Carlos J Bethencourt-Estrella, Samuel Delgado-Hernández, Atteneri López-Arencibia, Irene Serafín-Pérez, Paula Rodríguez-Santana, Sara Rodríguez-Camacho, Carolina Fernández-Serafín, David Tejedor, Jacob Lorenzo-Morales, José E Piñero
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In addition, the drugs used to combat it were developed in the 1970s and present major toxicity problems and limited efficacy in the chronicity of the disease. This has led to research into new active compounds that are effective against the disease, with studies on cyanoderivatives showing promising activity. In this work, eight active <i>E</i>-cyanoacrylamides/5-imino pyrrolones were studied. Compounds B and F showed excellent activity, while compounds C and G stood out for their lower cytotoxicity. After correlating the activity and cytotoxicity of the compounds, it was observed that compounds B, C, and G obtained the most favourable results. 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引用次数: 0
摘要
南美锥虫病是由一种名为南美锥虫的原生寄生虫引起的。感染后的第一阶段为临床期,通常无症状或表现出非特异性症状;第二阶段为慢性期,部分患者会出现心脏和消化系统功能障碍。这种疾病影响着 700 万人,被世界卫生组织列为被忽视的热带疾病。此外,用于防治这种疾病的药物是在 20 世纪 70 年代开发的,存在严重的毒性问题,对慢性病的疗效有限。因此,人们开始研究能有效防治该疾病的新活性化合物,其中对氰基二元化合物的研究显示出了良好的活性。这项工作研究了八种活性 E-氰基丙烯酰胺/5-亚氨基吡咯烷酮。化合物 B 和 F 显示出卓越的活性,而化合物 C 和 G 则因细胞毒性较低而脱颖而出。在对化合物的活性和细胞毒性进行相关分析后,发现化合物 B、C 和 G 的结果最为理想。对这些化合物进行了各种细胞死亡研究,结果表明,所有这些化合物都能产生程序性细胞死亡,其中化合物 B 的细胞死亡阶段较晚。
E-Cyanoacrylamides and 5-Imino Pyrrolones against Trypanosoma cruzi: Activity and Induced Mechanisms of Cell Death.
Chagas disease is caused by a protozoan parasite called Trypanosoma cruzi. The infection produces a first clinical phase, commonly asymptomatic or showing non-specific symptoms, and a second chronic phase characterized by cardiac and digestive dysfunctions in some individuals with the disease. This disease affects 7 million people and has been categorized by the World Health Organisation as a neglected tropical disease. In addition, the drugs used to combat it were developed in the 1970s and present major toxicity problems and limited efficacy in the chronicity of the disease. This has led to research into new active compounds that are effective against the disease, with studies on cyanoderivatives showing promising activity. In this work, eight active E-cyanoacrylamides/5-imino pyrrolones were studied. Compounds B and F showed excellent activity, while compounds C and G stood out for their lower cytotoxicity. After correlating the activity and cytotoxicity of the compounds, it was observed that compounds B, C, and G obtained the most favourable results. Various cell death studies were carried out with these compounds, and it was determined that all of them produced programmed cell death, with compound B standing out as being at a late stage in the process.