Design, synthesis and structure-activity relationships of novel strychnine-insensitive glycine receptor ligands
作者:A. Cordi、J.-M. Lacoste、V. Audinot、M. Millan
DOI:10.1016/s0960-894x(99)00194-8
日期:1999.5
The in vitro activities of 3-hydroxy-imidazolidin-4-one derivatives demonstrated very restricted structure-activity relationships at the strychnine-insensitive glycine site of the NMDA receptor. The most active compound (3a) was completely unsubstituted and exhibited affinity and efficacy similar to that of D-cycloserine, the prototypical partial agonist at this site. (C) 1999 Elsevier Science Ltd. All rights reserved.
Design of metal chelates with biological activity. 3. Nickel(II) complexes of alkyl and amino hydroxamic acids