抗真菌
抗真菌药
药理学
药代动力学
计算生物学
医学
疟疾
人类健康
化学
伊曲康唑
生物
真菌病原
药物发现
真菌生长
念珠菌感染
侵袭性念珠菌病
代谢活性
抗真菌药
两性霉素B
恶性疟原虫
人类病原体
抗疟药
作者
Amrendra Kumar,Ju-Hsin Chia,Kevin A. Reynolds,Jane X. Kelly,Papireddy Kancharla
标识
DOI:10.1021/acsmedchemlett.5c00656
摘要
Human fungal infections pose a major global health challenge, underscoring the urgent need for new chemotypes that are effective against multidrug-resistant (MDR) fungal pathogens such as Candida auris . Tambjamines (TAs), previously characterized for their potent antimalarial and antileishmanial activities, were investigated for their antifungal potential. A selected series of TA analogs exhibited excellent in vitro activity against C. albicans and C. auris at low micromolar concentrations. Among them, the antimalarial lead TA, KAR1123 ( 15 ), exhibited marked antifungal activity against both strains, with superior inhibition of C. auris, while displaying favorable cytotoxicity, metabolic stability, and pharmacokinetic properties. Structure–activity relationship analyses highlighted key structural elements required for antifungal potency. Collectively, this study represents the first evidence of TA activity against C. auris and establishes a promising foundation for the development of next-generation antifungal agents targeting MDR fungal pathogens.
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