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Suppression of inducible nitric oxide synthase expression induced by Toll-like receptor agonists by (E)-1-(2-(2-nitrovinyl)phenyl)pyrrolidine

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dc.contributor.authorEom, Sang-Hoon-
dc.contributor.authorGu, Gyo-Jeong-
dc.contributor.authorSuh, Chang Won-
dc.contributor.authorKoh, Kwang Oh-
dc.contributor.authorKim, Dae Young-
dc.contributor.authorEom, Yong-Bin-
dc.contributor.authorYoun, Hyung-Sun-
dc.date.accessioned2021-08-12T00:45:48Z-
dc.date.available2021-08-12T00:45:48Z-
dc.date.issued2013-10-
dc.identifier.issn1567-5769-
dc.identifier.issn1878-1705-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/13331-
dc.description.abstractToll-like receptors (TLRs) recognize many pathogen-associated molecular patterns and induce innate immunity. TLR signaling pathways induce the activation of various transcription factors, such as nuclear factor-kappa B (NF-kappa B), leading to the induction of pro-inflammatory gene products, such as inducible nitric oxide synthase (iNOS). Here, we investigated the effect of an (E)-1-(2-(2-nitrovinyl)phenyl)pyrrolidine (NVPP), previously synthesized in our laboratory, on inflammation by modulating NF-kappa B activation and iNOS expression induced by TLR agonists in murine macrophages. NVPP suppressed NF-kappa B activation and iNOS expression induced by lipopolysaccharide (TLR4 agonist), polyriboinosinic polyribocytidylic acid (TLR3 agonist), and macrophage-activating lipopeptide 2 kDa (TLR2 and TLR6 agonist). All the results suggest that NVPP is suitable for development as a new anti-inflammatory drug. (C) 2013 Elsevier B.V. All rights reserved.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleSuppression of inducible nitric oxide synthase expression induced by Toll-like receptor agonists by (E)-1-(2-(2-nitrovinyl)phenyl)pyrrolidine-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.intimp.2013.06.006-
dc.identifier.scopusid2-s2.0-84881511052-
dc.identifier.wosid000325122200008-
dc.identifier.bibliographicCitationInternational Immunopharmacology, v.17, no.2, pp 205 - 209-
dc.citation.titleInternational Immunopharmacology-
dc.citation.volume17-
dc.citation.number2-
dc.citation.startPage205-
dc.citation.endPage209-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusINFLAMMATORY CELLS-
dc.subject.keywordPlusRECOGNITION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusTBK1-
dc.subject.keywordAuthorToll-like receptor-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorNuclear factor-kappa B-
dc.subject.keywordAuthorInducible nitric oxide synthase-
dc.subject.keywordAuthor(E)-1-(2-(2-nitrovinyl)phenyl)pyrrolidine-
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