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The Recent Development of Farnesyltransferase Inhibitors as Anticancer and Antimalarial Agents

机译:法尼基转移酶抑制剂作为抗癌和抗疟药的最新进展

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摘要

Cancer is a serious disease characterized by the uncontrolled growth division of cells, and nowadays it remains a significant challenge for the medical field. Malaria is an infectious disease in the similar situation to cancer. Almost 40% people in the world live in areas with malaria risk and each year there are about 2 to 3 million people dying from malaria. Farnesyltransferase (FTase) that belongs to isoprenyltransferase family can catalyze the initial step of Ras-processing and is identified as a promising target for the treatment of cancer and malaria. During the past decade years, a large number of FTase inhibitors with anticancer or antimalarial activity have been reported and some of them are undergoing clinical development. This review mainly introduces the FTase inhibitors as anticancer and antimalarial agents, with focus on their enzyme inhibitory activity, stability and enzyme selectivity, etc. In particular, the promising new FTase inhibitors among them will be discussed in detail and the inspirations for their design will be highlighted.
机译:癌症是一种严重的疾病,其特征在于细胞不受控制的生长分裂,如今,它仍然是医学领域的重大挑战。疟疾是一种与癌症相似的传染病。世界上将近40%的人生活在有疟疾风险的地区,每年约有2至300万人死于疟疾。属于异戊二烯基转移酶家族的法呢基转移酶(FTase)可以催化Ras加工的起始步骤,并且被确定为治疗癌症和疟疾的有希望的靶标。在过去的十年中,已经报道了许多具有抗癌或抗疟疾活性的FTase抑制剂,其中一些正在接受临床开发。这篇综述主要介绍了FTase抑制剂作为抗癌和抗疟药,重点是它们的酶抑制活性,稳定性和酶选择性等。特别是,将详细讨论其中有希望的新型FTase抑制剂,并为其设计灵感提供参考。突出显示。

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