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Dopamine receptor modulation by Pro-Leu-Gly-NH2...
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