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Synthesis of triazenoazaindoles: a new class of triazenes with antitumor activity

机译:三氮杂氮杂吲哚的合成:一类具有抗肿瘤活性的新三氮烯

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摘要

Despite improvements in the treatment and prevention of cancer, the number of new diagnoses continues to rise; this has fuelled substantial interest in the development of new and effective chemotherapeutic agents. Compounds of the triazene class, such as dacarbazine, have been used in the clinical management of many cancer types including brain, leukemia, and melanoma. A new compound class bearing a triazenoazaindole scaffold was synthesized with the aim of identifying new antiproliferative agents. Compounds 5 a-g and 6 a-c were screened against a panel of human tumor cell lines, and two of them, 5 e and 5 f, showed cytotoxicity (GI(50) range: 2.2-8.2 μM) in all cell lines. These two compounds even maintained their cytotoxicity in some multidrug-resistant cell lines. Flow cytometry analysis demonstrated their ability to induce cell death by apoptosis with involvement of lysosomes.
机译:尽管在癌症的治疗和预防方面有所改进,但新诊断的数量仍在继续增加。这激发了人们对开发新型有效化疗药物的浓厚兴趣。三氮烯类化合物,例如达卡巴嗪,已用于许多癌症类型的临床管理,包括脑癌,白血病和黑素瘤。为了鉴定新的抗增殖剂,合成了带有三氮杂氮杂吲哚骨架的新的化合物类别。针对一组人类肿瘤细胞系筛选了化合物5 a-g和6 a-c,其中两个5 e和5 f在所有细胞系中均显示出细胞毒性(GI(50)范围:2.2-8.2μM)。这两种化合物甚至在某些具有多重耐药性的细胞系中保持了细胞毒性。流式细胞仪分析表明它们具有通过溶酶体参与细胞凋亡诱导细胞死亡的能力。

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