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- W2510273208 abstract "Recently, the tryptophan-containing noncationizable opioid peptides emerged with atypical structure and unexpected in vivo activity. Herein, we describe analogs of the naturally occurring mixed κ/μ-ligand c[Phe-d-Pro-Phe-Trp] 1 (CJ-15,208). Receptor affinity, selectivity, and agonism/antagonism varied upon enlarging macrocycle size, giving the μ-agonist 9 or the δ-antagonist 10 characterized by low nanomolar affinity. In particular, the μ-agonist c[β-Ala-d-Pro-Phe-Trp] 9 was shown to elicit potent antinociception in a mouse model of visceral pain upon systemic administration." @default.
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- W2510273208 date "2016-09-22" @default.
- W2510273208 modified "2023-09-28" @default.
- W2510273208 title "Versatile Picklocks To Access All Opioid Receptors: Tuning the Selectivity and Functional Profile of the Cyclotetrapeptide c[Phe-<scp>d</scp>-Pro-Phe-Trp] (CJ-15,208)" @default.
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- W2510273208 doi "https://doi.org/10.1021/acs.jmedchem.6b00420" @default.
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