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首页> 外文期刊>Angewandte Chemie >Versatile Synthetic Route to Cycloheximide and Analogues That Potently Inhibit Translation Elongation
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Versatile Synthetic Route to Cycloheximide and Analogues That Potently Inhibit Translation Elongation

机译:与环己酰亚胺和类似物的多功能合成途径,类似于翻译伸长的类似物

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摘要

Cycloheximide (CHX) is an inhibitor of eukaryotic translation elongation that has played an essential role in the study of protein synthesis. Despite its ubiquity, few studies have been directed towards accessing synthetic CHX derivatives, even though such efforts may lead to protein synthesis inhibitors with improved or alternate properties Described here is the total synthesis of CHX and analogues; and the establishment of structure-activity relationships (SA R) responsible for translation inhibition. The SAR studies aided the design of more potent compounds; one of which irreversibly blocks ribosomal elongation, preserves polysome profiles and may be a broadly useful tool for investigating protein synthesis.
机译:环己酰亚胺(CHX)是真核翻译伸长症的抑制剂,其在蛋白质合成的研究中发挥了重要作用。 尽管其难以理解,但甚至甚至涉及涉及这种努力可能导致蛋白质合成抑制剂的蛋白质合成抑制剂,这里描述的蛋白质合成抑制剂是CHX和类似物的总合成; 并建立了对翻译抑制的结构 - 活动关系(SA R)。 SAR研究辅助设计更有效的化合物; 其中一种不可逆转地阻断核糖体伸长率,保留了多瘤谱,并且可以是用于研究蛋白质合成的广义有用的工具。

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