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渥曼青霉素的化学与生物学特性

Chemistry and biology of wortmannin.

作者信息

Wipf Peter, Halter Robert J

机构信息

Department of Chemistry, University of Pittsburgh, PA 15260, USA.

出版信息

Org Biomol Chem. 2005 Jun 7;3(11):2053-61. doi: 10.1039/b504418a. Epub 2005 Apr 20.

Abstract

Recent synthetic and biological studies of the viridin class of steroidal furans have revealed multiple opportunities for fundamental discoveries as well as advanced drug design. Wortmannin is a potent enzyme inhibitor that binds to the ATP site of important regulatory kinases such as PI-3 kinase and Polo-like kinase. The natural product shares a unique mechanism-based biological activation pathway with other viridins. Furthermore, while there have been several encouraging approaches toward the total synthesis of these compounds, there is still ample room for improvements in synthetic strategies and tactics, and the development of structurally simplified analogs that exert more specific biological effects and are devoid of toxicity issues that have thwarted the clinical development of the parent compounds.

摘要

近期对甾体呋喃类绿胶霉素的合成及生物学研究揭示了在基础发现以及先进药物设计方面的多种机遇。渥曼青霉素是一种强效酶抑制剂,可与重要的调节激酶(如PI-3激酶和Polo样激酶)的ATP位点结合。该天然产物与其他绿胶霉素类化合物共享独特的基于机制的生物激活途径。此外,尽管在这些化合物的全合成方面已经有了几种令人鼓舞的方法,但在合成策略和技巧方面仍有很大的改进空间,以及开发结构简化的类似物,这些类似物能发挥更特异的生物学效应,并且不存在阻碍母体化合物临床开发的毒性问题。

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