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FEBS Lett ; 351(3): 308-10, 1994 Sep 12.
Article in English | MEDLINE | ID: mdl-7915993

ABSTRACT

Four new [D-MetO2]dermorphin tetrapeptides with substituted N- and C-terminal groups and a thymine-modified alanine residue at position 4 were prepared and tested for their activity. All analogues were found to be mu-opioid receptor ligands. Two of them, H-Tyr-D-MetO-Phe-TalNHR (R = H, Ad) displayed an extremely high mu-opioid receptor selectivity comparable with that of the most mu-selective agonists among opioid peptides.


Subject(s)
Alanine/metabolism , Analgesics, Opioid/metabolism , Oligopeptides/metabolism , Receptors, Opioid, mu/metabolism , Thymine/metabolism , Amino Acid Sequence , Analgesics, Opioid/chemistry , Analgesics, Opioid/pharmacology , Animals , Brain/drug effects , Brain/metabolism , Guinea Pigs , Ileum/drug effects , Ileum/metabolism , In Vitro Techniques , Male , Mice , Molecular Sequence Data , Oligopeptides/chemistry , Oligopeptides/pharmacology , Opioid Peptides , Rats , Receptors, Opioid, mu/drug effects , Vas Deferens/drug effects , Vas Deferens/metabolism
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