Trifluoromethylthio and trifluoromethyl functionalization of endomorphin-1 enhances its hydrophobicity and plasma stability while preserving its affinity for the $\mu$-opioid receptor

Gregorc, Jure (avtor), De Neve, Jolien (avtor), Guitot, Karine (avtor), Holleran, Brian J. (avtor), Lensen, Nathalie (avtor), Gendron, Louis (avtor), Brigaud, Thierry (avtor), Iskra, Jernej (avtor), Ballet, Steven (avtor), Chaume, Grégory (avtor)

The incorporation of fluorinated amino acid residues into peptides represents a promising strategy for improving the pharmacokinetic properties of bioactive peptides. Herein, we report the solid-phase synthesis (SPPS) of a set of ten SCF$_{3^-}$ or CF$_{3^-}$ modified neuropeptide analogs based on endomorphin-1 (EM1). EM1, a selective subnanomolar μ-opioid receptor (μOR) agonist with poor metabolic stability (t$_{1/2}$ = 6 min in human plasma), was selected as a model to evaluate the effects of SCF$_3$ and CF$_3$ functionalization on the pharmacokinetic profile of short bioactive peptides. The syntheses of eight ready-to-use SCF$_{3^-}$ or CF$_{3^-}$ containing building blocks for SPPS and their incorporation into peptides are reported. In vitro μOR binding and functional activity assays demonstrated that most fluorinated analogs retained binding affinity and potency, accompanied by increased hydrophobicity. Among the series, modification of the pharmacophoric Tyr1 residue with l-Dmt(3-SCF$_3$) yielded the most favorable profile (K$_i$ = 1.4 nM, EC$_{50}$ = 0.9 nM). Plasma stability studies revealed a significant increase in half-life for this ligand (72-fold relative to EM1 and 14-fold relative to EM1(Dmt$^1$)), and thus, further demonstrated the potential of SCF$_{3^-}$containing amino acids in therapeutic peptide design.

• Jezik: Angleški jezik
• Ključne besede: ligands, peptides, opioid receptors, fluorine, metabolic stability
• Vrsta gradiva: Članek v reviji
• Tipologija: 1.01 - Izvirni znanstveni članek
• Organizacija: FKKT - Fakulteta za kemijo in kemijsko tehnologijo
• Status publikacije: Objavljeno
• Različica publikacije: Objavljena publikacija
• Leto izida: 2026
• Št. strani: Str. 5598-5607
• Številčenje: Vol. 91, iss. 16
• PID: 20.500.12556/RUL-182063
• UDK: 547.9:546.16
• ISSN pri članku: 0022-3263
• DOI: 10.1021/acs.joc.6c00321
• COBISS.SI-ID: 276208643
• Datum objave v RUL: 23.04.2026

Gradivo je del revije

• Naslov: Journal of organic chemistry
• Skrajšan naslov: J. org. chem.
• Založnik: American Chemical Society.
• ISSN: 0022-3263
• COBISS.SI-ID: 235287

Licence

• Licenca: CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
• Povezava: http://creativecommons.org/licenses/by/4.0/deed.sl
• Opis: To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

• Jezik: Slovenski jezik
• Ključne besede: ligandi, peptidi, opioidni receptorji, fluor, metabolna stabilnost