化学
细胞毒性T细胞
K562细胞
谷胱甘肽
哌啶
立体化学
白血病
癌细胞
黑色素瘤
氧化应激
细胞毒性
部分
生物化学
体外
癌症
癌症研究
生物
免疫学
酶
遗传学
作者
Ramóna Madácsi,Iván Kanizsai,Liliána Z. Fehér,Márió Gyuris,Béla Ózsvári,András Erdélyi,János Wölfling,László G. Puskás
出处
期刊:Medicinal Chemistry
[Bentham Science Publishers]
日期:2013-08-01
卷期号:9 (7): 911-919
被引量:11
标识
DOI:10.2174/1573406411309070004
摘要
A 30-membered piperidine ring-fused aromatic sulfonamide library was synthetized, including N-arylsulfonyl 1,2,3,4-tetrahydroquinolines, 1,2,3,4-tetrahydroisoquinolines and 2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indoles. The compounds induced oxidative stress and glutathione depletion in HT168 melanoma and K562 leukemia cells and in micromolar concentrations exerted cytotoxic effects. Among the tested sulfonamides, compounds 21, 22, 23, 35 and 41 exhibited 100% cytotoxic effects with low (< 10 µM) EC50 values on K562 cells. The cytotoxicity of lead compound 22 was investigated in 24 different cancer cell lines, and it was found to be active against leukemia, melanoma, glioblastoma, and liver, breast and lung cancer cells, as confirmed by classical biochemical and holographic microscopic analyses.
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