Isolation of neolignan and phenolic glycosides from the branches of Viburnum macrocephalum f. keteleeri and their α-glucosidase inhibitory activity

Author:

Zhao Chunchao12ORCID,Chen Jia34,Shao Jianhua34,Shen Jie2,Xu Xiaoqing2,Li Kehuan1,Gu Wenyan1,Zhao Min5,Fan Judi6

Affiliation:

1. Joint International Research Laboratory of Agriculture and Agri-Product Safety of Ministry of Education of China , Yangzhou University , Yangzhou 225009 , P.R. China

2. Jiangsu Key Laboratory of Crop Genetics and Physiology/Co-Innovation Center for Modern Production Technology of Grain Crops , Yangzhou University , Yangzhou 225009 , P.R. China

3. Jiangsu Key Laboratory of Crop Genetics and Physiology/Co-Innovation Center for Modern Production Technology of Grain Crops , Yangzhou University , Yangzhou 225009 , P.R. China , Phone: +86-514-87991556

4. Jiangsu Key Laboratory of Crop Genetics and Physiology/Co-Innovation Center for Modern Production Technology of Grain Crops , Yangzhou University , Yangzhou 225009 , P.R. China , +86-514-87979054

5. School of Pharmacy , Shenyang Pharmaceutical University , Shenyang 110016 , P.R. China

6. School of Pharmacy , Guizhou Medical University , Guiyang 550004 , P.R. China

Abstract

Abstract Viburnum macrocephalum f. keteleeri, not well explored in the pharmaceutical field, is a tall deciduous shrub and commonly used as folk medicines for the treatment of type 2 diabetes (T2D). In this study, the dried branches of V. macrocephalum f. keteleeri were extracted with 95% ethanol and the extract was fractionated on the basis of polarity with ethyl acetate and n-butanol. Among the different fractions, the ethyl acetate fraction exhibited the highest α-glucosidase inhibitory activity, and its bioassay-guided fractionation led to the isolation and identification of six compounds including a new 8-O-4′-neolignan glycoside (1), categorized as a rare 7-deoxy skeleton, three previously undescribed phenolic glycosides (2–4), together with two known secondary metabolites (5, 6), which were found for the first time in Viburnum. Noticeably, compound 1 had almost the same intestinal α-glucosidase inhibitory activity as the positive control acarbose.

Funder

National Natural Science Foundation of China

Publisher

Walter de Gruyter GmbH

Subject

Biomaterials

Reference25 articles.

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