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DOI: 10.1055/s-0028-1112212
© Georg Thieme Verlag KG Stuttgart · New York
Phenylpropanoid and Lignan Derivatives from Antiaris toxicaria and their Effects on Proliferation and Differentiation of an Osteoblast-Like Cell Line
Publication History
Received: January 25, 2008
Revised: October 28, 2008
Accepted: November 4, 2008
Publication Date:
30 January 2009 (online)
Abstract
Antiarisin A and B (1 and 2), together with seventeen known compounds (3 – 19), were isolated from the EtOAc extract of the stem of Antiaris toxicaria Lesch. Their structures were determined on the basis of spectroscopic analyses and chemical methods. Most of the compounds were reported for the first time from the Antiaris genus and firstly studied for their proliferative and differentiative activity on osteoblast-like cells. Screening results indicated that, at the concentration of 10 – 8 M, benzofuran lignans 5, 6, 11 and 13 could significantly stimulate the proliferation of UMR106 cells, while 8, 9, 11, 14, 15 and 17 could enhance ALP (alkaline phosphatase) activity.
Key words
Antiaris toxicaria Lesch (Moraceae) - phenylpropanoids - lignans - anti-osteoporosis - UMR106 cells - alkaline phosphatase (ALP)
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Prof. Xin-Sheng Yao
Institute of Traditional Chinese Medicine & Natural Products
Jinan University
Guangzhou 510632
People's Republic of China
Phone: +86-20-8522-5849
Fax: +86-20-8522-1559
Email: yaoxinsheng@vip.tom.com
Dr. Xue Zhang
College of Traditional Chinese Medicine
Shenyang Pharmaceutical University
Shenyang 110016
People's Republic of China
Email: zxalice@sohu.com
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