Format

Send to

Choose Destination
See comment in PubMed Commons below
Trends Pharmacol Sci. 2014 Jul;35(7):308-16. doi: 10.1016/j.tips.2014.04.007. Epub 2014 May 28.

Biased ligands at G-protein-coupled receptors: promise and progress.

Author information

1
Trevena Inc., 1018 West 8th Avenue, Suite A, King of Prussia, PA 19406, USA. Electronic address: jviolin@trevenainc.com.
2
Trevena Inc., 1018 West 8th Avenue, Suite A, King of Prussia, PA 19406, USA.

Erratum in

  • Trends Pharmacol Sci. 2014 Sep;35(9):489.

Abstract

Drug discovery targeting G protein-coupled receptors (GPCRs) is no longer limited to seeking agonists or antagonists to stimulate or block cellular responses associated with a particular receptor. GPCRs are now known to support a diversity of pharmacological profiles, a concept broadly referred to as functional selectivity. In particular, the concept of ligand bias, whereby a ligand stabilizes subsets of receptor conformations to engender novel pharmacological profiles, has recently gained increasing prominence. This review discusses how biased ligands may deliver safer, better tolerated, and more efficacious drugs, and highlights several biased ligands that are in clinical development. Biased ligands targeting the angiotensin II type 1 receptor and the μ opioid receptor illustrate the translation of the biased ligand concept from basic biology to clinical drug development.

KEYWORDS:

TRV027; TRV130; angiotensin; functional selectivity; opioid; β-arrestin

PMID:
24878326
DOI:
10.1016/j.tips.2014.04.007
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Elsevier Science
    Loading ...
    Support Center