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The exploration of macrocycles for drug discovery--an underexploited structural class.用于药物发现的大环化合物探索——一类未被充分利用的结构类型。
Nat Rev Drug Discov. 2008 Jul;7(7):608-24. doi: 10.1038/nrd2590.
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Heat shock protein 90 inhibition in lung cancer.肺癌中的热休克蛋白90抑制作用
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Total synthesis of the Hsp90 inhibitor geldanamycin.热休克蛋白90(Hsp90)抑制剂格尔德霉素的全合成。
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Disruption of the Bcr-Abl/Hsp90 protein complex: a possible mechanism to inhibit Bcr-Abl-positive human leukemic blasts by novobiocin.Bcr-Abl/Hsp90蛋白复合物的破坏:新生霉素抑制Bcr-Abl阳性人白血病母细胞的一种可能机制。
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Recent Advances in the Study of hsp90 Structure and Mechanism of Action.hsp90 结构与作用机制研究的新进展
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Molecular characterization of macbecin as an Hsp90 inhibitor.作为一种热休克蛋白90(Hsp90)抑制剂的马贝西菌素的分子特征
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Designed TPR modules as novel anticancer agents.设计TPR模块作为新型抗癌剂。
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Proteomics of breast cancer: the quest for markers and therapeutic targets.乳腺癌蛋白质组学:寻找标志物和治疗靶点
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Development of novobiocin analogues that manifest anti-proliferative activity against several cancer cell lines.表现出对多种癌细胞系具有抗增殖活性的新生霉素类似物的开发。
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The Hsp90 molecular chaperone: an open and shut case for treatment.热休克蛋白90(Hsp90)分子伴侣:治疗的一个成败关键案例。
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热休克蛋白90(Hsp90)的天然产物抑制剂:药物研发的潜在先导物

Natural product inhibitors of Hsp90: potential leads for drug discovery.

作者信息

Amolins M W, Blagg B S J

机构信息

Department of Medicinal Chemistry, The University of Kansas, 1251 Wescoe Hall Drive, Malott 4070, Lawrence, Kansas 66045-7563, USA.

出版信息

Mini Rev Med Chem. 2009 Feb;9(2):140-52. doi: 10.2174/138955709787316056.

DOI:10.2174/138955709787316056
PMID:19200020
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2659174/
Abstract

Heat shock protein 90 has emerged as a promising target for the treatment of cancer and neurodegenerative diseases. This review summarizes recent advancements towards the development of natural products as they pertain to the biological and chemical understanding of this molecular chaperone.

摘要

热休克蛋白90已成为治疗癌症和神经退行性疾病的一个有前景的靶点。本综述总结了天然产物开发方面的最新进展,这些进展与对这种分子伴侣的生物学和化学理解有关。