抗疟药
部分
疟疾
化学
药理学
恶性疟原虫
耐受性
药品
组合化学
医学
立体化学
不利影响
免疫学
作者
Lekkala Ravindar,Siti Aishah Hasbullah,K.P. Rakesh,Nurul Izzaty Hassan
标识
DOI:10.1016/j.ejmech.2023.115458
摘要
Malaria is the fifth most lethal parasitic infection in the world. Antimalarial medications have played a crucial role in preventing and eradicating malaria. Numerous heterocyclic moieties have been incorporated into the creation of effective antimalarial drugs. The 4-aminoquinoline moiety is favoured in antimalarial drug discovery due to the diverse biological applications of its derivative. Since the 1960s, 4-aminoquinoline has been an important antimalarial drug due to its low toxicity, high tolerability, and rapid absorption after administration. This review focused on the antimalarial efficacy of the 4-aminoquinoline moiety hybridised with various heterocyclic scaffolds developed by scientists since 2018 against diverse Plasmodium clones. It could aid in the future development of more effective antimalarial agents.
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