The synthesis of four new isoxazoline-based amino acids being analogues of previously described glutamate receptor ligands is reported and their affinity for ionotropic glutamate receptors is analyzed in comparison with that of selected model compounds. Molecular modelling investigations have been carried out to rationalize the interaction with the NMDA receptors.

Synthesis of new isoxazoline-based acidic amino acids and investigation of their affinity and selectivity profile at ionotropic glutamate receptors / A. Pinto, P. Conti, G. Grazioso, L. Tamborini, U. Madsen, B. Nielsen, C. De Micheli. - In: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY. - ISSN 0223-5234. - 46:2(2011), pp. 787-793. [10.1016/j.ejmech.2010.12.020]

Synthesis of new isoxazoline-based acidic amino acids and investigation of their affinity and selectivity profile at ionotropic glutamate receptors

A. Pinto
Primo
;
P. Conti
Secondo
;
G. Grazioso;L. Tamborini;C. De Micheli
Ultimo
2011

Abstract

The synthesis of four new isoxazoline-based amino acids being analogues of previously described glutamate receptor ligands is reported and their affinity for ionotropic glutamate receptors is analyzed in comparison with that of selected model compounds. Molecular modelling investigations have been carried out to rationalize the interaction with the NMDA receptors.
1,3-Dipolar cycloaddition; Glutamic acid; Ionotropic Glu receptors; Isoxazoline
Settore CHIM/08 - Chimica Farmaceutica
2011
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/151023
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