Dopamine Receptor Modulation by Pro-Leu-Gly-NH2 Analogues Possessing Cyclic Amino Acid Residues at the C-Terminal Position

Article abstract of DOI:10.1021/jm00160a051

The synthesis of several analogues of L-prolyl-L-leucylglycinamide (PLG) was carried out in which the glycinamide residue was replaced with the following cyclic amino acid residues: L- and D-prolinamide, (+)- and (-)-thiazolidine-2-carboxamide, L- and D-3