Cebranopadol: A Novel First-in-Class Potent Analgesic Acting via NOP and Opioid Receptors.
Cancer pain
Chronic low back pain
Diabetic peripheral neuropathy
Nociceptin/orphanin FQ
Postoperative pain
Respiratory depression
Journal
Handbook of experimental pharmacology
ISSN: 0171-2004
Titre abrégé: Handb Exp Pharmacol
Pays: Germany
ID NLM: 7902231
Informations de publication
Date de publication:
2019
2019
Historique:
pubmed:
31
3
2019
medline:
28
7
2019
entrez:
31
3
2019
Statut:
ppublish
Résumé
Cebranopadol is a novel first-in-class analgesic with highly potent agonistic activity at nociceptin/orphanin FQ peptide (NOP) and opioid receptors. It is highly potent and efficacious across a broad range of preclinical pain models. Its side effect profile is better compared to typical opioids. Mechanistic studies have shown that cebranopadol's activity at NOP receptors contributes to its anti-hyperalgesic effects while ameliorating some of its opioid-type side effects, including respiratory depression and abuse potential. Phase II of clinical development has been completed, demonstrating efficacy and good tolerability in acute and chronic pain conditions.This article focusses on reviewing data on the preclinical in vitro and in vivo pharmacology, safety, and tolerability, as well as clinical trials with cebranopadol.
Identifiants
pubmed: 30927089
doi: 10.1007/164_2019_206
doi:
Substances chimiques
6'-fluoro-4',9'-dihydro-N,N-dimethyl-4-phenylspiro(cyclohexane-1,1'(3'H)-pyrano(3,4-b)indol)-4-amine
0
Analgesics, Opioid
0
Indoles
0
Opioid Peptides
0
Receptors, Opioid
0
Spiro Compounds
0
Types de publication
Journal Article
Langues
eng