抗真菌
抗真菌药
化学
微生物学
杀菌剂
体内
离体
药品
最小抑制浓度
抗药性
药理学
生物
体外
生物化学
生物技术
植物
作者
Ji‐Won Choi,Kyung‐Tae Lee,Siwon Kim,Ye Rim Lee,Hyeon Ji Kim,Kyung Jin Seo,Myung Ha Lee,Seul Ki Yeon,Bo Ko Jang,Sun Jun Park,Hyeon Jeong Kim,Jong‐Hyun Park,Dahee Kim,Dong‐Gi Lee,Eunji Cheong,Jong-Seung Lee,Yong‐Sun Bahn,Ki Duk Park
标识
DOI:10.1021/acs.jmedchem.1c01299
摘要
Due to the increased morbidity and mortality by fungal infections and the emergence of severe antifungal resistance, there is an urgent need for new antifungal agents. Here, we screened for antifungal activity in our in-house library through the minimum inhibitory concentration test and derived two hit compounds with moderate antifungal activities. The hit compounds' antifungal activities and drug-like properties were optimized by substituting various aryl ring, alkyl chain, and methyl groups. Among the optimized compounds, 22h was the most promising candidate with good drug-like properties and exhibited potent fast-acting fungicidal antifungal effects against various fungal pathogens and synergistic antifungal activities with some known antifungal drugs. Additionally, 22h was further confirmed to disturb fungal cell wall integrity by activating multiple cell wall integrity pathways. Furthermore, 22h exerted significant antifungal efficacy in both the subcutaneous infection mouse model and ex vivo human nail infection model.
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