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首页> 外文期刊>Tetrahedron >The Structural REquirements for Inhibition of Proteasome Function by the Lactacystin-Derived #beta#-Lactone and Synthetic Analogs
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The Structural REquirements for Inhibition of Proteasome Function by the Lactacystin-Derived #beta#-Lactone and Synthetic Analogs

机译:Lactacystin衍生的#beta#-内酯和合成类似物抑制蛋白酶体功能的结构要求。

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摘要

The synthesis of analogs of the lactacystin-derived #beta#-lactone (2) in which the substituents at C(5), C(7) and C(9) were systematically varied has led to a well defined structure-activity correlation for the highly selective inhibition of the mammalian 20 S proteasome.
机译:乳腺素衍生的#beta#-内酯(2)的类似物的合成,其中在C(5),C(7)和C(9)处的取代基被系统地改变了,从而导致对于对哺乳动物20 S蛋白酶体的高度选择性抑制。

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