Molecular pharmacology of P2Y receptor subtypes.
Animals
Drug Delivery Systems
/ methods
Drug Design
Humans
Platelet Aggregation
/ drug effects
Purinergic P2Y Receptor Agonists
/ administration & dosage
Purinergic P2Y Receptor Antagonists
/ administration & dosage
Receptors, Purinergic P2Y
/ metabolism
Signal Transduction
/ drug effects
Vascular Diseases
/ drug therapy
Adenine nucleotides
Agonist
Antagonist
Crystal structure
P2Y receptors
Uracil nucleotides
Journal
Biochemical pharmacology
ISSN: 1873-2968
Titre abrégé: Biochem Pharmacol
Pays: England
ID NLM: 0101032
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
received:
19
10
2020
revised:
06
12
2020
accepted:
07
12
2020
pubmed:
15
12
2020
medline:
15
9
2021
entrez:
14
12
2020
Statut:
ppublish
Résumé
Professor Geoffrey Burnstock proposed the concept of purinergic signaling via P1 and P2 receptors. P2Y receptors are G-protein-coupled receptors (GPCRs) for extracellular adenine and uracil nucleotides. Eight mammalian P2Y receptor subtypes have been identified. They are divided into two subgroups (P2Y
Identifiants
pubmed: 33309519
pii: S0006-2952(20)30597-9
doi: 10.1016/j.bcp.2020.114361
pii:
doi:
Substances chimiques
Purinergic P2Y Receptor Agonists
0
Purinergic P2Y Receptor Antagonists
0
Receptors, Purinergic P2Y
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
114361Informations de copyright
Copyright © 2020. Published by Elsevier Inc.