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dc.contributor.authorNocedo Mena, Deyani
dc.contributor.authorRivas Galindo, Verónica M.
dc.contributor.authorNavarro Villaverde, Patricia
dc.contributor.authorGarza González, Elvira
dc.contributor.authorGonzález Maya, Leticia
dc.contributor.authorRíos, María Yolanda
dc.contributor.authorGarcía, Abraham
dc.contributor.authorÁvalos Alanís, Francisco G.
dc.contributor.authorRodríguez Rodríguez, José
dc.contributor.authorCamacho Corona, María del Rayo
dc.date.accessioned2021-02-09T09:28:49Z
dc.date.available2021-02-09T09:28:49Z
dc.date.issued2020-08
dc.identifier.citationHeliyon 6(8) : (2020) // Article ID e04671es_ES
dc.identifier.issn2405-8440
dc.identifier.urihttp://hdl.handle.net/10810/50111
dc.description.abstractCissus incisa is used in traditional Mexican medicine to treat certain ailments, infectious or cancerous diseases. Excepting for our previous research, this species had no scientific reports validating its traditional use. In this study, we evaluated the antibacterial and cytotoxic properties of the sphingolipids and others phytocompounds isolated from C. incisa leaves to increase the scientific knowledge of the Mexican flora. The antibacterial activity was evaluated against Gram-positive and Gram-negative bacteria by the Microdilution method. Meanwhile, the cytotoxic potential was determined on six human cancer cells: PC3, Hep3B, HepG2, MCF7, A549, and HeLa; using an aqueous solution cell proliferation assay kit. A cell line of immortalized human hepatocytes (IHH) was included as a control of non-cancerous cells. Selectivity index (SI) was determined only against the hepatocellular carcinoma cell lines. The phytochemical investigation of C. incisa leaves resulted in the isolation and characterization of five compounds: 2-(2'-hydroxydecanoyl amino)-1,3,4- hexadecanotriol-8-ene (1), 2,3-dihydroxypropyl tetracosanoate (2), beta-sitosterol-D-glucopyranoside (3), alpha-amyrin-3-O-beta-D-glucopyranoside (4), and a mixture of cerebrosides (5). Until now, this is the first report of the sphingolipids (1), (5-IV) and (5-V). Only the compound (4) and cerebrosides (5) exhibited antibacterial activity reaching a MIC value of 100 mu g/mL against Pseudomonas aeruginosa resistant to carbapenems. While, the acetylated derivate of (3), compound (3Ac) showed the best cytotoxic result against PC3 (IC50 = 43 +/- 4 mu g/mL) and Hep3B (IC50 = 49.0 +/- 4 mu g/mL) cancer cell lines. Likewise, (3Ac) achieved better SI values on HepG2 and Hep3B cell lines. This research reveals the importance of study medicinal plants, to identify bioactive molecules as sources of potential drugs. The presence of these compounds allows us to justify the use of this plant in traditional Mexican medicine.es_ES
dc.description.sponsorshipMaria del Rayo Camacho-Corona was supported by Universidad Autonoma de Nuevo Leon (04-093765-FAR-11/250-FCQ-UANL).es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectnatural product chemistryes_ES
dc.subjectcissus incisaes_ES
dc.subjecttraditional medicinees_ES
dc.subjectsphingolipidses_ES
dc.subjectantibacterial activityes_ES
dc.subjectcytotoxic activityes_ES
dc.subjectnatural-productses_ES
dc.subjectcancer-cellses_ES
dc.subjectapoptosises_ES
dc.subjectcerebrosideses_ES
dc.subjecttriterpeneses_ES
dc.subjectdiscoveryes_ES
dc.subjectbacteriaes_ES
dc.subjectacides_ES
dc.titleAntibacterial and cytotoxic activities of new sphingolipids and other constituents isolated from Cissus incisa leaveses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder©2020 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).es_ES
dc.rights.holderAtribución-NoComercial-SinDerivadas 3.0 España*
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S2405844020315152?via%3Dihubes_ES
dc.identifier.doi10.1016/j.heliyon.2020.e04671
dc.departamentoesQuímica orgánica IIes_ES
dc.departamentoeuKimika organikoa IIes_ES


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©2020 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Except where otherwise noted, this item's license is described as ©2020 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).