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Multifunctional Enkephalin Analogs with a New Biological Profile: MOR/DOR Agonism and KOR Antagonism.
Lee, Yeon Sun; Remesic, Michael; Ramos-Colon, Cyf; Wu, Zhijun; LaVigne, Justin; Molnar, Gabriella; Tymecka, Dagmara; Misicka, Aleksandra; Streicher, John M; Hruby, Victor J; Porreca, Frank.
Afiliación
  • Lee YS; Department of Pharmacology, University of Arizona, Tucson, AZ 85724, USA.
  • Remesic M; Department of Chemistry and Biochemistry, University of Arizona, Tucson, AZ 85721, USA.
  • Ramos-Colon C; Department of Chemistry and Biochemistry, University of Arizona, Tucson, AZ 85721, USA.
  • Wu Z; ABC Resource, Plainsboro, NJ 08536, USA.
  • LaVigne J; Department of Pharmacology, University of Arizona, Tucson, AZ 85724, USA.
  • Molnar G; Department of Pharmacology, University of Arizona, Tucson, AZ 85724, USA.
  • Tymecka D; Faculty of Chemistry, University of Warsaw, Pasteura, PL-02-093 Warsaw, Poland.
  • Misicka A; Faculty of Chemistry, University of Warsaw, Pasteura, PL-02-093 Warsaw, Poland.
  • Streicher JM; Department of Pharmacology, University of Arizona, Tucson, AZ 85724, USA.
  • Hruby VJ; Department of Chemistry and Biochemistry, University of Arizona, Tucson, AZ 85721, USA.
  • Porreca F; Department of Pharmacology, University of Arizona, Tucson, AZ 85724, USA.
Biomedicines ; 9(6)2021 May 31.
Article en En | MEDLINE | ID: mdl-34072734
ABSTRACT
In our previous studies, we developed a series of mixed MOR/DOR agonists that are enkephalin-like tetrapeptide analogs with an N-phenyl-N-piperidin-4-ylpropionamide (Ppp) moiety at the C-terminus. Further SAR study on the analogs, initiated by the findings from off-target screening, resulted in the discovery of LYS744 (6, Dmt-DNle-Gly-Phe(p-Cl)-Ppp), a multifunctional ligand with MOR/DOR agonist and KOR antagonist activity (GTPγS assay IC50 = 52 nM, Imax = 122% cf. IC50 = 59 nM, Imax = 100% for naloxone) with nanomolar range of binding affinity (Ki = 1.3 nM cf. Ki = 2.4 nM for salvinorin A). Based on its unique biological profile, 6 is considered to possess high therapeutic potential for the treatment of chronic pain by modulating pathological KOR activation while retaining analgesic efficacy attributed to its MOR/DOR agonist activity.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Biomedicines Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Biomedicines Año: 2021 Tipo del documento: Article