化学
拟肽
登革热病毒
蛋白质-蛋白质相互作用
小分子
抗病毒药物
病毒学
药物发现
药物开发
计算生物学
登革热
基孔肯雅
药品
病毒
生物化学
生物
药理学
肽
作者
Violeta Marković,Anna Szczepańska,Łukasz Berlicki
标识
DOI:10.1021/acs.jmedchem.3c01543
摘要
Continually repeating outbreaks of pathogenic viruses necessitate the construction of effective antiviral strategies. Therefore, the development of new specific antiviral drugs in a well-established and efficient manner is crucial. Taking into account the strong ability of viruses to change, therapies with diversified molecular targets must be sought. In addition to the widely explored viral enzyme inhibitor approach, inhibition of protein-protein interactions is a very valuable strategy. In this Perspective, protein-protein interaction inhibitors targeting HIV, SARS-CoV-2, HCV, Ebola, Dengue, and Chikungunya viruses are reviewed and discussed. Antibodies, peptides/peptidomimetics, and small molecules constitute three classes of compounds that have been explored, and each of them has some advantages and disadvantages for drug development.
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