Kaczmarek L, Peczyńska-Czoch W, Opolski A, Wietrzyk J, Marcinkowska E, Boratyński J, Osiadacz J
Pharmaceutical Research Institute, Warszawa, Poland.
Anticancer Res. 1998 Jul-Aug;18(4C):3133-8.
New members of the cytotoxic indolo[2,3-b]quinoline family, with a methyl groups at N-5, N-6 (their presence stabilizes the positive charge of the molecule), were prepared using a modified Graebe-Ullmann reaction. The derivatives obtained were well soluble in water in a non-pH-dependent manner. They displayed strong antimicrobial activity against Gram-positive bacteria and pathogenic fungi (the MIC values fall between 0.0025 and 0.12 mM) and highly selective cytotoxicity in vitro against different human cancer cell lines: colon adenocarcinoma SW 707, lung carcinoma A 549, transitional cell carcinoma Hu 1703, and oral epidermoid carcinoma KB, in the range of 0.01 to 3.0 microM. They also stimulated the formation of topoisomerase-II-mediated DNA cleavage at concentration from 0.04 to 0.5 microM. These observations correspond well with the ability of the tested compounds to increase the melting temperature of calf thymus DNA (delta Tm being between 13 degrees C and 22 degrees C).
使用改良的格雷贝-乌尔曼反应制备了细胞毒性吲哚并[2,3 - b]喹啉家族的新成员,这些成员在N - 5、N - 6位带有甲基(它们的存在使分子的正电荷稳定)。所得到的衍生物以非pH依赖的方式很好地溶于水。它们对革兰氏阳性菌和致病真菌表现出强大的抗菌活性(最低抑菌浓度值在0.0025至0.12 mM之间),并且在体外对不同的人类癌细胞系具有高度选择性细胞毒性:结肠腺癌SW 707、肺癌A 549、移行细胞癌Hu 1703和口腔表皮样癌KB,范围为0.01至3.0 microM。它们还在0.04至0.5 microM的浓度下刺激拓扑异构酶II介导的DNA裂解的形成。这些观察结果与测试化合物提高小牛胸腺DNA解链温度的能力(ΔTm在13℃至22℃之间)非常吻合。