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dc.contributor.authorMesa Vanegas, Ana María-
dc.contributor.authorToro Suaza, Jhon Fredy-
dc.contributor.authorVásquez Cardona, Ana María-
dc.contributor.authorBlair Trujillo, Silvia-
dc.contributor.authorPeláez Jaramillo, Carlos-
dc.contributor.authorDíaz Oltra, Santiago-
dc.contributor.authorPachón, César Augusto-
dc.contributor.authorCarda, Miguel-
dc.date.accessioned2022-07-13T18:27:54Z-
dc.date.available2022-07-13T18:27:54Z-
dc.date.issued2018-
dc.identifier.citationAna María Mesa Vanegas, Jhon Fredy Toro Suaza, Ana María Vásquez Cardona, Silvia Blair Trujillo, Carlos Peláez Jaramill, Santiago Díaz Oltra, César Augusto Pachón, Miguel Carda, 2018. Antiplasmodial and cytotoxic activity of piper piedecuestanum Trel. and Yunck. Res. J. Med. Plants, 12: 57-64spa
dc.identifier.issn1819-3455-
dc.identifier.urihttps://hdl.handle.net/10495/29711-
dc.description.abstractABSTRACT: Background and Objective: Plasmodium resistance to antimalarial drugs has expanded and intensified, making new and effective antimalarial drugs urgently. The objective of this work was the in vitro evaluation of antiplasmodial activity of extracts of different polarity and compounds of the species P. piedecuestanum. Materials and Methods: The plant materials were obtained through successive extractions using solvents of different polarity such as hexane (H), dichloromethane (D), ethyl acetate (A) and methanol (M) and separations techniques for fractionation and isolation of compounds. The antiplasmodial activities of the extracts and compounds were evaluated by SYBR Green I® method and evaluated the cytotoxicity in the cell lines U-937, HUVEC by the MTT method. Results: The antiplasmodial and cytotoxic activity of the extracts of dichloromethane (PPD) and ethyl acetate (PPAE) with antiplasmodial activity of IC50 = 17.93 µg mLG1 ; IS = 2.093 and IC50 = 19.5 µg mLG1 ; IS = 0.791, respectively are reported for the first time. In addition, from P. piedecuestanum species were isolation and characterization five metabolites 5,8-Hydroxy-7-methoxyflavone(1), 6,7-dimethoxy-5,8- dihydroxyflavone(2), 6,7-dimethoxy-5-hydroxyflavone (mosloflavone) (3), 5,6-dihydroxy-7-methoxyflavone (negletein) (4), 5-hydroxy-7- methoxyflavone (5) and a brominated derivative from (5) named 6,8 bromo-5-hydroxy-7-methoxyflavone(7). Compound (1) presented promising antiplasmodial activity with an IC50 = 7.325 µg mLG1 (25.69 µM); ISHUVEC =13.65. Conclusion: Chemical analysis of extracts and compounds from P. piedecuestanum spices will play a central role in the development and modernization of an antimalarial herbal traditional in Colombia.spa
dc.format.extent8spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherAcademic Journalsspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-sa/2.5/co/*
dc.titleAntiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunckspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGrupo Interdisciplinario de Estudios Molecularesspa
dc.publisher.groupGrupo Malariaspa
dc.identifier.doi10.3923/rjmp.2018.57.64-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn2151-7924-
oaire.citationtitleResearch Journal of Medicinal Plantsspa
oaire.citationstartpage57spa
oaire.citationendpage64spa
oaire.citationvolume12spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-sa/4.0/spa
dc.publisher.placeNew York, Estados Unidosspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsPlasmodium falciparum-
dc.subject.proposalPiper pidecuestanumspa
dc.subject.proposalAntiplasmodial activityspa
dc.subject.proposalCytotoxic activityspa
dc.description.researchgroupidCOL0007524spa
dc.description.researchgroupidCOL0007462spa
dc.relation.ispartofjournalabbrevRes. J. Med. Plantsspa
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