New paradigms in purinergic receptor ligand discovery.


Journal

Neuropharmacology
ISSN: 1873-7064
Titre abrégé: Neuropharmacology
Pays: England
ID NLM: 0236217

Informations de publication

Date de publication:
01 06 2023
Historique:
received: 05 01 2023
revised: 28 02 2023
accepted: 11 03 2023
pmc-release: 01 06 2024
medline: 28 3 2023
pubmed: 16 3 2023
entrez: 15 3 2023
Statut: ppublish

Résumé

The discovery and clinical implementation of modulators of adenosine, P2Y and P2X receptors (comprising nineteen subtypes) have progressed dramatically in ∼50 years since Burnstock's definition of purinergic signaling. Although most clinical trials of selective ligands (agonists and antagonists) of certain purinergic receptors failed, there is a renewed impetus to redirect efforts to new disease conditions and the discovery of more selective or targeted compounds with potentially reduced side effects, such as biased GPCR agonists. The elucidation of new receptor and enzyme structures is steering rational design of potent and selective agonists, antagonists, allosteric modulators and inhibitors. A

Identifiants

pubmed: 36921890
pii: S0028-3908(23)00093-X
doi: 10.1016/j.neuropharm.2023.109503
pmc: PMC10233512
mid: NIHMS1884019
pii:
doi:

Substances chimiques

Ligands 0
Receptors, Purinergic 0
Adenosine K72T3FS567
Purinergic P1 Receptor Antagonists 0

Types de publication

Journal Article Review Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

109503

Subventions

Organisme : Intramural NIH HHS
ID : Z01 DK031116
Pays : United States
Organisme : Intramural NIH HHS
ID : Z01 DK031117
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIA DK031116
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIA DK031117
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors (KAJ, BP, ZW, and AP) declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Kenneth A Jacobson (KA)

Molecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD, 20892, USA. Electronic address: kennethJ@niddk.nih.gov.

Balaram Pradhan (B)

Molecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD, 20892, USA. Electronic address: balaram.pradhan@nih.gov.

Zhiwei Wen (Z)

Molecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD, 20892, USA. Electronic address: zhiwei.wen@nih.gov.

Asmita Pramanik (A)

Molecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD, 20892, USA. Electronic address: asmita.pramanik@nih.gov.

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Classifications MeSH