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Papain-Like Protease (PLpro) Inhibitory Effects of Cinnamic Amides from Tribulus terrestris Fruits

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dc.contributor.authorSong, Yeong Hun-
dc.contributor.authorKim, Dae Wook-
dc.contributor.authorCurtis-Long, Marcus John-
dc.contributor.authorYuk, Heung Joo-
dc.contributor.authorWang, Yan-
dc.contributor.authorZhuang, Ningning-
dc.contributor.authorLee, Kon Ho-
dc.contributor.authorJeon, Kwon Seok-
dc.contributor.authorPark, Ki Hun-
dc.date.accessioned2022-12-26T23:05:33Z-
dc.date.available2022-12-26T23:05:33Z-
dc.date.issued2014-06-
dc.identifier.issn0918-6158-
dc.identifier.issn1347-5215-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/18962-
dc.description.abstractTribulus terrestris fruits are well known for their usage in pharmaceutical preparations and food supplements. The methanol extract of T. terrestris fruits showed potent inhibition against the papain-like protease (PLpro), an essential proteolylic enzyme for protection to pathogenic virus and bacteria. Subsequent bioactivity-guided fractionation of this extract led to six cinnamic amides (1-6) and ferulic acid (7). Compound 6 emerged as new compound possessing the very rare carbinolamide motif. These compounds (1-7) were evaluated for severe acute respiratory syndrome coronavirus (SARS-CoV) PLpro inhibitory activity to identify their potencies and kinetic behavior. Compounds (1-6) displayed significant inhibitory activity with IC50 values in the range 15.8-70.1 mu M. The new cinnamic amide 6 was found to be most potent inhibitor with an IC50 of 15.8 mu M. In kinetic studies, all inhibitors exhibited mixed type inhibition. Furthermore, the most active PLpro inhibitors (1-6) were proven to be present in the native fruits in high quantities by HPLC chromatogram and liquid chromatography with diode array detection and electrospray ionization mass spectrometry (LC-DAD-ESI/MS).-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherPHARMACEUTICAL SOC JAPAN-
dc.titlePapain-Like Protease (PLpro) Inhibitory Effects of Cinnamic Amides from Tribulus terrestris Fruits-
dc.typeArticle-
dc.publisher.location일본-
dc.identifier.doi10.1248/bpb.b14-00026-
dc.identifier.scopusid2-s2.0-84901856638-
dc.identifier.wosid000336559200019-
dc.identifier.bibliographicCitationBIOLOGICAL & PHARMACEUTICAL BULLETIN, v.37, no.6, pp 1021 - 1028-
dc.citation.titleBIOLOGICAL & PHARMACEUTICAL BULLETIN-
dc.citation.volume37-
dc.citation.number6-
dc.citation.startPage1021-
dc.citation.endPage1028-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusVIRUS-
dc.subject.keywordAuthorpapain-like protease-
dc.subject.keywordAuthorTribulus terrestris-
dc.subject.keywordAuthorcinnamic amide-
dc.subject.keywordAuthorcarbinolamide-
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