氯喹诺尔
体内
氟康唑
白色念珠菌
化学
药理学
体外
白色体
细胞毒性
抗真菌
微生物学
生物化学
医学
生物
生物技术
作者
Liping Li,Hao Wu,Jiayin Wang,Zhe Ji,Ting Fang,Hui Lu,Lan Yan,Fu‐Ming Shen,Dazhi Zhang,Yuanying Jiang,Tingjunhong Ni
标识
DOI:10.1021/acs.jmedchem.3c01771
摘要
Fungal pathogens can cause life-threatening infections, yet current antifungals are inadequate at treating many of these, highlighting the importance of novel drug discovery. Here, we report hit compound L14, a novel 8-hydroxyquinoline derivative with potent and broad-spectrum antifungal activity. In vitro experiments exhibited that L14 had better activity and lower cytotoxicity than that of clioquinol and showed synergy in combination with fluconazole (FLC). In a Candida albicans-infected murine model, L14 at 2 mg/kg showed better in vivo efficacy than clioquinol at reducing fungal burden and extending the survival of C. albicans-infected mice. In addition, L14 alone or in combination with FLC had significant inhibitory activity against hypha and biofilm formation. Overall, our data indicated that 8-hydroxyquinoline derivative L14 has favorable pharmacokinetics and acceptable safety profiles and could be further investigated as a promising antifungal hit compound.
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