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Title: Synthesis and anti-proliferative in-vitro activity of two natural dihydrostilbenes and their analogues. Author: Zhang WG, Zhao R, Ren J, Ren LX, Lin JG, Liu DL, Wu YL, Yao XS. Journal: Arch Pharm (Weinheim); 2007 May; 340(5):244-50. PubMed ID: 17516577. Abstract: A total synthetic route for two natural dihydrostilbenes with significant cytotoxicity toward human cancer cell lines, (3-(2-(7-methoxybenzo[d][1,3]dioxol-5-yl)ethyl)phenol 1a and 6-(3-hydroxyphenethyl)benzo[d][1,3]dioxol-4-ol 1b), which were isolated from Bulbophyllum odoratissimum Lindl, was developed via Wittig-Horner reaction. The natural products 1a and 1b were obtained in 28% and 20% overall yield, respectively. Additionally, nine analogues, 1c-1k, of the two natural dihydrostilbenes were synthesized and evaluated for their anti-proliferative activity against human SGC-7901, KB and HT-1080 cell lines by MTT assay. The activities of 1c and 1d were in the same range as those of the natural products 1a and 1b.[Abstract] [Full Text] [Related] [New Search]