化学
体外
曼尼奇基地
细胞培养
MTT法
基底细胞
癌症
癌
立体化学
癌症研究
组合化学
生物化学
有机化学
内科学
生物
医学
遗传学
作者
Wenli Lan,Jingchen Wei,Jiang-Ke Qin,Zhengmin Yang,Guifa Su,Dai Zhikai
出处
期刊:Letters in Drug Design & Discovery
[Bentham Science]
日期:2013-11-30
被引量:4
标识
DOI:10.2174/15701808113109990029
摘要
A novel series of Mannich bases of 1, 3-dihydroxyxanthone derivatives were designed and synthesized. The chemical structures of the compounds were characterized by IR, MS and NMR spectra. Their in vitro toxicities on six tu- mor cell lines including NCI-H460 (lung cancer), TCA-8113 (tongue squamous cell carcinomas), BEL-7402 (liver can- cer), HepG2 (hepatocarcinoma), SGC-7901 (gastric carcinoma) and T24 (urinary bladder carcinoma) were studied through MTT assay. The results showed that most of the compounds displayed mild to good inhibitory activities on the cancer cell lines. Some preliminary structure-activity relationships were also discussed.
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