ACAT inhibition of alkamides identified in the fruits of Piper nigrum

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dc.contributor.authorMun Chual Rho-
dc.contributor.authorSeung Woong Lee-
dc.contributor.authorHye Ran Park-
dc.contributor.authorJung Ho Choi-
dc.contributor.authorJi Yun Kang-
dc.contributor.authorK Kim-
dc.contributor.authorHyun Sun Lee-
dc.contributor.authorYoung Kook Kim-
dc.date.accessioned2017-04-19T09:06:46Z-
dc.date.available2017-04-19T09:06:46Z-
dc.date.issued2007-
dc.identifier.issn0031-9422-
dc.identifier.uri10.1016/j.phytochem.2006.11.025ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/7832-
dc.description.abstractIn this study, via a bioactivity-guided fractionation of MeOH extracts of the fruits of Piper nigrum, alkamide (5) and five previously-identified alkamides were isolated. Their structures were elucidated via spectroscopic analysis (1H, 13C NMR and ESI-MS), as follows: retrofractamide A (1), pipercide (2), piperchabamide D (3), pellitorin (4), dehydroretrofractamide C (5) and dehydropipernonaline (6). The IC50 values determined for the compounds were 24.5 (1), 3.7 (2), 13.5 (3), 40.5 (4), 60 (5) and 90 μM (6), according to the results of an ACAT enzyme assay system using rat liver microsomes. These compounds all inhibited cholesterol esterification in HepG2 cells.-
dc.publisherElsevier-
dc.titleACAT inhibition of alkamides identified in the fruits of Piper nigrum-
dc.title.alternativeACAT inhibition of alkamides identified in the fruits of Piper nigrum-
dc.typeArticle-
dc.citation.titlePhytochemistry-
dc.citation.number6-
dc.citation.endPage903-
dc.citation.startPage899-
dc.citation.volume68-
dc.contributor.affiliatedAuthorMun Chual Rho-
dc.contributor.affiliatedAuthorSeung Woong Lee-
dc.contributor.affiliatedAuthorHye Ran Park-
dc.contributor.affiliatedAuthorJung Ho Choi-
dc.contributor.affiliatedAuthorJi Yun Kang-
dc.contributor.affiliatedAuthorHyun Sun Lee-
dc.contributor.affiliatedAuthorYoung Kook Kim-
dc.contributor.alternativeName노문철-
dc.contributor.alternativeName이승웅-
dc.contributor.alternativeName박혜란-
dc.contributor.alternativeName최정호-
dc.contributor.alternativeName강지윤-
dc.contributor.alternativeName김관회-
dc.contributor.alternativeName이현선-
dc.contributor.alternativeName김영국-
dc.identifier.bibliographicCitationPhytochemistry, vol. 68, no. 6, pp. 899-903-
dc.identifier.doi10.1016/j.phytochem.2006.11.025-
dc.subject.keywordAcyl CoA: cholesterol acyltransferase (ACAT)-
dc.subject.keywordAlkamides-
dc.subject.keywordAtherosclerosis-
dc.subject.keywordCellular cholesterol esterification-
dc.subject.keywordHepG2 cells-
dc.subject.keywordPiper nigum L.-
dc.subject.keywordPiperaceae-
dc.subject.localACAT (acyl-CoA: cholesterol acyltransferase)-
dc.subject.localAcyl-CoA:cholesterol acyltransferase (ACAT)-
dc.subject.localcholesterol acytransferase (ACAT)-
dc.subject.localCholestrol Acyl Transferase (ACAT)-
dc.subject.localAcyl CoA: cholesterol acyltransferase (ACAT)-
dc.subject.localACAT (Acyl-CoA:cholesterol acyltransferase)-
dc.subject.localAcyl-CoA:cholesterol acyltransferase-
dc.subject.localACAT-
dc.subject.localAcyl-CoA: cholesterol acyltransferase-
dc.subject.localacyl-CoA:cholesterol acyltransferase (ACAT)-
dc.subject.localAcyl-CoA: cholesterol acyltransferase (ACAT)-
dc.subject.localAcyl-coenzyme A: cholesterol acyltransferase (ACAT)-
dc.subject.localCholesterol acytransferase (ACAT)-
dc.subject.localcholestrol acyl transferase (ACAT)-
dc.subject.localAlkamides-
dc.subject.localatherosclerosis-
dc.subject.localAtherosclerosis-
dc.subject.localatheroclerosis-
dc.subject.localCellular cholesterol esterification-
dc.subject.localHepG2 cells-
dc.subject.localHepG2 cell-
dc.subject.localPiper nigrum-
dc.subject.localPiper nigum L.-
dc.subject.localPiperaceae-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
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