INVESTIGADORES
RADIVOY Gabriel Eduardo
congresos y reuniones científicas
Título:
Design, Synthesis, and Biological Assessment of Novel Vanillin-Isoxazole Derivatives as Positive Allosteric Modulators of Alfa-7 Nicotinic Acetylcholine Receptor
Autor/es:
S. STABILE; J. F. CHRESTIA; G. RADIVOY; C. BOUZAT
Reunión:
Congreso; 27th Electronic Conference on Synthetic Organic Chemistry (27th ECSOC); 2023
Resumen:
The homomeric α7 nicotinic acetylcholine receptor (α7 nAChR) is a cation-permeable pentameric ligand-gated channel present in the nervous system and in non-neuronal cells. α7 nAChRs are highly expressed in brain regions critical for cognition and memory, such as the hippocampus and cerebral cortex. Therefore, enhancing its function with positive allosteric modulators (PAMs) is a promising therapeutic approach for treating cognitive deficits and neurodegenerative disorders.Continuing with our previous work in the search for novel PAMs of α7 nAChR, this study presents the synthesis and biological evaluation of novel isoxazole-vanillin derivatives exhibiting α7-PAM activity. Isoxazole derivatives with functional α7-PAM activity were identified by determining the effects of the synthetic compounds at different concentrations on the properties of the single channels elicited by ACh (100 µM). We found that only vanillin-derived isoxazoles (containing the 4-hydroxy-3-methoxy fragment) exhibited α7-enhancing activity in comparison to isoxazoles derived from dihydroxy- or dimethoxybenzaldehydes. The use of different substituted phenylacetylenes allowed us to create a small library of compounds with α7-PAM activity.