Optimization and Evaluation of Novel Antifungal Agents for the Treatment of Fungal Infection

Authors
Choi, Ji WonLee, Kyung-TaeKim, SiwonLee, Ye RimKim, Hyeon JiSeo, Kyung JinLee, Myung HaYeon, Seul KiJang, Bo KoPark, Sun JunKim, Hyeon JeongPark, Jong-HyunKim, DaheeLee, Dong-GiCheong, EunjiLee, Jong-SeungBahn, Yong-SunPark, Ki Duk
Issue Date
2021-11-11
Publisher
American Chemical Society
Citation
Journal of Medicinal Chemistry, v.64, no.21, pp.15912 - 15935
Abstract
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.
Keywords
CANDIDA-ALBICANS; DISEASES SOCIETY; CALCINEURIN; RESISTANCE; MANAGEMENT; INHIBITORS; INTEGRITY; SYNTHASE; PATHWAY; UPDATE
ISSN
0022-2623
URI
https://pubs.kist.re.kr/handle/201004/116138
DOI
10.1021/acs.jmedchem.1c01299
Appears in Collections:
KIST Article > 2021
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