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Pyrazolo[3,4-d]pyrimidin-4-one derivatives bearing an aniline group: design, synthesis and antifungal activity

Xiaobin Wang, Huajian Chen, Lili Yan, Nan Zhang, Ruiying Wang, Ying Xu, Jiaying Zhu, and Juan Zhang

Research Center of Ocean Engineering Technology, Jiangsu Key Laboratory of Marine Pharmaceutical Compound Screening, Jiangsu Ocean University, Lianyungang, China

 

E-mail: j_zhang@jou.edu.cn

Received: 9 October 2024  Accepted: 18 February 2025

Abstract:

Detecting novel agricultural fungicides has be regarded as the important safeguard for maintaining the development of sustainable agriculture. Aiming to develop novel candidates of agricultural fungicides, the 3-(phenylamino)quinazolin-4(3H)-one emerging as a known antifungal skeleton was modified by assimilating a pyrazole fragment to construct nineteen novel pyrazolo[3,4-d]pyrimidin-4-one derivatives bearing an aniline group. After structural confirmations, the obtained pyrazolo[3,4-d]pyrimidin-4-one derivatives were evaluated for their antifungal activities against Fusarium graminearum, Rhizoctonia solani, Botrytis cinerea and Alternaria solani. The above antifungal bioassays indicated that some pyrazolo[3,4-d]pyrimidin-4-one derivatives bearing a bulky electronegative unit at the ortho-position of an aniline scaffold could exhibit the conspicuous antifungal effect against F. graminearum. Among them, the anti-F. graminearum EC50 value of a target compound 5m was measured as 5.61 μg/mL, which is distinctly superior to that of hymexazol (56.19 μg/mL). The above results provided a necessary replenishment for discovering novel antifungal leads owing the development prospect on effectively controlling Fusarium head blight.

Graphical abstract

Keywords: Lead discovery; Pyrazolo[3,4-d]pyrimidin-4-one; Anfungal activity; Fusarium graminearum

Full paper is available at www.springerlink.com.

DOI: 10.1007/s11696-025-03973-1

 

Chemical Papers 79 (5) 2873–2882 (2025)

Monday, May 19, 2025

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