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白三烯 C4 合酶:炎症的潜在药物靶点。

Leukotriene c4 synthase: upcoming drug target for inflammation.

机构信息

Bioengineering and Drug Design Lab, Department of Biotechnology, Indian Institute of Technology Madras, Chennai, India.

出版信息

Curr Drug Targets. 2012 Jul;13(8):1107-18. doi: 10.2174/138945012802009053.

Abstract

Leukotrienes are important mediators of pain and inflammation and they are produced in the arachidonic acid pathway via 5-lipoxygenase. They have been shown to have important roles in pyresis following antigen attack and in aspirin- intolerant asthma. They promote inflammation processes including eosinophil migration, increase in vascular permeability and bronchoconstriction. Hence, targeting the enzymes involved in the synthesis of these mediators can lead to the development of novel anti-inflammatory drugs. However, no drugs have yet been developed targeting leukotriene C4 synthase, a key enzyme leading to the synthesis of cysteinyl leukotrienes. The recent elucidation of its crystal structure now opens up the possibility of drugs against it. The inhibitors developed for this enzyme until now and the structural features responsible for their activity are discussed in this review. This understanding could lead to the design of new chemical entities.

摘要

白三烯是疼痛和炎症的重要介质,它们通过 5-脂氧合酶在花生四烯酸途径中产生。它们在抗原攻击后的发热和阿司匹林不耐受性哮喘中发挥重要作用。它们促进炎症过程,包括嗜酸性粒细胞迁移、血管通透性增加和支气管收缩。因此,针对这些介质合成中涉及的酶可以导致新型抗炎药物的开发。然而,目前还没有针对白三烯 C4 合酶的药物被开发出来,白三烯 C4 合酶是导致半胱氨酰白三烯合成的关键酶。其晶体结构的最新阐明现在为开发针对它的药物开辟了可能性。本文讨论了迄今为止为该酶开发的抑制剂及其负责其活性的结构特征。这种理解可能会导致新的化学实体的设计。

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