Synthesis and Dopamine Receptor Modulating Activity of Novel Peptidomimetics of l-Prolyl-l-leucyl-glycinamide Featuring α,α-Disubstituted Amino Acids
In the present study, l-prolyl-l-leucyl-glycinamide (1) peptidomimetics 3a − 3d and 4a − 4d were synthesized utilizing α,α-disubstituted amino acids. These analogues were designed to explore the conformational effects of constraints at the φ3 and ψ3 torsion angles. Constrained conformations were ver...
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Veröffentlicht in: | Journal of medicinal chemistry 1999-04, Vol.42 (8), p.1441-1447 |
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Format: | Artikel |
Sprache: | eng |
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