Inhibiting Inflammasomes with Small Molecules.

Q2 Medicine
Avril A B Robertson
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引用次数: 2

Abstract

Modulation of inflammasomes has tremendous therapeutic potential and is hotly pursued by industry and academia alike. Indeed a growing number of patents are emerging to protect the intellectual property in valuable compound classes. This chapter focusses specifically on the suite of small-molecule NLRP3 inflammasome inhibitors published, as specific modulation of other inflammasomes is not yet well established. Synthetic molecules, known drugs and natural product NLRP3 modulators will be detailed. Some of the molecular classes discussed have been extensively characterised through cell-based screening, pharmacokinetic profiling and therapeutic proof of concept animal models. However, many inhibitors lack rigorous studies and/or have multiple activities of which NLRP3 modulation is only one. While this is not intended as an exhaustive list, it should give an impression of the range of structures and strategies that are being used, alongside challenges encountered, in an effort to exploit the significant therapeutic benefits of targeting inflammasomes.

用小分子抑制炎性小体。
调节炎性小体具有巨大的治疗潜力,是工业界和学术界都在热烈追求的。事实上,越来越多的专利正在涌现,以保护有价值的化合物类别的知识产权。本章特别关注已发表的小分子NLRP3炎性小体抑制剂,因为其他炎性小体的特异性调节尚未很好地建立。将详细介绍合成分子、已知药物和天然产物NLRP3调节剂。通过基于细胞的筛选、药代动力学分析和概念动物模型的治疗证明,所讨论的一些分子类别已经得到了广泛的表征。然而,许多抑制剂缺乏严格的研究和/或具有多种活性,而NLRP3调节只是其中一种。虽然这并不是一个详尽的清单,但它应该给人一种正在使用的结构和策略的范围的印象,以及遇到的挑战,在努力利用靶向炎性小体的显着治疗益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Experientia supplementum (2012)
Experientia supplementum (2012) Medicine-Medicine (all)
CiteScore
3.30
自引率
0.00%
发文量
24
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