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Structure-Based Design of Potent and Selective Ligands at the Four Adenosine Receptors

Structure-Based Design of Potent and Selective Ligands at the Four Adenosine Receptors

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f115c7958c5a494a9a1eab7fe8bc2ac6

Structure-Based Design of Potent and Selective Ligands at the Four Adenosine Receptors

About this item

Full title

Structure-Based Design of Potent and Selective Ligands at the Four Adenosine Receptors

Publisher

Switzerland: MDPI AG

Journal title

Molecules (Basel, Switzerland), 2017-11, Vol.22 (11), p.1945

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

The four receptors that signal for adenosine, A1, A2A, A2B and A3 ARs, belong to the superfamily of G protein-coupled receptors (GPCRs). They mediate a number of (patho)physiological functions and have attracted the interest of the biopharmaceutical sector for decades as potential drug targets. The many crystal structures of the A2A, and lately the...

Alternative Titles

Full title

Structure-Based Design of Potent and Selective Ligands at the Four Adenosine Receptors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_f115c7958c5a494a9a1eab7fe8bc2ac6

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f115c7958c5a494a9a1eab7fe8bc2ac6

Other Identifiers

ISSN

1420-3049,1431-5157

E-ISSN

1420-3049

DOI

10.3390/molecules22111945

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