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靶向热休克蛋白 47 治疗特发性肺纤维化的抑制剂筛选。

Screening of Inhibitors Targeting Heat Shock Protein 47 Involved in the Development of Idiopathic Pulmonary Fibrosis.

机构信息

Department of Respiratory Medicine, Graduate School of Biomedical Sciences, Nagasaki University, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.

Center for Medical Innovation, Nagasaki University, 1-7-1 Sakamoto, Nagasaki, 852-8588, Japan.

出版信息

ChemMedChem. 2021 Aug 19;16(16):2515-2523. doi: 10.1002/cmdc.202100064. Epub 2021 May 19.

Abstract

Heat shock protein 47 (HSP47), a collagen-specific molecular chaperone, is causally related to fibrotic diseases, including idiopathic pulmonary fibrosis. The identification of Compounds that interfere with the HSP47-collagen interaction is essential for the development of relevant therapeutics. Herein, we prepared human HSP47 as a soluble fusion protein expressed in E. coli and established an assay system for HSP47 inhibitor screening. We screened a natural and synthetic Compound library established at Nagasaki University. Among 1023 Compounds, 13 exhibited inhibitory activity against human HSP47, of which three inhibited its function in a dose-dependent manner. Epigallocatechin-3-O-gallate, one of these three Compounds, is a typical polyphenol Compound derived from tea leaves. Structurally related Compounds were synthesized and examined for their activity, revealing a hydroxyl group at A-ring position 5 as important for its activity. The present findings provide valuable insight for the development of natural product-derived therapeutics for fibrotic diseases, including idiopathic pulmonary fibrosis.

摘要

热休克蛋白 47(HSP47)是一种胶原特异性分子伴侣,与包括特发性肺纤维化在内的纤维化疾病有因果关系。鉴定干扰 HSP47-胶原相互作用的化合物对于相关治疗药物的开发至关重要。在此,我们制备了可在大肠杆菌中表达的可溶性融合蛋白形式的人 HSP47,并建立了 HSP47 抑制剂筛选的测定系统。我们筛选了长崎大学建立的天然和合成化合物文库。在 1023 种化合物中,有 13 种表现出对人 HSP47 的抑制活性,其中 3 种以剂量依赖性方式抑制其功能。表没食子儿茶素-3-O-没食子酸酯(EGCG)是一种源自茶叶的典型多酚化合物,是这 3 种化合物之一。合成了结构相关的化合物并检查了它们的活性,结果表明 A 环 5 位的羟基对其活性很重要。这些发现为包括特发性肺纤维化在内的纤维化疾病的天然产物衍生治疗药物的开发提供了有价值的见解。

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