Marwa Almulhim, Abdolmajid Ghasemian, Mojtaba Memariani, Farnaz Karami, Asmaa S A Yassen, Athanasios Alexiou, Marios Papadakis, Gaber El-Saber Batiha
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A comprehensive literature search was performed to identify existing studies, clinical trials, and reviews that discuss drug repositioning strategies for the treatment of emerging and re-emerging viral infections using databases, such as PubMed, Scholar Google, Scopus, and Web of Science. By utilizing drug repositioning, pharmaceutical companies can take advantage of a cost-effective, accelerated, and effective strategy, which in turn leads to the discovery of innovative treatment options for patients. In light of antiviral drug resistance and the high costs of developing novel antivirals, drug repositioning holds great promise for more rapid substitution of approved drugs. Main repositioned drugs have included chloroquine, ivermectin, dexamethasone, Baricitinib, tocilizumab, Mab114 (Ebanga™), ZMapp (pharming), Artesunate, imiquimod, saquinavir, capmatinib, naldemedine, Trametinib, statins, celecoxib, naproxen, metformin, ruxolitinib, nitazoxanide, gemcitabine, Dorzolamide, Midodrine, Diltiazem, zinc acetate, suramin, 5-fluorouracil, quinine, minocycline, trifluoperazine, paracetamol, berbamine, Nifedipine, and chlorpromazine. 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引用次数: 0
摘要
在流行病和大流行期间新出现和再出现的病毒病原体的全球影响导致严重的健康和经济负担。新出现或再出现的主要病毒包括SARS-CoV-2、埃博拉病毒(EBOV)、猴痘病毒(Mpox)、肝炎病毒、寨卡病毒、禽流感、流感病毒、基孔肯雅病毒(CHIKV)、登革热病毒(DENV)、西尼罗河病毒、横纹肌病毒、白蛉热病毒、克里米亚-刚果出血热病毒和裂谷热病毒(RVFV)。利用PubMed、Scholar b谷歌、Scopus和Web of Science等数据库,进行全面的文献检索,以确定现有的研究、临床试验和综述,讨论治疗新发和再发病毒感染的药物重新定位策略。通过利用药物重新定位,制药公司可以利用成本效益,加速和有效的策略,从而为患者发现创新的治疗方案。鉴于抗病毒药物的耐药性和开发新型抗病毒药物的高成本,药物重新定位有望更快地替代已批准的药物。重新定位的主要药物有:氯喹、伊维菌素、地塞米松、Baricitinib、tocilizumab、Mab114 (Ebanga™)、ZMapp (pharming)、青蒿琥酯、咪喹莫德、沙奎那韦、卡马替尼、纳尔美定、曲美替尼、他汀类药物、塞来昔布、萘普生、二甲双胍、鲁索利替尼、硝唑尼、吉西他滨、Dorzolamide、Midodrine、地尔硫卓、醋酸锌、苏拉明、5-氟尿嘧啶、奎宁、米诺环素、三氟哌嗪、对乙酰氨基酚、小檗碱、硝苯地平、氯丙嗪。这篇简短的综述将深入研究重新定位的药物,这些药物已被用于对抗新出现和再出现的病毒病原体。
Drug repositioning as a promising approach for the eradication of emerging and re-emerging viral agents.
The global impact of emerging and re-emerging viral agents during epidemics and pandemics leads to serious health and economic burdens. Among the major emerging or re-emerging viruses include SARS-CoV-2, Ebola virus (EBOV), Monkeypox virus (Mpox), Hepatitis viruses, Zika virus, Avian flu, Influenza virus, Chikungunya virus (CHIKV), Dengue fever virus (DENV), West Nile virus, Rhabdovirus, Sandfly fever virus, Crimean-Congo hemorrhagic fever (CCHF) virus, and Rift Valley fever virus (RVFV). A comprehensive literature search was performed to identify existing studies, clinical trials, and reviews that discuss drug repositioning strategies for the treatment of emerging and re-emerging viral infections using databases, such as PubMed, Scholar Google, Scopus, and Web of Science. By utilizing drug repositioning, pharmaceutical companies can take advantage of a cost-effective, accelerated, and effective strategy, which in turn leads to the discovery of innovative treatment options for patients. In light of antiviral drug resistance and the high costs of developing novel antivirals, drug repositioning holds great promise for more rapid substitution of approved drugs. Main repositioned drugs have included chloroquine, ivermectin, dexamethasone, Baricitinib, tocilizumab, Mab114 (Ebanga™), ZMapp (pharming), Artesunate, imiquimod, saquinavir, capmatinib, naldemedine, Trametinib, statins, celecoxib, naproxen, metformin, ruxolitinib, nitazoxanide, gemcitabine, Dorzolamide, Midodrine, Diltiazem, zinc acetate, suramin, 5-fluorouracil, quinine, minocycline, trifluoperazine, paracetamol, berbamine, Nifedipine, and chlorpromazine. This succinct review will delve into the topic of repositioned drugs that have been utilized to combat emerging and re-emerging viral pathogens.
期刊介绍:
Molecular Diversity is a new publication forum for the rapid publication of refereed papers dedicated to describing the development, application and theory of molecular diversity and combinatorial chemistry in basic and applied research and drug discovery. The journal publishes both short and full papers, perspectives, news and reviews dealing with all aspects of the generation of molecular diversity, application of diversity for screening against alternative targets of all types (biological, biophysical, technological), analysis of results obtained and their application in various scientific disciplines/approaches including:
combinatorial chemistry and parallel synthesis;
small molecule libraries;
microwave synthesis;
flow synthesis;
fluorous synthesis;
diversity oriented synthesis (DOS);
nanoreactors;
click chemistry;
multiplex technologies;
fragment- and ligand-based design;
structure/function/SAR;
computational chemistry and molecular design;
chemoinformatics;
screening techniques and screening interfaces;
analytical and purification methods;
robotics, automation and miniaturization;
targeted libraries;
display libraries;
peptides and peptoids;
proteins;
oligonucleotides;
carbohydrates;
natural diversity;
new methods of library formulation and deconvolution;
directed evolution, origin of life and recombination;
search techniques, landscapes, random chemistry and more;