Abstract
Two series of conformationally constrained analogues of Pro-Leu-Gly-NH2 (PLG) have been synthesized. In one series of analogues, the Leu-Gly-NH2 dipeptide segment of PLG was replaced with the γ-lactam residues 3(S)-and 3(R)-amino-2-oxopyrrolidineacetamide and the γ-lactam residue 3(S)-amino-2-oxopiperidineacetamide. The corresponding γ-lactam analogues of
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CITATION STYLE
APA
Yu, K. L., Johnson, R. L., Rajakumar, G., Srivastava, L. K., & Mishra, R. K. (1988). Dopamine Receptor Modulation by Conformationally ConstrainedAnalogues of Pro-Leu-Gly-NH2. Journal of Medicinal Chemistry, 31(7), 1430–1436. https://doi.org/10.1021/jm00402a031
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