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蛋白酶 3 膦酸抑制剂。

Proteinase 3 phosphonic inhibitors.

机构信息

Wroclaw University of Science and Technology, Faculty of Chemistry, Division of Medicinal Chemistry and Microbiology, Wybrzeże Wyspiańskiego 27, 50-370, Wrocław, Poland.

University of Gdansk, Faculty of Chemistry, Wita Stwosza 63, 80-308, Gdansk, Poland.

出版信息

Biochimie. 2019 Nov;166:142-149. doi: 10.1016/j.biochi.2019.03.005. Epub 2019 Mar 13.

Abstract

Neutrophils are one of the most important military services of the armed forces of the immune system, a crucial line of defense against bacterial or fungal onslaughts. One of their mechanisms of action relies on the production of serine proteases. One of these enzymes is proteinase 3 (PR3), which is engaged in the processing of pro-inflammatory cytokines, receptors, heat shock proteins and in the generation of antibacterial peptides. Despite its protective function, uncontrolled activity of PR3 has been associated with the progression of inflammation and tissue injury. Although PR3 was characterized at the beginning of 90's of the last century for the first time, the research on the development of its inhibitors is barely noticeable. Here we present the recent findings on the design, synthesis and the activity of phosphonic PR3 inhibitors together with the historical perspective.

摘要

中性粒细胞是免疫系统的最重要的军事力量之一,是抵御细菌或真菌侵袭的关键防线。它们的作用机制之一依赖于丝氨酸蛋白酶的产生。这些酶之一是蛋白酶 3(PR3),它参与前炎症细胞因子、受体、热休克蛋白的处理,并产生抗菌肽。尽管具有保护功能,但 PR3 的失控活性与炎症和组织损伤的进展有关。尽管 PR3 在 20 世纪 90 年代初首次被描述,但对其抑制剂的研究几乎没有被注意到。在这里,我们介绍了 PR3 膦酸抑制剂的设计、合成和活性的最新发现以及历史背景。

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