Antiviral activity of cationic amphiphilic drugs

被引:97
作者
Salata, Cristiano [1 ]
Calistri, Arianna [1 ]
Parolin, Cristina [1 ]
Baritussio, Aldo [2 ]
Palu, Giorgio [1 ]
机构
[1] Univ Padua, Dept Mol Med, Via Aristide Gabelli 63, I-35121 Padua, Italy
[2] Univ Padua, Dept Med, Clin Med 1, Padua, Italy
关键词
Amiodarone; antivirals; cationic amphiphilic drugs; chloroquine; chikungunya virus; Crimean-Congo hemorrhagic fever virus; dengue virus; ebola virus; emerging viruses; enterovirus; hepatitis C virus; Herpes simplex virus; ion channel blockers; protein kinase inhibitors; psychoactive drug; selective estrogen receptor modulators; U18666A; Zika virus; CHOLESTEROL TRANSPORT INHIBITOR; SMALL-MOLECULE INHIBITORS; C VIRUS-INFECTION; EBOLA-VIRUS; DENGUE VIRUS; MEDIATED ENDOCYTOSIS; VIRAL-INFECTIONS; LATE ENDOSOMES; CHLOROQUINE; AMIODARONE;
D O I
10.1080/14787210.2017.1305888
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: Emerging and reemerging viral infections represent a major concern for human and veterinary public health and there is an urgent need for the development of broad-spectrum antivirals.Areas covered: A recent strategy in antiviral research is based on the identification of molecules targeting host functions required for infection of multiple viruses. A number of FDA-approved drugs used to treat several human diseases are cationic amphiphilic drugs (CADs) that have the ability to accumulate inside cells affecting several structures/functions hijacked by viruses during infection. In this review we summarized the CADs' chemical properties and effects on the cells and reported the main FDA-approved CADs that have been identified so far as potential antivirals in drug repurposing studies.Expert commentary: Although there have been concerns regarding the efficacy and the possible side effects of the off-label use of CADs as antivirals, they seem to represent a promising starting point for the development of broad-spectrum antiviral strategies. Further knowledge about their mechanism of action is required to improve their antiviral activity and to reduce the risk of side effects.
引用
收藏
页码:483 / 492
页数:10
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