Planta Med 2008; 74(11): 1391-1396
DOI: 10.1055/s-2008-1081308
Natural Products Chemistry
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Minor Furofurano Lignans from the Tibetan Herb, Lancea tibetica

Ting Li1 , Xiao-Jiang Hao2 , Qian-Qun Gu1 , Wei-Ming Zhu1
  • 1Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao, P.R. China
  • 2The State Key Laboratory of Phytochemistry and Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, P. R. China
Further Information

Publication History

Received: January 3, 2008 Revised: May 28, 2008

Accepted: June 4, 2008

Publication Date:
29 July 2008 (online)

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Abstract

Four new furofurano lignans, lantibesides B – D (1 – 3) and lantibetin (4), along with nine known phenolic compounds were isolated from the EtOH extract of the traditional Tibetan medicinal plant, Lancea tibetica. By means of spectroscopic and chemical methods, the structures of the new compounds were elucidated as (1R,2S,5R,6S)-2-(3,4-methylenedioxyphenyl)-6-[(3-methoxy-4-β-D-xylopyranosyloxy(1→6)-β-D-glucopyranosyloxy)phenyl]-3,7-dioxabicyclo[3.3.0]octane (1), (1R,2R,5R,6S)-2-(3,4-methylenedioxyphenyl)-6-[(3-methoxy-4-β-D-xylopyranosyloxy(1→6)-β-D-glucopyranosyloxy)phenyl]-3,7-dioxabicyclo [3.3.0]octane (2), (1R,2R,5R,6S)-2-(3,4-methylenedioxyphenyl)-6-(3-methoxy-4-β-D-glucopyranosyloxy)phenyl-3,7-dioxabicyclo[3.3.0]octane (3), and (1R,2R,5R,6S)-2-(3,4-dimethoxyphenyl)-6-(3,4-dihydroxyphenyl)-3,7-dioxabicyclo[3.3.0] octane (4). Compounds 2 and 3 showed weak cytotoxicity against the HL-60 cell line with IC50 values of 61 and 99 μM, respectively.

References

Prof. Dr. Wei Ming Zhu

School of Medicine and Pharmacy

Ocean University of China

5# Yushan Road

Qingdao 266003

People’s Republic of China

Phone: +86-532-8203-2065

Fax: +86-532-8203-3054

Email: weimingzhu@ouc.edu.cn