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三氮烯并氮茚的合成:一类具有抗肿瘤活性的新型三氮烯。

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

机构信息

Dipartimento di Scienze e Tecnologie Molecolari e Biomolecolari, Sezione di Chimica Farmaceutica e Biologica, Università degli Studi di Palermo, Via Archirafi 32, 90123 Palermo, Italy.

出版信息

ChemMedChem. 2011 Jul 4;6(7):1291-9. doi: 10.1002/cmdc.201100027. Epub 2011 Apr 26.

Abstract

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 5a-g and 6a-c were screened against a panel of human tumor cell lines, and two of them, 5e and 5f, 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.

摘要

尽管癌症的治疗和预防有所改善,但新诊断病例的数量仍在持续上升;这促使人们对开发新的有效化疗药物产生了浓厚的兴趣。三氮烯类化合物,如达卡巴嗪,已被用于许多癌症类型的临床治疗,包括脑癌、白血病和黑色素瘤。为了寻找新的增殖抑制剂,我们合成了具有三氮唑并氮杂吲哚骨架的新化合物。对 5a-g 和 6a-c 化合物进行了一系列人肿瘤细胞系的筛选,其中两种化合物 5e 和 5f 在所有细胞系中均表现出细胞毒性(GI(50)范围:2.2-8.2 μM)。这两种化合物甚至在一些多药耐药细胞系中仍保持其细胞毒性。流式细胞术分析表明,它们能够通过涉及溶酶体的细胞凋亡诱导细胞死亡。

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