Manolov I, Machulla H J, Momekov G
Department of Organic Chemistry, Faculty of Pharmacy, Medical University-Sofia, Bulgaria.
Pharmazie. 2006 Jun;61(6):511-6. doi: 10.1002/chin.200639088.
The synthesis, physicochemical characterization and preliminary pharmacological evaluation of the cytotoxic effects of two novel substances, 1-(4-benzoylphenyl)-3,3-dimethyltriazene and 1-(2-benzoylphenyl)-3,3-dimethyltriazene is presented. The cytotoxicity of the novel benzophenone-linked triazenes and of ten other 1-phenyl-3,3-dimethyl triazene derivatives as well as of the referent alkylating drug melphalan was assessed using the MTT-dye reduction assay. A panel of human tumor cell lines was used: the chronic lymphoid leukemia SKW-3, the acute promyelocyte leukemia HL-60 and its multi-drug-resistant subline HL-60/Dox. Both novel compounds showed strong cytotoxic activity, comparable to that of the referent alkylating agent melphalan, whereas the ten ring-substituted 1-phenyl-3,3-dimethyl triazenes proved to be far less active in vitro. DNA-fragmentation analysis indicated that after 24 h treatment the novel benzophenone-linked triazenes induced programmed cell death in HL-60 cells.
本文介绍了两种新型物质1-(4-苯甲酰基苯基)-3,3-二甲基三氮烯和1-(2-苯甲酰基苯基)-3,3-二甲基三氮烯的合成、理化特性及其细胞毒性作用的初步药理学评价。使用MTT染料还原试验评估了新型二苯甲酮连接的三氮烯、其他十种1-苯基-3,3-二甲基三氮烯衍生物以及参考烷基化药物美法仑的细胞毒性。使用了一组人类肿瘤细胞系:慢性淋巴细胞白血病SKW-3、急性早幼粒细胞白血病HL-60及其多药耐药亚系HL-60/Dox。两种新型化合物均表现出较强的细胞毒性活性,与参考烷基化剂美法仑相当,而十种环取代的1-苯基-3,3-二甲基三氮烯在体外的活性则低得多。DNA片段化分析表明,处理24小时后,新型二苯甲酮连接的三氮烯在HL-60细胞中诱导程序性细胞死亡。