D Lodge

Quinoxalinediones: potent competitive non-NMDA glutamate receptor antagonists.

S N Davies, E. J. Fletcher, E J Fletcher, 1988, Science.

3-Phenyl-4-hydroxyquinolin-2(1H)-ones: potent and selective antagonists at the strychnine-insensitive glycine site on the N-methyl-D-aspartate receptor complex.

D. Lodge, E. Pralong, J. Wikel, 1992, Journal of medicinal chemistry.

A novel, competitive mGlu(5) receptor antagonist (LY344545) blocks DHPG-induced potentiation of NMDA responses but not the induction of LTP in rat hippocampal slices.

D D Schoepp, Z A Bortolotto, G L Collingridge, 2000, British journal of pharmacology.

Noncompetitive excitatory amino acid receptor antagonists.

D. Lodge, K. Johnson, K M Johnson, 1990, Trends in pharmacological sciences.

Pharmacological characterization of LY233053: a structurally novel tetrazole-substituted competitive N-methyl-D-aspartic acid antagonist with a short duration of action.

P. Ornstein, D. Schoepp, D. Lodge, 1990, The Journal of pharmacology and experimental therapeutics.

6-substituted decahydroisoquinoline-3-carboxylic acids as potent and selective conformationally constrained NMDA receptor antagonists.

P. Ornstein, D. Schoepp, D. Lodge, 1992, Journal of medicinal chemistry.