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Trypanocidal Activity of Flavokawin B, a Component of Polygonum ferrugineum Wedd.
Rodrigues, Danilo F; Maniscalco, David A; Silva, Flavia A J; Chiari, Bruna G; Castelli, María V; Isaac, Vera L B; Cicarelli, Regina M B; López, Silvia N.
Afiliação
  • Rodrigues DF; Department of Biological Sciences, School of Pharmaceutical Sciences of Araraquara, São Paulo State University, Araraquara, Brazil.
  • Maniscalco DA; Universidad Nacional de Rosario, CONICET, Farmacognosia, Facultad de Ciencias Bioquímicas y Farmacéuticas, Rosario, Argentina.
  • Silva FA; Department of Biological Sciences, School of Pharmaceutical Sciences of Araraquara, São Paulo State University, Araraquara, Brazil.
  • Chiari BG; Department of Drugs and Medicaments, School of Pharmaceutical Sciences of Araraquara, São Paulo State University, Araraquara, Brazil.
  • Castelli MV; Universidad Nacional de Rosario, CONICET, Farmacognosia, Facultad de Ciencias Bioquímicas y Farmacéuticas, Rosario, Argentina.
  • Isaac VL; Department of Drugs and Medicaments, School of Pharmaceutical Sciences of Araraquara, São Paulo State University, Araraquara, Brazil.
  • Cicarelli RM; Department of Biological Sciences, School of Pharmaceutical Sciences of Araraquara, São Paulo State University, Araraquara, Brazil.
  • López SN; Universidad Nacional de Rosario, CONICET, Farmacognosia, Facultad de Ciencias Bioquímicas y Farmacéuticas, Rosario, Argentina.
Planta Med ; 83(3-04): 239-244, 2017 Feb.
Article em En | MEDLINE | ID: mdl-27442262
The trypanocidal potential of the natural chalcone flavokawin B, which was isolated from the hexanic extract of Polygonum ferrugineum Wedd., is reported here. Although flavokawin B is widespread, this is the first report about its trypanocidal properties on both Trypanosoma cruzi (IC50 = 9.5 µM, IC50 = 34.7 µM benznidazol, Y strain) epimastigotes and Trypanosoma brucei (IC50 = 4.8 µM, IC50 = 6.4 µM pentamidine, 29-13 strain) procyclic forms, which was also corroborated on T. brucei strain 427 (IC50 = 6.2 µM). In order to learn more about its properties, unspecific cytotoxicity on Hep G2 cells was investigated as well as the trans-splicing inhibitory potential on T. brucei cells. The results shown here point to flavokawin B as a candidate in the search for new agents. It is also cheaper and less toxic than the available drugs to treat trypanosomiasis with a special focus on sleeping sickness disease.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tripanossomicidas / Trypanosoma brucei brucei / Trypanosoma cruzi / Tripanossomíase / Flavonoides Limite: Humans Idioma: En Revista: Planta Med Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tripanossomicidas / Trypanosoma brucei brucei / Trypanosoma cruzi / Tripanossomíase / Flavonoides Limite: Humans Idioma: En Revista: Planta Med Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Brasil