A novel cyclic enkephalin analogue with potent opioid antagonist activity
The synthesis and in vitro activity profile of a potent opioid peptide antagonist lacking an N-terminal amino group are described. 2′,6′- Dimethyl substitution of the Tyr1 residue in opioid agonist peptides and deletion of the N-terminal amino
Weltrowska, Grazyna,Lu, Yixin,Lemieux, Carole,Chung, Nga N.,Schiller, Peter W.
p. 4731 - 4733
(2007/10/03)
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