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Leveraging Natural Product-Inspired Antifungals to Investigate the Mechanism of Action of Peniciaculin A
被引:0
|作者:
Wilt, Ingrid K.
[1
]
Demeritte, Adrian R.
[1
]
Kim, Alexander T.
[1
]
Wang, Weiwei
[2
]
Wuest, William M.
[1
]
机构:
[1] Emory Univ, Dept Chem, 1515 Dickey Dr, Atlanta, GA 30322 USA
[2] Corteva Agrisci, 9330 Zionsville Rd, Indianapolis, IN 46268 USA
来源:
基金:
美国国家科学基金会;
关键词:
Antifungal;
Natural product;
Simplified analogue;
Agriculture;
Quinone outside inhibitor;
RESISTANCE;
STROBILURIN;
D O I:
10.1002/cmdc.202400500
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Ubiquinone mimics known as quinone outside inhibitors (QoIs) are one of the most prominent fungicides used to protect crops in the agricultural industry. Due to chemotype similarities with known QoIs, peniciaculin A, a triaryl natural product, was proposed to exhibit similar broad spectrum antifungal activity against phytopathogens. Instability of the tertiary alcohol and phenol motif, however, prompted exploration of the antifungal properties of simplified analogues to probe possible overlap in mechanism of action between the natural product and QoIs. Peniciaculin A inspired analogues mimicking known QoI scaffolds displayed broad spectrum antifungal activity while those containing scaffolds dissimilar to QoIs possessed negligible bioactivity. These activity profiles suggest peniciaculin A is likely acting as a QoI.
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页数:11
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