A systematic review on the kappa opioid receptor and its ligands: New directions for the treatment of pain, anxiety, depression, and drug abuse

MIH Khan, BJ Sawyer, NS Akins, HV Le - European Journal of Medicinal …, 2022 - Elsevier
Kappa opioid receptor (KOR) is a member of the opioid receptor system, the G protein-
coupled receptors that are expressed throughout the peripheral and central nervous …

Natural products for the treatment of pain: chemistry and pharmacology of salvinorin A, mitragynine, and collybolide

S Chakraborty, S Majumdar - Biochemistry, 2020 - ACS Publications
Pain remains a very pervasive problem throughout medicine. Classical pain management is
achieved through the use of opiates belonging to the mu opioid receptor (MOR) class, which …

The G protein–biased κ-opioid receptor agonist RB-64 is analgesic with a unique spectrum of activities in vivo

KL White, JE Robinson, H Zhu, JF DiBerto… - … of Pharmacology and …, 2015 - ASPET
The hypothesis that functionally selective G protein–coupled receptor (GPCR) agonists may
have enhanced therapeutic benefits has revitalized interest for many GPCR targets. In …

Identification of novel functionally selective κ-opioid receptor scaffolds

KL White, AP Scopton, ML Rives, RV Bikbulatov… - Molecular …, 2014 - ASPET
The κ-opioid receptor (KOR)-dynorphin system has been implicated in the control of affect,
cognition, and motivation, and is thought to be dysregulated in mood and psychotic …

Synthesis and κ-opioid receptor activity of furan-substituted salvinorin A analogues

AP Riley, CE Groer, D Young, AW Ewald… - Journal of medicinal …, 2014 - ACS Publications
The neoclerodane diterpene salvinorin A, found in the leaves of Salvia divinorum, is a potent
κ-opioid receptor agonist, making it an attractive scaffold for development into a treatment for …

[HTML][HTML] From plant to chemistry: Sources of active opioid antinociceptive principles for medicinal chemistry and drug design

R Turnaturi, S Piana, S Spoto, G Costanzo, L Reina… - Molecules, 2023 - mdpi.com
Pain continues to be an enormous global health challenge, with millions of new untreated or
inadequately treated patients reported annually. With respect to current clinical applications …

Analgesic opioid ligand discovery based on nonmorphinan scaffolds derived from natural sources

MT Smith, D Kong, A Kuo, MZ Imam… - Journal of Medicinal …, 2022 - ACS Publications
Strong opioid analgesics, including morphine, are the mainstays for treating moderate to
severe acute pain and alleviating chronic cancer pain. However, opioid-related adverse …

A review of salvinorin analogs and their kappa-opioid receptor activity

JJ Roach, RA Shenvi - Bioorganic & medicinal chemistry letters, 2018 - Elsevier
The plant metabolite salvinorin A potently and selectively agonizes the human kappa-opioid
receptor, an emerging target for next-generation analgesics. Here we review analogs of the …

Salvinorin A analogs and other kappa-opioid receptor compounds as treatments for cocaine abuse

BM Kivell, AWM Ewald, TE Prisinzano - Advances in pharmacology, 2014 - Elsevier
Acute activation of kappa-opioid receptors produces anti-addictive effects by regulating
dopamine levels in the brain. Unfortunately, classic kappa-opioid agonists have undesired …

[图书][B] Kratom and other mitragynines: the chemistry and pharmacology of opioids from a non-opium source

RB Raffa - 2014 - books.google.com
Opioids such as morphine, codeine, and oxycodone are extracts or analogs isolated from a
single source: the opium poppy. For a long time, it was believed to be nature's only source of …