Journal article
Dopamine receptor modulation by Pro-Leu-Gly-NH2 analogues possessing cyclic amino acid residues at the C-terminal position.
Abstract
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-3,4-dehydroprolinamide, L-azetidine-2-carboxamide, L-piperidine-2-carboxamide, and L-thiazolidine-4-carboxamide to give PLG analogues 2-10, respectively. The ability of these analogues to …
Authors
Johnson RL; Rajakumar G; Mishra RK
Journal
Journal of Medicinal Chemistry, Vol. 29, No. 10, pp. 2100–2104
Publisher
American Chemical Society (ACS)
Publication Date
October 1986
DOI
10.1021/jm00160a051
ISSN
0022-2623