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Synthesis and antitumor activity of 6- and 2- ( 1-acyl sulfanylalkyl)-5,8-dimethoxy- 1,4-naphthoquinones
作者姓名:Li Ming Zhao  ;Tian Pei Xie  ;YU Qin He  ;De Feng Xu  ;Shao Shun Li
作者单位:a School of Pharmacy, Shanghai Jiaotong University, 800 Dongchuan Road, Shanghai 200240, China;b Shanghai Standard Biotech Co. Ltd., 1011 Halei Road, Shanghai 201203, China
摘    要:Sixteen novel 6- and 2-(1-acylsulfanylalkyl)-5,8-dimethoxy-l,4-naphthoquinones were designed and synthesized. Their cytotoxicities were evaluated in vitro against BEL-7402, HT-29 and SPC-Al cell lines. The pharmacological results showed that most of the prepared compounds displayed the excellent selectivity for HT-29 cell line. Compound lab exhibited the most potent antitumor activity among the tested compounds.

关 键 词:5  8-二甲氧-l  4-萘醌  合成作用  抗癌作用  化学分析

Synthesis and antitumor activity of 6-and 2-(1-acylsulfanylalkyl)-5,8-dimethoxy-1,4-naphthoquinones
Li Ming Zhao,;Tian Pei Xie,;YU Qin He,;De Feng Xu,;Shao Shun Li.Synthesis and antitumor activity of 6-and 2-(1-acylsulfanylalkyl)-5,8-dimethoxy-1,4-naphthoquinones[J].Chinese Chemical Letters,2008,19(10):1206-1208.
Authors:Li Ming Zhao  Tian Pei Xie  Yu Qin He  De Feng Xu  Shao Shun Li
Institution:a School of Pharmacy, Shanghai Jiaotong University, 800 Dongchuan Road, Shanghai 200240, China;b Shanghai Standard Biotech Co. Ltd., 1011 Halei Road, Shanghai 201203, China
Abstract:Sixteen novel 6-and 2-(1-aeylsulfanylalkyl)-5,8-dimethoxy-1,4-naphthoquinones were designed and synthesized.Their eytotoxicifies were evaluated in vitro against BEL-7402,HT-29 and SPC-Al cell lines.The pharmacological results showed that most of the prepared compounds displayed the excellent selectivity for HT-29 cell line.Compound 16b exhibited the most potent antitumor activity among the tested compounds.
Keywords:5 8-Dimethoxy-1  4-naphthoquinone derivatives  Synthesis  Antimmor activity
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