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Discovery of Novel Delta Opioid Receptor (DOR) Inverse Agonist and Irreversible (Non-Competitive) Antagonists.
Tanguturi, Parthasaradhireddy; Pathak, Vibha; Zhang, Sixue; Moukha-Chafiq, Omar; Augelli-Szafran, Corinne E; Streicher, John M.
Affiliation
  • Tanguturi P; Department of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ 85724, USA.
  • Pathak V; Department of Chemistry, Division of Drug Discovery, Southern Research Institute, Birmingham, AL 35205, USA.
  • Zhang S; Department of Chemistry, Division of Drug Discovery, Southern Research Institute, Birmingham, AL 35205, USA.
  • Moukha-Chafiq O; Department of Chemistry, Division of Drug Discovery, Southern Research Institute, Birmingham, AL 35205, USA.
  • Augelli-Szafran CE; Department of Chemistry, Division of Drug Discovery, Southern Research Institute, Birmingham, AL 35205, USA.
  • Streicher JM; Department of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ 85724, USA.
Molecules ; 26(21)2021 11 05.
Article in En | MEDLINE | ID: mdl-34771099
ABSTRACT
The delta opioid receptor (DOR) is a crucial receptor system that regulates pain, mood, anxiety, and similar mental states. DOR agonists, such as SNC80, and DOR-neutral antagonists, such as naltrindole, were developed to investigate the DOR in vivo and as potential therapeutics for pain and depression. However, few inverse agonists and non-competitive/irreversible antagonists have been developed, and none are widely available. This leaves a gap in our pharmacological toolbox and limits our ability to investigate the biology of this receptor. Thus, we designed and synthesized the novel compounds SRI-9342 as an irreversible antagonist and SRI-45128 as an inverse agonist. These compounds were then evaluated in vitro for their binding affinity by radioligand binding, their functional activity by 35S-GTPγS coupling, and their cAMP accumulation in cells expressing the human DOR. Both compounds demonstrated high binding affinity and selectivity at the DOR, and both displayed their hypothesized molecular pharmacology of irreversible antagonism (SRI-9342) or inverse agonism (SRI-45128). Together, these results demonstrate that we have successfully designed new inverse agonists and irreversible antagonists of the DOR based on a novel chemical scaffold. These new compounds will provide new tools to investigate the biology of the DOR or even new potential therapeutics.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Binding, Competitive / Receptors, Opioid, delta / Drug Discovery / Analgesics, Opioid Limits: Humans Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Binding, Competitive / Receptors, Opioid, delta / Drug Discovery / Analgesics, Opioid Limits: Humans Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2021 Document type: Article Affiliation country: