首页> 美国卫生研究院文献>Molecules >NAMI-A and KP1019/1339 Two Iconic Ruthenium Anticancer Drug Candidates Face-to-Face: A Case Story in Medicinal Inorganic Chemistry
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NAMI-A and KP1019/1339 Two Iconic Ruthenium Anticancer Drug Candidates Face-to-Face: A Case Story in Medicinal Inorganic Chemistry

机译:NAMI-A和KP1019 / 1339面对面的两个标志性钌抗癌候选药物:药物无机化学中的案例

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摘要

NAMI-A ((ImH)[trans-RuCl4(dmso-S)(Im)], Im = imidazole) and KP1019/1339 (KP1019 = (IndH)[trans-RuCl4(Ind)2], Ind = indazole; KP1339 = Na[trans-RuCl4(Ind)2]) are two structurally related ruthenium(III) coordination compounds that have attracted a lot of attention in the medicinal inorganic chemistry scientific community as promising anticancer drug candidates. This has led to a considerable amount of studies on their respective chemico-biological features and to the eventual admission of both to clinical trials. The encouraging pharmacological performances qualified KP1019 mainly as a cytotoxic agent for the treatment of platinum-resistant colorectal cancers, whereas the non-cytotoxic NAMI-A has gained the reputation of being a very effective antimetastatic drug. A critical and strictly comparative analysis of the studies conducted so far on NAMI-A and KP1019 allows us to define the state of the art of these experimental ruthenium drugs in terms of the respective pharmacological profiles and potential clinical applications, and to gain some insight into the inherent molecular mechanisms. Despite their evident structural relatedness, deeply distinct biological and pharmacological profiles do emerge. Overall, these two iconic ruthenium complexes form an exemplary and unique case in the field of medicinal inorganic chemistry.
机译:NAMI-A((ImH)[反式RuCl4(dmso-S)(Im)],Im =咪唑)和KP1019 / 1339(KP1019 =(IndH)[反式RuCl4(Ind)2],Ind =吲唑; KP1339 Na [反式RuCl4(Ind)2])是两种结构相关的钌(III)配位化合物,已在药用无机化学科学界引起了广泛关注,成为有前途的抗癌药物候选物。这导致对它们各自的化学生物学特性进行了大量研究,并最终使两者都进入了临床试验。令人鼓舞的药理性能使KP1019主要用作治疗铂类耐药性结直肠癌的细胞毒性剂,而无细胞毒性的NAMI-A已获得了非常有效的抗转移药物的声誉。通过对迄今为止对NAMI-A和KP1019进行的研究进行严格且严格的比较分析,我们可以根据各自的药理学特征和潜在的临床应用来定义这些实验性钌药物的技术水平,并获得对固有的分子机制。尽管它们具有明显的结构相关性,但确实出现了截然不同的生物学和药理学特征。总体而言,这两种标志性的钌络合物在药用无机化学领域构成了一个典范且独特的案例。

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