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5-脂氧合酶作为药物靶点:抑制剂结构设计、SAR 和基于机制方法的趋势综述。

5-Lipoxygenase as a drug target: A review on trends in inhibitors structural design, SAR and mechanism based approach.

机构信息

Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore, Tamil Nadu 632014, India; Department of Biotechnology, Bhupat and Jyoti Mehta School of Biosciences, Indian Institute of Technology, Madras, Tamil Nadu 600036, India.

Department of Biotechnology, Bhupat and Jyoti Mehta School of Biosciences, Indian Institute of Technology, Madras, Tamil Nadu 600036, India.

出版信息

Bioorg Med Chem. 2019 Sep 1;27(17):3745-3759. doi: 10.1016/j.bmc.2019.06.040. Epub 2019 Jul 4.

Abstract

The most common inflammatory disease of the airways is asthma among children affecting around 235 million people worldwide. 5-Lipoxygenase (5-LOX) is a crucial enzyme which helps in the conversion of arachidonic acid (AA) to leukotrienes (LTs), the lipid mediators. It is associated with several inflammation related disorders such as asthma, allergy, and atherosclerosis. Therefore, it is considered as a promising target against inflammation and asthma. Currently, the only drug against 5-LOX which is available is Zileuton, while a few inhibitors are in clinical trial stages such as Atreleuton and Setileuton. So, there is a dire requirement in the area of progress of novel 5-LOX inhibitors which necessitates an understanding of their structure activity relationship and mode of action. In this review, novel 5-LOX inhibitors reported so far, their structural design, SAR and developmental strategies along with clinical updates are discussed over the last two decades.

摘要

气道最常见的炎症性疾病是儿童哮喘,全球约有 2.35 亿人受其影响。5-脂氧合酶(5-LOX)是一种关键酶,有助于将花生四烯酸(AA)转化为白三烯(LTs),即脂质介质。它与几种与炎症相关的疾病有关,如哮喘、过敏和动脉粥样硬化。因此,它被认为是一种有前途的抗炎和哮喘治疗靶点。目前,唯一可用于 5-LOX 的药物是齐留通,而一些抑制剂正处于临床试验阶段,如阿特留通和塞特留通。因此,在新型 5-LOX 抑制剂的研究领域存在迫切需求,这需要我们了解其结构活性关系和作用模式。在本篇综述中,讨论了过去二十年来报道的新型 5-LOX 抑制剂,包括它们的结构设计、SAR 和开发策略以及临床进展。

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