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Insecticidal and α-glucosidase inhibitory activities of chemical constituents from Viburnum fordiae Hance.
Shao, Jian-Hua; Chen, Jia; Zhao, Chun-Chao; Shen, Jie; Liu, Wen-Yan; Gu, Wen-Yan; Li, Ke-Huan.
Afiliação
  • Shao JH; a Jiangsu Key Laboratory of Crop Genetics and Physiology/Co-Innovation Center for Modern Production Technology of Grain Crops , Yangzhou University , Yangzhou , China.
  • Chen J; a Jiangsu Key Laboratory of Crop Genetics and Physiology/Co-Innovation Center for Modern Production Technology of Grain Crops , Yangzhou University , Yangzhou , China.
  • Zhao CC; a Jiangsu Key Laboratory of Crop Genetics and Physiology/Co-Innovation Center for Modern Production Technology of Grain Crops , Yangzhou University , Yangzhou , China.
  • Shen J; b Joint International Research Laboratory of Agriculture & Agri-Product Safety of Ministry of Education of China , Yangzhou University , Yangzhou , China.
  • Liu WY; b Joint International Research Laboratory of Agriculture & Agri-Product Safety of Ministry of Education of China , Yangzhou University , Yangzhou , China.
  • Gu WY; b Joint International Research Laboratory of Agriculture & Agri-Product Safety of Ministry of Education of China , Yangzhou University , Yangzhou , China.
  • Li KH; a Jiangsu Key Laboratory of Crop Genetics and Physiology/Co-Innovation Center for Modern Production Technology of Grain Crops , Yangzhou University , Yangzhou , China.
Nat Prod Res ; 33(18): 2662-2667, 2019 Sep.
Article em En | MEDLINE | ID: mdl-29703100
ABSTRACT
The ethanolic extract of the stems of Viburnum fordiae Hance showed insecticidal and α-glucosidase inhibitory activities and then was fractionated by bioactivity-guided fractionation to obtain a rare C13-norisoprenoid (1), together with a new phenolic glycoside (2), and seven known compounds, alangionoside C (3), pisumionoside (4), koaburaside (5), 3,5-dimethoxy-benzyl alcohol 4-O-ß-d-glucopyranoside (6), 3,4,5-trimethoxybenzyl-ß-d-glucopyranoside (7), arbutin (8), and salidroside (9). The previously undescribed compounds were elucidated as (3R,9R)-3-hydroxy-7,8-didehydro-ß-ionyl 9-O-α-d-arabinopyranosyl-(1→6)-ß-d-glucopyranoside (1) and 2-(4-O-ß-d-glucopyranosyl)syringylpropane-1,3-diol (2) by spectroscopic data (1H and 13C NMR, HSQC, HMBC, 1H-1H COSY, HSQC-TOCSY, HRESIMS, IR and ORD) and chemical methods. Compound 1 showed potent insecticidal effect against Mythimna separata with LD50 value of 140 µg g-1. Compounds 2, 5, 6, 8 and 9 showed varying α-glucosidase inhibitory activity with IC50 values ranging from 148.2 to 230.9 µM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Viburnum / Inibidores de Glicosídeo Hidrolases / Inseticidas Limite: Animals Idioma: En Revista: Nat Prod Res Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Viburnum / Inibidores de Glicosídeo Hidrolases / Inseticidas Limite: Animals Idioma: En Revista: Nat Prod Res Ano de publicação: 2019 Tipo de documento: Article