A novel norneolignan glycoside and four new phenolic glycosides from the stems of Viburnum fordiae Hance

Author:

Chen Jia12,Shao Jianhua1,Zhao Chunchao2,Dong Ziling3,Shen Jie4,Liu Wenyan4,Zhao Min5,Fan Judi6

Affiliation:

1. 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: +86-514-87979054

2. College of Bioscience and Biotechnology , Yangzhou University , Yangzhou 225009 , P.R. China , Phone: +86-514-87991556

3. College of Bioscience and Biotechnology , Yangzhou University , Yangzhou 225009 , P.R. China

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

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 A novel norneolignan glycoside (1), categorized as an unusual 7-noraryl-4′,7-epoxy-8,5′-neolignan glycoside, four new phenolic glycosides (2–5), and a known neolignan glycoside (6) have been isolated from the ethanolic extract of the stems of Viburnum fordiae Hance. Dried stems of V. fordiae were extracted with 95% ethanol, and the concentrated extract was portioned successively with petroleum ether, ethyl acetate and n-butanol. The n-butanol portion was subjected to the macroporous resin HPD-100, silica gel, octadecyl SiO2, MCI gel and Sephadex LH-20 columns to obtain six compounds. Their structures including absolute configurations were determined by spectroscopic data [1H and 13C nuclear magnetic resonance (NMR), total correlation spectroscopy (TOCSY), heteronuclear single quantum coherence (HSQC), heteronuclear multiple-bond correlation (HMBC) and optical rotatory dispersion (ORD)] and chemical methods.

Publisher

Walter de Gruyter GmbH

Subject

Biomaterials

Reference31 articles.

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3. Fu, Q., Zan, K., Zhao, M.B., Zhou, S.X., Shi, S.P., Jiang, Y., Tu, P.F. (2010) Triterpene saponins from Clematis chinensis and their potential anti-inflammatory activity. J. Nat. Prod. 73:1234–1239.

4. Gao, H., Obanda, D.N., Shupe, T.F., Hse, C.Y., Ring, D.R. (2008) Antifungal activities of heartwood extracts of Port-Orford cedar extractives. Holzforschung 62:620–623.

5. Hudson, C.S., Dale, J.K. (1917) Studies on the forms of d-glucose and their mutarotation. J. Amer. Chem. Soc. 39:320–328.

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