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Identification of compounds from chufa (Eleocharis dulcis) peels with inhibitory acrylamide formation activity
Nie, Hui; Huang, Shuangquan; Li, Xiaochun; Gong, Jixia; Wu, Fenglian; Yin, Jiaya; Liao, Yuemei; Wu, Shujie; Luo, Yanghe.
Afiliação
  • Nie, Hui; Hezhou University. Guangxi Talent Highland of Preservation and Deep Processing Research in Fruit and Vegetables. Hezhou. CN
  • Huang, Shuangquan; Hezhou University. Guangxi Talent Highland of Preservation and Deep Processing Research in Fruit and Vegetables. Hezhou. CN
  • Li, Xiaochun; Hezhou University. Guangxi Talent Highland of Preservation and Deep Processing Research in Fruit and Vegetables. Hezhou. CN
  • Gong, Jixia; Dalian Polytechnic University. School of Food Science and Technology. Dalian. CN
  • Wu, Fenglian; Dalian Polytechnic University. School of Food Science and Technology. Dalian. CN
  • Yin, Jiaya; Hezhou University. Guangxi Talent Highland of Preservation and Deep Processing Research in Fruit and Vegetables. Hezhou. CN
  • Liao, Yuemei; Hezhou University. Guangxi Talent Highland of Preservation and Deep Processing Research in Fruit and Vegetables. Hezhou. CN
  • Wu, Shujie; Hezhou University. Guangxi Talent Highland of Preservation and Deep Processing Research in Fruit and Vegetables. Hezhou. CN
  • Luo, Yanghe; Hezhou University. Guangxi Talent Highland of Preservation and Deep Processing Research in Fruit and Vegetables. Hezhou. CN
Rev. bras. farmacogn ; 29(4): 483-487, July-Aug. 2019. tab, graf
Article em En | LILACS | ID: biblio-1042276
Biblioteca responsável: BR1.1
ABSTRACT
Abstract Five compounds were isolated from the peels of chufa (Eleocharis dulcis (Burm.f.) Trin. ex Hensch., Cyperaceae). The chemical structures were determined by various spectroscopic analysis methods, including 1D and 2D NMR, and by comparison with literature data. All compounds were isolated for the first time from the peels of chufa. Compounds orcinol glucoside, leonuriside A, 2-hydroxymethyl-6-(5-hydroxy-2-methyl-phenoxy-methyl)-tetra-hydro-pyran-3,4,5-triol, and 1,4-dihydroxy-3-methoxy-phenyl-4-O-β-D-glucopyranoside showed good acrylamide formation activity, and acrylamide inhibition rates were 30.24, 32.81, 30.53, and 28.18%, respectively.
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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Tipo de estudo: Diagnostic_studies Idioma: En Revista: Rev. bras. farmacogn Assunto da revista: FARMACIA Ano de publicação: 2019 Tipo de documento: Article / Project document País de afiliação: China
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Tipo de estudo: Diagnostic_studies Idioma: En Revista: Rev. bras. farmacogn Assunto da revista: FARMACIA Ano de publicação: 2019 Tipo de documento: Article / Project document País de afiliação: China