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Bioactive terpenoid constituents from Eclipta prostrata.
Yu, Shu-Juan; Yu, Jin-Hai; Yu, Zhi-Pu; Yan, Xue; Zhang, Jun-Sheng; Sun, Jin-Yue; Zhang, Hua.
Affiliation
  • Yu SJ; School of Chemistry and Chemical Engineering, University of Jinan, 336 West Road of Nan Xinzhuang, Jinan 250022, China; School of Biological Science and Technology, University of Jinan, 336 West Road of Nan Xinzhuang, Jinan 250022, China.
  • Yu JH; School of Biological Science and Technology, University of Jinan, 336 West Road of Nan Xinzhuang, Jinan 250022, China.
  • Yu ZP; School of Chemistry and Chemical Engineering, University of Jinan, 336 West Road of Nan Xinzhuang, Jinan 250022, China; School of Biological Science and Technology, University of Jinan, 336 West Road of Nan Xinzhuang, Jinan 250022, China.
  • Yan X; School of Chemistry and Chemical Engineering, University of Jinan, 336 West Road of Nan Xinzhuang, Jinan 250022, China; School of Biological Science and Technology, University of Jinan, 336 West Road of Nan Xinzhuang, Jinan 250022, China.
  • Zhang JS; School of Biological Science and Technology, University of Jinan, 336 West Road of Nan Xinzhuang, Jinan 250022, China.
  • Sun JY; Institute of Agro-Food Science and Technology, Shandong Academy of Agricultural Sciences, 202 Gongye North Road, Jinan 250100, China.
  • Zhang H; School of Biological Science and Technology, University of Jinan, 336 West Road of Nan Xinzhuang, Jinan 250022, China. Electronic address: bio_zhangh@ujn.edu.cn.
Phytochemistry ; 170: 112192, 2020 Feb.
Article in En | MEDLINE | ID: mdl-31726325
ABSTRACT
Chemical fractionation of the ethanolic extract of Eclipta prostrata yielded a series of unreported terpenoid constituents, including a rare 6/6/6/6-fused tetracyclic triterpenoid, a pentacyclic triterpenoid, two pentacyclic triterpenoid saponins, a diterpenoid and a sesquiterpenoid. Structures were assigned to these compounds on the basis of comprehensive spectroscopic analyses, with the absolute configurations of the tetracyclic triterpenoid, the diterpenoid and the sesquiterpenoid being determined via explanation of electronic circular dichroism data. Screening of these isolates in an array of bioassays revealed antibacterial, cytotoxic and α-glucosidase inhibitory activities for selective compounds. Of particular interest, the tetracyclic triterpenoid showed very strong inhibition against α-glucosidase with an IC50 of 0.82 ±â€¯0.18 µM, being 103-fold as active as the positive control acarbose.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Terpenes / Plant Extracts / Eclipta / Phytochemicals / Glycoside Hydrolase Inhibitors / Anti-Bacterial Agents / Neoplasms Limits: Humans Language: En Journal: Phytochemistry Year: 2020 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Terpenes / Plant Extracts / Eclipta / Phytochemicals / Glycoside Hydrolase Inhibitors / Anti-Bacterial Agents / Neoplasms Limits: Humans Language: En Journal: Phytochemistry Year: 2020 Document type: Article Affiliation country: China
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