Biased agonism: An emerging paradigm in GPCR drug discovery

Z Rankovic, TF Brust, LM Bohn - Bioorganic & medicinal chemistry letters, 2016 - Elsevier
G protein coupled receptors have historically been one of the most druggable classes of
cellular proteins. The members of this large receptor gene family couple to primary effectors …

Clerodane diterpenes: sources, structures, and biological activities

R Li, SL Morris-Natschke, KH Lee - Natural product reports, 2016 - pubs.rsc.org
Covering: 1990 to 2015 The clerodane diterpenoids are a widespread class of secondary
metabolites and have been found in several hundreds of plant species from various families …

Mitragynine/corynantheidine pseudoindoxyls as opioid analgesics with mu agonism and delta antagonism, which do not recruit β-arrestin-2

A Váradi, GF Marrone, TC Palmer… - Journal of medicinal …, 2016 - ACS Publications
Natural products found in Mitragyna speciosa, commonly known as kratom, represent
diverse scaffolds (indole, indolenine, and spiro pseudoindoxyl) with opioid activity, providing …

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 …

Neuropharmacology of the naturally occurring κ-opioid hallucinogen salvinorin A

CW Cunningham, RB Rothman, TE Prisinzano - Pharmacological reviews, 2011 - ASPET
Salvia divinorum is a perennial sage native to Oaxaca, Mexico, that has been used
traditionally in divination rituals and as a treatment for the “semimagical” disease panzón de …

Endogenous opiates and behavior: 2006

RJ Bodnar - Peptides, 2007 - Elsevier
This paper is the 29th consecutive installment of the annual review of research concerning
the endogenous opioid system, now spanning 30 years of research. It summarizes papers …

[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 as probes in opioid pharmacology

TE Prisinzano, RB Rothman - Chemical reviews, 2008 - ACS Publications
The opium poppy, PapaVer somniferum, is one of several plants that have profoundly
affected human history. 1 It has provided an unmatched medicine for the relief of pain for …