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Potential of Nociceptin/Orphanin FQ Peptide Analogs for Drug Development.

Authors :
Wtorek K
Janecka A
Source :
Chemistry & biodiversity [Chem Biodivers] 2021 Jan; Vol. 18 (1), pp. e2000871. Date of Electronic Publication: 2020 Dec 22.
Publication Year :
2021

Abstract

Nociceptin receptor (NOP) belongs to the family of opioid receptors but was discovered and characterized much later than the so called classical opioid receptors, μ, δ and κ (or MOP, DOP and KOP, resp.). Nociceptin/orphanin FQ (N/OFQ) is the endogenous ligand of this receptor and it controls numerous important functions in the central nervous system and in the periphery, so its analogs may be developed as innovative drugs for the treatment of a variety of conditions and pathological states. Availability of potent and selective ligands with high affinity to NOP receptor is essential to fully understand the role of NOP-N/OFQ system in the body, which in turn may lead to designing novel therapeutics. Here, we have focused on reviewing the structure of potent peptide-based agonists, antagonists, biased analogs and bivalent ligands that target NOP receptor.<br /> (© 2020 Wiley-VHCA AG, Zurich, Switzerland.)

Details

Language :
English
ISSN :
1612-1880
Volume :
18
Issue :
1
Database :
MEDLINE
Journal :
Chemistry & biodiversity
Publication Type :
Academic Journal
Accession number :
33351271
Full Text :
https://doi.org/10.1002/cbdv.202000871