标题:Recent Advances in The Discovery of N-Myristoyltransferase Inhibitors
作者:Zhao, Can;Ma, Shutao
作者机构:[Zhao, C] Department of Medicinal Chemistry, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Shandong U 更多
通讯作者:Zhao, C
通讯作者地址:[Zhao, C]Shandong Univ, Sch Pharmaceut Sci, Minist Educ, Dept Med Chem,Key Lab Chem Biol, 44 West Culture Rd, Jinan 250012, Peoples R China.
来源:ChemMedChem
出版年:2014
卷:9
期:11
页码:2425-2437
DOI:10.1002/cmdc.201402174
关键词:anticancer;antifungal;antiparasite;N-myristoyltransferase;structure-activity relationships
摘要:N-Myristoyltransferase (NMT) is a cytosolic monomeric enzyme present in eukaryotes such as fungi and protozoa, but is not found in prokaryotes. The attachment of a 14-carbon saturated fatty acid, myristate, from myristoyl-CoA (14:0 CoA) to the N-terminal glycine residue in a specific set of cellular proteins is commonly called protein N-myristoylation. The myristoylation reaction catalyzed by the enzyme myristoyl CoA:NMT is both necessary for the growth of various organisms and conclusive for cellular proliferation. Therefore, NMT has been identified as a novel and promising target for antifungal, antiparasitic, and anticancer agents, and a large number of potent NMT inhibitors with antifungal, antiparasitic, and anticancer activities have been reported. Herein we describe recent advances in the discovery of NMT inhibitors. We introduce not only the functions of NMT, but also some representative natural and synthetic inhibitors, with a focus on their biological activity, selectivity, and structure-activity relationship (SAR) information. In particular, inspiration from NMT inhibitor structures and the future direction of these compounds are highlighted.
收录类别:SCOPUS;SCIE
WOS核心被引频次:12
Scopus被引频次:12
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84927660467&doi=10.1002%2fcmdc.201402174&partnerID=40&md5=551e2682000881114dc0a43405a0da62
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