Nociceptin/orphanin FQ receptor structure, signaling, ligands, functions, and interactions with opioid systems
L Toll, MR Bruchas, BM Cox, NT Zaveri - Pharmacological reviews, 2016 - ASPET
The NOP receptor (nociceptin/orphanin FQ opioid peptide receptor) is the most recently
discovered member of the opioid receptor family and, together with its endogenous ligand …
discovered member of the opioid receptor family and, together with its endogenous ligand …
Oxycodone in the opioid epidemic: high 'liking','wanting', and abuse liability
It is estimated that nearly a third of people who abuse drugs started with prescription opioid
medicines. Approximately, 11.5 million Americans used prescription drugs recreationally in …
medicines. Approximately, 11.5 million Americans used prescription drugs recreationally in …
Targeting multiple opioid receptors–improved analgesics with reduced side effects?
T Günther, P Dasgupta, A Mann, E Miess… - British journal of …, 2018 - Wiley Online Library
Classical opioid analgesics, including morphine, mediate all of their desired and undesired
effects by specific activation of the μ‐opioid receptor (μ receptor). The use of morphine for …
effects by specific activation of the μ‐opioid receptor (μ receptor). The use of morphine for …
[HTML][HTML] Hot topics in opioid pharmacology: mixed and biased opioids
AAH Azzam, J McDonald, DG Lambert - British journal of anaesthesia, 2019 - Elsevier
Analgesic design and evaluation have been driven by the desire to create high-affinity high-
selectivity mu (μ)-opioid peptide (MOP) receptor agonists. Such ligands are the mainstay of …
selectivity mu (μ)-opioid peptide (MOP) receptor agonists. Such ligands are the mainstay of …
Strategies towards safer opioid analgesics—A review of old and upcoming targets
BR Varga, JM Streicher… - British journal of …, 2023 - Wiley Online Library
Opioids continue to be of use for the treatment of pain. Most clinically used analgesics target
the μ opioid receptor whose activation results in adverse effects like respiratory depression …
the μ opioid receptor whose activation results in adverse effects like respiratory depression …
Cebranopadol: a novel potent analgesic nociceptin/orphanin FQ peptide and opioid receptor agonist
K Linz, T Christoph, TM Tzschentke, T Koch… - … of Pharmacology and …, 2014 - ASPET
Cebranopadol (trans-6′-fluoro-4′, 9′-dihydro-N, N-dimethyl-4-phenyl-spiro [cyclohexane-
1, 1′(3′ H)-pyrano [3, 4-b] indol]-4-amine) is a novel analgesic nociceptin/orphanin FQ …
1, 1′(3′ H)-pyrano [3, 4-b] indol]-4-amine) is a novel analgesic nociceptin/orphanin FQ …
Respiratory depressant effects of fentanyl analogs are opioid receptor-mediated
Opioid-related fatalities involving synthetic opioids have reached unprecedented levels. This
study evaluated the respiratory depressant effects of seven fentanyl analogs that have either …
study evaluated the respiratory depressant effects of seven fentanyl analogs that have either …
A bifunctional nociceptin and mu opioid receptor agonist is analgesic without opioid side effects in nonhuman primates
Misuse of prescription opioids, opioid addiction, and overdose underscore the urgent need
for developing addiction-free effective medications for treating severe pain. Mu opioid …
for developing addiction-free effective medications for treating severe pain. Mu opioid …
Mortality risk of opioid substitution therapy with methadone versus buprenorphine: a retrospective cohort study
Background Opioid dependence increases risk of premature mortality. Opioid substitution
therapy with methadone or buprenorphine reduces mortality risk, especially for drug-related …
therapy with methadone or buprenorphine reduces mortality risk, especially for drug-related …
Morphine alkaloids: History, biology, and synthesis
C Wicks, T Hudlicky, U Rinner - The Alkaloids: Chemistry and Biology, 2021 - Elsevier
This chapter provides a short overview of the history of morphine since it's isolation by
Sertürner in 1805. The biosynthesis of the title alkaloid as well as all total and formal …
Sertürner in 1805. The biosynthesis of the title alkaloid as well as all total and formal …