可药性
药物发现
表型筛选
疟疾
生物信息学
计算生物学
抗疟药
疟原虫(生命周期)
生物
药品
恶性疟原虫
生物信息学
计算机科学
药理学
表型
遗传学
寄生虫寄主
免疫学
万维网
基因
作者
Nik Nur Solehah Fitri Nik Mohd Azam,Shatrah Othman,Yeun‐Mun Choo
标识
DOI:10.2174/0109298673312727240527064833
摘要
Malaria remains a significant global health threat despite extensive efforts aimed at its eradication. Numerous challenges persist in eliminating the disease, chief among them being the parasite's ability to mutate, resulting in drug resistance. The discovery of antimalarial drugs has relied on both phenotypic and target-based approaches. While phenotypic screening has identified promising candidates, target-based methods offer a more precise approach by leveraging chemically validated targets and computational tools. Analysis of Plasmodium spp. protein structures reveal druggable targets, offering opportunities for in silico screening. Combining compounds from natural and synthetic sources in a target-based approach accelerates the discovery of new antimalarial agents. This review explores previous breakthroughs in antimalarial drug discovery from natural products and synthetic origins, emphasizing their specific target proteins within Plasmodium species.
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