4,4-Dimethyl- and diastereomeric 4-hydroxy-4-methyl-(2S)-glutamate analogues display distinct pharmacological profiles at ionotropic glutamate receptors and excitatory amino acid transporters

Research output: Contribution to journalJournal articleResearchpeer-review

Lennart Bunch, Darryl S Pickering, Thierry Gefflaut, Virginie Vinatier, Virgil Helaine, Ahmad Amir, Birgitte Nielsen, Anders Asbjørn Jensen

Subtype-selective ligands are of great interest to the scientific community, as they provide a tool for investigating the function of one receptor or transporter subtype when functioning in its native environment. Several 4-substituted (S)-glutamate (Glu) analogues were synthesized, and altogether this approach has provided important insight into the structure-activity relationships (SAR) for ionotropic and metabotropic glutamate receptors (iGluRs and mGluRs), as well as the excitatory amino acid transporters (EAATs). In this work, three 4,4-disubstituted Glu analogues 1-3, which are hybrid structures of important 4-substituted Glu analogues 4-8, were investigated at iGluRs and EAATs. Collectively, their pharmacological profiles add new and valuable information to the SAR for the iGluRs and EAAT1-3.
Original languageEnglish
JournalChemMedChem
Volume4
Issue number11
Pages (from-to)1925-1929
ISSN1860-7179
DOIs
Publication statusPublished - 2009

ID: 17007204