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Design, synthesis and pharmacological characterization of endomorphin analogues with non-cyclic amino acid residues in position 24386
Publication Type: Peer reviewed scientific article Authors: Perlikowska,R.; Fichna,J.; Wyrebska,A.; J Poels; J. Vanden Broeck; Toth,G.; Storr,M.; J.C. do Rego; A.E. Janecka Source: Basic ...
Novel highly potent mu-opioid receptor antagonist based on endomorphin-2 structure4392
Publication Type: Peer reviewed scientific article Authors: Fichna,J.; do-Rego,J.C.; Janecki,T.; Staniszewska,R.; J Poels; J. Vanden Broeck; Costentin,J.; Schiller,P.W.; A.E. Janecka Source: ...
Synthesis and characterization of potent and selective mu-opioid receptor antagonists, [Dmt(1), D-2-Nal(4)]endomorphin-1 (Antanal-1) and [Dmt(1), D-2-Nal(4)]endomorphin-2 (Antanal-2)4395
Publication Type: Peer reviewed scientific article Authors: Fichna,J.; do-Rego,J.C.; Chung,N.N.; Lemieux,C.; Schiller,P.W.; J Poels; J. Vanden Broeck; Costentin,J.; A.E. Janecka Source: J.Med.Chem., ...