Recent update on anti-dengue drug discovery

被引:46
|
作者
Dighe, Satish N. [1 ]
Ekwudu, O'mezie [1 ]
Dua, Kamal [2 ]
Chellappan, Dinesh Kumar [3 ]
Katavic, Peter L. [1 ]
Collet, Trudi A. [1 ]
机构
[1] Queensland Univ Technol, Sch Clin Sci, Inst Hlth & Biomed Innovat, Innovat Med Grp, Brisbane, Qld, Australia
[2] Univ Technol Sydney, Grad Sch Hlth, Discipline Pharm, Ultimo, Australia
[3] Int Med Univ, Sch Pharm, Dept Life Sci, Kuala Lumpur 57000, Malaysia
关键词
Dengue; DENV; NS3; NS4; NS5; Natural product; Synthesis; HTS; HTVS; WEST-NILE-VIRUS; DEPENDENT RNA-POLYMERASE; BETA-CARBOLINE DERIVATIVES; SMALL-MOLECULE INHIBITORS; SINGLE-AMINO-ACID; ANTIVIRAL ACTIVITY; TARGETING DENGUE; CRYSTAL-STRUCTURE; SERINE-PROTEASE; NONNUCLEOSIDE INHIBITORS;
D O I
10.1016/j.ejmech.2019.05.010
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Dengue is the most important arthropod-borne viral disease of humans, with more than half of the global population living in at-risk areas. Despite the negative impact on public health, there are no antiviral therapies available, and the only licensed vaccine, Dengvaxia (R), has been contraindicated in children below nine years of age. In an effort to combat dengue, several small molecules have entered into human clinical trials. Here, we review anti-DENV molecules and their drug targets that have been published within the past five years (2014-2018). Further, we discuss their probable mechanisms of action and describe a role for classes of clinically approved drugs and also an unclassified class of antiDENV agents. This review aims to enhance our understanding of novel agents and their cognate targets in furthering innovations in the use of small molecules for dengue drug therapies. (C) 2019 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:431 / 455
页数:25
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