부산대학교 도서관

Replacement of the methyl group of the AMPA receptor agonist 2-amino-3-3-hydroxy-5-(2-methyl-2H-5-tetrazolyl)-4-isoxazolylpropionic acid (2-Me-Tet-AMPA) with a benzyl group provided the first AMPA receptor agonist, compound 7, capable of discriminating GluR2−4 from GluR1 by its more than 10-fold preference for the former receptor subtypes. An X-ray crystallographic analysis of this new analogue in complex with the GluR2-S1S2J construct shows that accommodation of the benzyl group creates a previously unobserved pocket in the receptor, which may explain the remarkable pharmacological profile of compound 7. [ABSTRACT FROM AUTHOR]