Development and Application of Subtype-Selective Fluorescent Antagonists for the Study of the Human Adenosine A


Journal

Journal of medicinal chemistry
ISSN: 1520-4804
Titre abrégé: J Med Chem
Pays: United States
ID NLM: 9716531

Informations de publication

Date de publication:
27 05 2021
Historique:
pubmed: 17 3 2021
medline: 22 6 2021
entrez: 16 3 2021
Statut: ppublish

Résumé

The adenosine A

Identifiants

pubmed: 33724031
doi: 10.1021/acs.jmedchem.0c02067
doi:

Substances chimiques

Adenosine A1 Receptor Antagonists 0
Bridged Bicyclo Compounds 0
Fluorescent Dyes 0
Ligands 0
Octanes 0
Receptor, Adenosine A1 0
bicyclo(2.2.2)octane 0
Xanthine 1AVZ07U9S7

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

6670-6695

Subventions

Organisme : Medical Research Council
ID : MR/N020081/1
Pays : United Kingdom

Auteurs

Eleonora Comeo (E)

Medicinal Chemistry, Monash University, Parkville, Victoria 3052, Australia.
Division of Biomolecular Sciences and Medicinal Chemistry, School of Pharmacy, Biodiscovery Institute, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
Centre of Membrane Proteins and Receptors (COMPARE), University of Birmingham, B15 2TT and University of Nottingham, Birmingham NG7 2UH, United Kingdom.

Phuc Trinh (P)

Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria 3052, Australia.

Anh T Nguyen (AT)

Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria 3052, Australia.

Cameron J Nowell (CJ)

Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria 3052, Australia.

Nicholas D Kindon (ND)

Division of Biomolecular Sciences and Medicinal Chemistry, School of Pharmacy, Biodiscovery Institute, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
Centre of Membrane Proteins and Receptors (COMPARE), University of Birmingham, B15 2TT and University of Nottingham, Birmingham NG7 2UH, United Kingdom.

Mark Soave (M)

Division of Physiology, Pharmacology and Neuroscience, School of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham NG7 2UH, United Kingdom.
Centre of Membrane Proteins and Receptors (COMPARE), University of Birmingham, B15 2TT and University of Nottingham, Birmingham NG7 2UH, United Kingdom.

Leigh A Stoddart (LA)

Division of Physiology, Pharmacology and Neuroscience, School of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham NG7 2UH, United Kingdom.
Centre of Membrane Proteins and Receptors (COMPARE), University of Birmingham, B15 2TT and University of Nottingham, Birmingham NG7 2UH, United Kingdom.

Jonathan M White (JM)

School of Chemistry and the Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Victoria 3010, Australia.

Stephen J Hill (SJ)

Division of Physiology, Pharmacology and Neuroscience, School of Life Sciences, Queens Medical Centre, University of Nottingham, Nottingham NG7 2UH, United Kingdom.
Centre of Membrane Proteins and Receptors (COMPARE), University of Birmingham, B15 2TT and University of Nottingham, Birmingham NG7 2UH, United Kingdom.

Barrie Kellam (B)

Division of Biomolecular Sciences and Medicinal Chemistry, School of Pharmacy, Biodiscovery Institute, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
Centre of Membrane Proteins and Receptors (COMPARE), University of Birmingham, B15 2TT and University of Nottingham, Birmingham NG7 2UH, United Kingdom.

Michelle L Halls (ML)

Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria 3052, Australia.

Lauren T May (LT)

Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria 3052, Australia.

Peter J Scammells (PJ)

Medicinal Chemistry, Monash University, Parkville, Victoria 3052, Australia.

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Classifications MeSH