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基于结构的药物重新定位:潜力与局限。

Structure-based drug repositioning: Potential and limits.

作者信息

Adasme Melissa F, Parisi Daniele, Sveshnikova Anastasia, Schroeder Michael

机构信息

Biotechnology Center (BIOTEC), Technische Universität Dresden, 01307 Dresden, Germany.

Biotechnology Center (BIOTEC), Technische Universität Dresden, 01307 Dresden, Germany; ESAT-STADIUS, KU Leuven, B-3001 Heverlee, Belgium.

出版信息

Semin Cancer Biol. 2021 Jan;68:192-198. doi: 10.1016/j.semcancer.2020.01.010. Epub 2020 Feb 4.

Abstract

Drug repositioning, the assignment of new therapeutic purposes to known drugs, is an established strategy with many repurposed drugs on the market and many more at experimental stage. We review three use cases, a herpes drug with benefits in cancer, a cancer drug with potential in autoimmune disease, and a selective and an unspecific drug binding the same target (GPCR). We explore these use cases from a structural point of view focusing on a deep understanding of the underlying drug-target interactions. We review tools and data needed for such a drug-centric structural repositioning approach. Finally, we show that the availability of data on targets is an important limiting factor to realize the full potential of structural drug-repositioning.

摘要

药物重新定位,即将已知药物用于新的治疗目的,是一种既定策略,市场上已有许多重新定位的药物,还有更多处于实验阶段。我们回顾了三个用例,一种对癌症有益的疱疹药物、一种对自身免疫性疾病有潜力的癌症药物,以及两种结合相同靶点(GPCR)的选择性和非特异性药物。我们从结构角度探讨这些用例,重点深入了解潜在的药物-靶点相互作用。我们回顾了这种以药物为中心的结构重新定位方法所需的工具和数据。最后,我们表明靶点数据的可用性是实现结构药物重新定位全部潜力的一个重要限制因素。

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