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N-methylthioureas as new agonists of retinoic acid receptor-related orphan receptor

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dc.contributor.authorPark, Yohan-
dc.contributor.authorHong, Suckchang-
dc.contributor.authorLee, Myungmo-
dc.contributor.authorJung, Hyojun-
dc.contributor.authorCho, Won-Jea-
dc.contributor.authorKim, Eun-Jin-
dc.contributor.authorSon, Ho-Young-
dc.contributor.authorLee, Mi-Ock-
dc.contributor.authorPark, Hyeung-geun-
dc.date.accessioned2024-05-14T07:18:44Z-
dc.date.available2024-05-14T07:18:44Z-
dc.date.created2017-11-15-
dc.date.issued2012-08-
dc.identifier.citationArchives of Pharmacal Research, Vol.35 No.8, pp.1393-1401-
dc.identifier.issn0253-6269-
dc.identifier.urihttps://hdl.handle.net/10371/202029-
dc.description.abstractThirty two thiourea derivatives were prepared and their agonistic activities on the retinoic acid receptor-related orphan receptor alpha (ROR alpha) were evaluated. The replacement of the 3-allyl-2-imino-thiazolidin-4-one moiety of the lead compound CGP52608 (1) with various functional group substituted aromatic rings, improved the agonistic activity of ROR alpha. Among the prepared derivatives, 1-methyl-3-(4-phenoxy-benzyl)-thiourea (32) showed 2.6-fold higher agonistic activity than CGP52608 in the ROR alpha-activation assay.-
dc.language영어-
dc.publisher대한약학회-
dc.titleN-methylthioureas as new agonists of retinoic acid receptor-related orphan receptor-
dc.typeArticle-
dc.identifier.doi10.1007/s12272-012-0809-0-
dc.citation.journaltitleArchives of Pharmacal Research-
dc.identifier.wosid000308244800010-
dc.identifier.scopusid2-s2.0-84868096066-
dc.citation.endpage1401-
dc.citation.number8-
dc.citation.startpage1393-
dc.citation.volume35-
dc.identifier.kciidART001686333-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorHong, Suckchang-
dc.contributor.affiliatedAuthorLee, Mi-Ock-
dc.contributor.affiliatedAuthorPark, Hyeung-geun-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusROR-GAMMA-T-
dc.subject.keywordPlusNUCLEAR RECEPTOR-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusTRANSCRIPTIONAL ACTIVATION-
dc.subject.keywordPlusALPHA-
dc.subject.keywordPlusLIGAND-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusCHOLESTEROL-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusSUBFAMILY-
dc.subject.keywordAuthorThiourea derivatives-
dc.subject.keywordAuthorAgonists-
dc.subject.keywordAuthorRetinoid acid receptor-related orphan receptor alpha-
dc.subject.keywordAuthorCGP52608-
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  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Development of methodologies using metal catalyst, Total synthesis of natural products

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