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Recent updates on GPCR biased agonism

dc.contributor.authorPupo, Andre S. [UNESP]
dc.contributor.authorDuarte, Diego A.
dc.contributor.authorLima, Vanessa [UNESP]
dc.contributor.authorTeixeira, Larissa B.
dc.contributor.authorParreiras-e-Silva, Lucas T.
dc.contributor.authorCosta-Neto, Claudio M.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2018-11-26T17:06:44Z
dc.date.available2018-11-26T17:06:44Z
dc.date.issued2016-10-01
dc.description.abstractG protein-coupled receptors (GPCRs) are the most important targets for drug discovery and not surprisingly similar to 40% of all drugs currently in the market act on these receptors. Currently, one of the most active areas in GPCRs signaling is biased agonism, a phenomenon that occurs when a given ligand is able to preferentially activate one (or some) of the possible signaling pathways. In this review, we highlight the most recent findings about biased agonism, including an extension of this concept to intracellular signaling, allosterism, strategies for assessment and interpretation, and perspectives of therapeutic applications for biased agonists. (C) 2016 Elsevier Ltd. All rights reserved.en
dc.description.affiliationUNESP, Inst Biociencias, Dept Pharmacol, Botucatu, SP, Brazil
dc.description.affiliationUniv Sao Paulo, Dept Biochem & Immunol, Fac Med Ribeirao Preto, BR-14049900 Ribeirao Preto, SP, Brazil
dc.description.affiliationUnespUNESP, Inst Biociencias, Dept Pharmacol, Botucatu, SP, Brazil
dc.format.extent49-57
dc.identifierhttp://dx.doi.org/10.1016/j.phrs.2016.01.031
dc.identifier.citationPharmacological Research. London: Academic Press Ltd- Elsevier Science Ltd, v. 112, p. 49-57, 2016.
dc.identifier.doi10.1016/j.phrs.2016.01.031
dc.identifier.fileWOS000385595100005.pdf
dc.identifier.issn1043-6618
dc.identifier.urihttp://hdl.handle.net/11449/162068
dc.identifier.wosWOS:000385595100005
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofPharmacological Research
dc.relation.ispartofsjr1,811
dc.rights.accessRightsAcesso abertopt
dc.sourceWeb of Science
dc.subjectGPCR
dc.subject7TMR
dc.subjectFunctional selectivity
dc.titleRecent updates on GPCR biased agonismen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isOrgUnitOfPublicationab63624f-c491-4ac7-bd2c-767f17ac838d
relation.isOrgUnitOfPublication.latestForDiscoveryab63624f-c491-4ac7-bd2c-767f17ac838d
unesp.author.lattes2224433126054725[1]
unesp.author.orcid0000-0001-6627-3448[1]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentFarmacologia - IBBpt

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