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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.
  • 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 in English | LILACS | ID: biblio-1042276
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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Full text: Available Index: LILACS (Americas) Type of study: Diagnostic study Language: English Journal: Rev. bras. farmacogn Journal subject: Pharmacy Year: 2019 Type: Article / Project document Affiliation country: China Institution/Affiliation country: Dalian Polytechnic University/CN / Hezhou University/CN

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Full text: Available Index: LILACS (Americas) Type of study: Diagnostic study Language: English Journal: Rev. bras. farmacogn Journal subject: Pharmacy Year: 2019 Type: Article / Project document Affiliation country: China Institution/Affiliation country: Dalian Polytechnic University/CN / Hezhou University/CN