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作为蛋白激酶抑制剂的雷夫霉素内酯,天然存在的毒素。

Resorcylic acid lactones as the protein kinase inhibitors , naturally occuring toxins.

机构信息

University Hospital Hradec Kralove, Biomedical Research Center, Sokolska 581, 50005 Hradec Kralove, Czech Republic.

出版信息

Mini Rev Med Chem. 2013 Nov;13(13):1873-8. doi: 10.2174/13895575113136660096.

Abstract

Resorcylic acid lactones (RALs) are polyketide natural products with a large macrocyclic ring fused to a resorcylic acid residue. Some RALs contain an α,β-unsaturated ketone in the macrocycle. So far 46 kinases have been identified that could be potentially targeted by this family of compounds. RALs are of interest for their modulation of growth, and tentatively for the treatment of cancer and neurodegenerative diseases. RALs containing a cis-enone are susceptible to Michael addition reactions with the cysteine residue in the kinase nucleotide binding site, and thus serve as potent inhibitors of several protein kinases - they therefore represent a unique pharmacophore. Notably, this moiety has been shown to be effective also in vivo. This mini-review focuses on the structure and biological effects of the most important RALs, namely zearalenone, hypothemycin, pochonins, lasiodiplodins, aigialomycins, cochlicomycins, zaenols, and paecilomycins. Finally, the review also deals with radicicol, which is a nanomolar inhibitor of the chaperone Hsp90, whose suppression leads to a combinatorial block of cancer-causing pathways.

摘要

雷锁辛内酯(RALs)是一类具有大环内酯结构的聚酮天然产物,其大环内酯结构与雷锁辛残基相连。一些 RALs 化合物的大环内酯结构中含有一个α,β-不饱和酮。迄今为止,已经鉴定出 46 种激酶,它们可能是这一类化合物的潜在作用靶点。由于 RALs 能够调节细胞生长,因此被认为具有治疗癌症和神经退行性疾病的潜力。含有顺式烯酮的 RALs 易与激酶核苷酸结合位点中的半胱氨酸残基发生迈克尔加成反应,因此它们是几种蛋白激酶的有效抑制剂,这使它们成为一种独特的药效团。值得注意的是,这一部分在体内也表现出了有效性。本综述主要聚焦于最重要的 RALs 化合物的结构和生物学效应,包括玉米赤霉烯酮、萎锈灵、波赛因、拉西多菌素、海鞘素、 Cochlicomycins、扎烯醇和多氧菌素。最后,该综述还讨论了雷迪霉素,它是一种纳摩尔级的热休克蛋白 90(Hsp90)抑制剂,其抑制作用会导致致癌途径的组合阻断。

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