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Chemical approaches to inhibitors of isoprenoid biosynthesis: targeting farnesyl and geranylgeranyl pyrophosphate synthases

机译:抑制类异戊二烯生物合成的化学方法:靶向法呢基和香叶基香叶基焦磷酸合成酶

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Post-translational lipid modifications farnesylation and geranylgeranylation of proteins (protein prenylation) have been identified to mediate critical events in cancer, cardiovascular disorders, malaria and bone disorders like osteoporosis. To date eight compounds are commercialized for the treatment of bone disorders, and there are considerable efforts to develop selective small molecules that inhibit protein prenylation. This review summarizes the approaches currently employed to synthesize new inhibitors of isoprenoid biosynthesis. Bisphosphonates are mainly prepared through reaction of carboxylic acids with phosphorus reagents, Michael addition to tetraethylvinylidenebisphosphonate and alkylation of tetralkylmethyl bisphosphonate. Approaches to non-bisphosphonate derivatives include a variety of methodologies depending on the structure of the target compound.
机译:翻译后脂质修饰蛋白的法呢基化和香叶基香叶基化(蛋白异戊二烯化)已被鉴定为介导癌症,心血管疾病,疟疾和骨疾病(如骨质疏松症)中的关键事件。迄今为止,已将八种化合物商业化用于治疗骨疾病,并且已经进行了相当大的努力来开发抑制蛋白质异戊二烯化的选择性小分子。这篇综述总结了目前用于合成类异戊二烯生物合成新抑制剂的方法。双膦酸酯主要是通过羧酸与磷试剂的反应,四乙基亚乙烯基双膦酸酯的迈克尔加成和四膦基甲基双膦酸酯的烷基化来制备的。根据目标化合物的结构,非双膦酸酯衍生物的方法包括多种方法。

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