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Therapeutic application of GPR119 ligands in metabolic disorders

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dc.contributor.authorYang, Jin Won-
dc.contributor.authorKim, Hyo Seon-
dc.contributor.authorChoi, Yong-Won-
dc.contributor.authorKim, Young-Mi-
dc.contributor.authorKang, Keon Wook-
dc.date.accessioned2021-06-22T12:21:51Z-
dc.date.available2021-06-22T12:21:51Z-
dc.date.created2021-01-21-
dc.date.issued2018-02-
dc.identifier.issn1462-8902-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/6815-
dc.description.abstractGPR119 belongs to the G protein-coupled receptor family and exhibits dual modes of action upon ligand-dependent activation: pancreatic secretion of insulin in a glucose-dependent manner and intestinal secretion of incretins. Hence, GPR119 has emerged as a promising target for treating type 2 diabetes mellitus without causing hypoglycaemia. However, despite continuous efforts by many major pharmaceutical companies, no synthetic GPR119 ligand has been approved as a new class of anti-diabetic agents thus far, nor has any passed beyond phase II clinical studies. Herein, we summarize recent advances in research concerning the physiological/pharmacological effects of GPR119 and its synthetic ligands on the regulation of energy metabolism, and we speculate on future applications of GPR119 ligands for the treatment of metabolic diseases, focusing on non-alcoholic fatty liver disease.-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-
dc.titleTherapeutic application of GPR119 ligands in metabolic disorders-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Young-Mi-
dc.identifier.doi10.1111/dom.13062-
dc.identifier.scopusid2-s2.0-85040733725-
dc.identifier.wosid000422678600004-
dc.identifier.bibliographicCitationDIABETES OBESITY & METABOLISM, v.20, no.2, pp.257 - 269-
dc.relation.isPartOfDIABETES OBESITY & METABOLISM-
dc.citation.titleDIABETES OBESITY & METABOLISM-
dc.citation.volume20-
dc.citation.number2-
dc.citation.startPage257-
dc.citation.endPage269-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEndocrinology & Metabolism-
dc.relation.journalWebOfScienceCategoryEndocrinology & Metabolism-
dc.subject.keywordPlusFATTY LIVER-DISEASE-
dc.subject.keywordPlusPROTEIN-COUPLED RECEPTOR-
dc.subject.keywordPlusGLUCAGON-LIKE PEPTIDE-1-
dc.subject.keywordPlusTYPE-2 DIABETES-MELLITUS-
dc.subject.keywordPlusINSULIN-SECRETION-
dc.subject.keywordPlusNONALCOHOLIC STEATOHEPATITIS-
dc.subject.keywordPlusWEIGHT-LOSS-
dc.subject.keywordPlusPHARMACOLOGICAL MANAGEMENT-
dc.subject.keywordPlusGLYCEMIC CONTROL-
dc.subject.keywordPlusPANCREATIC BETA-
dc.subject.keywordAuthorGPR119-
dc.subject.keywordAuthormetabolic diseases-
dc.subject.keywordAuthornon-alcoholic fatty liver disease-
dc.subject.keywordAuthorphysiological-
dc.subject.keywordAuthorpharmacological effects-
dc.subject.keywordAuthorsynthetic ligands-
dc.subject.keywordAuthortype 2 diabetes mellitus-
dc.identifier.urlhttps://dom-pubs.onlinelibrary.wiley.com/doi/10.1111/dom.13062-
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