Synthesis and Structure Activity Relationship of Tetrahydroisoquinoline-Based Potentiators of GluN2C and GluN2D Containing N‑Methyl‑d‑aspartate Receptors

• Published in: Journal of medicinal chemistry Vol. 56; no. 13; pp. 5351 - 5381
• Main Authors: Santangelo Freel, Rose M, Ogden, Kevin K, Strong, Katie L, Khatri, Alpa, Chepiga, Kathryn M, Jensen, Henrik S, Traynelis, Stephen F, Liotta, Dennis C
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 11.07.2013; Amer Chemical Soc
• Subjects: Animals; Cell Line; Chemistry, Medicinal; Excitatory Amino Acid Agonists - chemical synthesis; Excitatory Amino Acid Agonists - pharmacology; Female; Glutamic Acid - pharmacology; Glycine - pharmacology; Life Sciences & Biomedicine; Membrane Potentials - drug effects; Models, Chemical; Molecular Structure; Oocytes - drug effects; Oocytes - metabolism; Oocytes - physiology; Pharmacology & Pharmacy; Protein Subunits - agonists; Protein Subunits - genetics; Protein Subunits - metabolism; Rats; Receptors, N-Methyl-D-Aspartate - agonists; Receptors, N-Methyl-D-Aspartate - genetics; Receptors, N-Methyl-D-Aspartate - metabolism; Science & Technology; Structure-Activity Relationship; Tetrahydroisoquinolines - chemical synthesis; Tetrahydroisoquinolines - chemistry; Tetrahydroisoquinolines - pharmacology; Xenopus laevis; ALLOSTERIC MODULATORS; BRAIN-INJURY; RECOMBINANT; NR2B SUBUNIT; D-CYCLOSERINE; CHIRAL IMINIUM IONS; GLYCINE-BINDING; NR1/NR2C NMDA RECEPTORS; NONCOMPETITIVE INHIBITION; CHANNEL BLOCKERS
• ISSN: 0022-2623; 1520-4804
• DOI: 10.1021/jm400177t

We describe here the synthesis and evaluation of a series of tetrahydroisoquinolines that show subunit-selective potentiation of NMDA receptors containing the GluN2C or GluN2D subunits. Bischler–Napieralski conditions were employed in the key step for the conversion of acyclic amides to the corresponding tetrahydroisoquinoline-containing analogs. Compounds were evaluated using both two-electrode voltage clamp recordings from Xenopus laevis oocytes and imaging of mammalian BHK cells loaded with Ca2+-sensitive dyes. The most potent analogues had EC50 values of 300 nM and showed over 2-fold potentiation of the response to maximally effective concentrations of glutamate and glycine but had no effect on responses from NMDA receptors containing the GluN2A or GluN2B subunits AMPA, kainate, and GABA or glycine receptors or a variety of other potential targets. These compounds represent a potent class of small molecule subunit-selective potentiators of NMDA receptors.