved to be non-stereoselective. Starting from the observation that an hydrogen bond center in the scaffold of a sigma1 ligand is an important pharmacophoric element for receptor/ligand interaction, we hypothesized that the absence of such pharmacophoric feature in the structure of RC-33 could be also responsible for the lack of enantioselectivity in its interaction with the target receptor. To verify our hypothesis, in this paper we evaluated - both in silico and in vitro - the ability of a series of enantiomeric arylalkylaminoalcohols and arylpyrrolidinols 1-5 to interact with the receptor. All these compounds are structurally related to RC-33 and characterized by the presence of an –OH group as the additional pharmacophore feature. Interestingly, the results of our study shows that the sigma1 receptor exhibits enantiopreference toward compounds characterized by (S)-configuration at the stereogenic center bearing the aromatic moiety only when the alcoholic group is also present at that chiral center, thus supporting our original hypothesis.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.