Spychała Jarosław
Department of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, 60-780 Poznań, Poland.
Bioorg Chem. 2008 Aug;36(4):183-9. doi: 10.1016/j.bioorg.2008.05.002. Epub 2008 Jun 20.
A series of related polycationic compounds has been screened for potential antitumor activity by the NCI's in vitro testing (one dose primary anticancer assay and the NCI-60 full panel screening). The GI50 values of triazines 3 and 4 are on average 1.9 microM and 2.4 microM, respectively. Furan 8 deserves mention too (1.9 microM). The biological test results showed that carbazole 10 possessed cytotoxic activity in the nanomolar range, much better than the other compounds tested, only against several cancer cell lines: CCRF-CEM, HL-60(TB), MOLT-4, NCI-H522, COLO 205, SF-268, but the average GI50 value was higher (15 microM). The activity appears closely dependent on the core-shape and length of the bisimidazoline molecules (important for both high cytotoxicity and DNA binding). The mechanism of DNA minor-groove binding of diamidines 1-12, based on the anticancer parameters, is highly probable.
美国国立癌症研究所通过体外测试(单剂量原发性抗癌测定和NCI - 60全组筛选)对一系列相关的聚阳离子化合物进行了潜在抗肿瘤活性筛选。三嗪3和4的半数生长抑制浓度(GI50)值平均分别为1.9微摩尔和2.4微摩尔。呋喃8也值得一提(1.9微摩尔)。生物学测试结果表明,咔唑10仅对几种癌细胞系具有纳摩尔范围内的细胞毒性活性,比其他测试化合物要好得多:CCRF - CEM、HL - 60(TB)、MOLT - 4、NCI - H522、COLO 205、SF - 268,但平均GI50值较高(15微摩尔)。该活性似乎紧密依赖于双咪唑啉分子的核心形状和长度(这对高细胞毒性和DNA结合都很重要)。基于抗癌参数,双脒1 - 12与DNA小沟结合的机制很可能成立。