| Literature DB >> 12166935 |
Iván Collado1, Concepción Pedregal, Angel Mazón, Juan Félix Espinosa, Jaime Blanco-Urgoiti, Darryle D Schoepp, Rebecca A Wright, Bryan G Johnson, Ann E Kingston.
Abstract
The asymmetric synthesis and biological activity of (2S,1'S,2'S,3'R)-2-(2'-carboxy-3'-methylcyclopropyl) glycine 7 and its epimer at the C3' center 6 are described. Compound 7 is a highly potent and selective agonist for group 2 metabotropric glutamate receptors (mGluRs). It is also systemically 4 orders of magnitude more active in the fear-potentiated startle model of anxiety in rats than the rigid constrained bicyclic system LY354740. Therefore, we have shown that high molecular complexity of conformationally constrained bicyclic systems is not a requirement to achieve highly selective and potent group 2 mGluRs agonists.Entities:
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Year: 2002 PMID: 12166935 DOI: 10.1021/jm0110486
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446