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dc.contributor.authorLi, Hailan-
dc.contributor.authorKim, Jandi-
dc.contributor.authorHahn, Hoh-Gyu-
dc.contributor.authorYun, Jun-
dc.contributor.authorJeong, Hyo-Soon-
dc.contributor.authorYun, Hye-Young-
dc.contributor.authorBaek, Kwang Jin-
dc.contributor.authorKwon, Nyoun Soo-
dc.contributor.authorMin, Young Sil-
dc.contributor.authorPark, Kyoung-Chan-
dc.contributor.authorKim, Dong-Seok-
dc.date.accessioned2024-01-20T09:34:17Z-
dc.date.available2024-01-20T09:34:17Z-
dc.date.created2021-09-04-
dc.date.issued2014-06-
dc.identifier.issn1226-4512-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/126756-
dc.description.abstractThe purpose of this study is to characterize the effects of KHG26792 (3-(naphthalen-2-yl(propoxy) methyl)azetidine hydrochloride), a potential skin whitening agent, on melanin synthesis and identify the underlying mechanism of action. Our data showed that KHG26792 significantly reduced melanin synthesis in a dose-dependent manner. Additionally, KHG26792 downregulated microphthalmia-associated transcription factor (MITF) and tyrosinase, the rate-limiting enzyme in melanogenesis, although tyrosinase was not inhibited directly. KHG26792 activated extracellular signal-regulated kinase (ERK), whereas an ERK pathway inhibitor, PD98059, rescued KHG26792-induced hypopigmentation. These results suggest that KHG26792 decreases melanin production via ERK activation. Moreover, the hypopiginentary effects of KHG26792 were confirmed in a pigmented skin equivalent model using Cervi comas Colla (deer antler glue), in which the color of the pigmented artificial skin became lighter after treatment with KHG26792. In summary, our findings suggest that KHG26792 is a novel skin whitening agent.-
dc.languageEnglish-
dc.publisherKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY-
dc.subjectHUMAN MELANOCYTES-
dc.subjectERK ACTIVATION-
dc.subjectIN-VITRO-
dc.subjectPIGMENTATION-
dc.subjectMELANOGENESIS-
dc.subjectTYROSINASE-
dc.titleKHG26792 Inhibits Melanin Synthesis in Mel-Ab Cells and a Skin Equivalent Model-
dc.typeArticle-
dc.identifier.doi10.4196/kjpp.2014.18.3.249-
dc.description.journalClass1-
dc.identifier.bibliographicCitationKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, v.18, no.3, pp.249 - 254-
dc.citation.titleKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY-
dc.citation.volume18-
dc.citation.number3-
dc.citation.startPage249-
dc.citation.endPage254-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART001888595-
dc.identifier.wosid000337556200008-
dc.identifier.scopusid2-s2.0-84904362337-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaPhysiology-
dc.type.docTypeArticle-
dc.subject.keywordPlusHUMAN MELANOCYTES-
dc.subject.keywordPlusERK ACTIVATION-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusPIGMENTATION-
dc.subject.keywordPlusMELANOGENESIS-
dc.subject.keywordPlusTYROSINASE-
dc.subject.keywordAuthorERK-
dc.subject.keywordAuthorKHG26792-
dc.subject.keywordAuthorMelanogenesis-
dc.subject.keywordAuthorSkin equivalent-
dc.subject.keywordAuthorTyrosinase-
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KIST Article > 2014
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