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吡噁唑菌酮类似物的合成及杀菌活性

白慧 刘彦斐 傅滨 肖玉梅 覃兆海

高等学校化学学报2026,Vol.47Issue(7):91-103,13.
高等学校化学学报2026,Vol.47Issue(7):91-103,13.DOI:10.7503/cjcu20260128

吡噁唑菌酮类似物的合成及杀菌活性

Synthesis and Fungicidal Activity of Pyramoxadone Analogues

白慧 1刘彦斐 2傅滨 2肖玉梅 2覃兆海2

作者信息

  • 1. 石家庄信息工程职业学院生物医药技术系,石家庄 052161
  • 2. 中国农业大学理学院,北京 100193
  • 折叠

摘要

Abstract

A series of novel oxazolidinedione derivatives(2-2-2-30)was designed and synthesized based on the structure of pyramoxadone,a 5-position pyridine analogue of famoxadone.The target compounds were characterized by means of 1H NMR,13C NMR and high-resolution mass spectrometry(HRMS).Their in vitro antifungal activities were evaluated against nine plant pathogenic fungi using the mycelial growth rate method,with famoxadone as a positive control.Preliminary screening at 50 mg/L revealed that most compounds exhibited moderate to excellent inhibitory activity,particularly against Rhizoctonia solani,Sclerotinia sclerotiorum,Botrytis cinerea,and Pyricularia grisea.Structure-activity relationship(SAR)analysis indicated that bulky groups such as tert-butyl and cyclohexyl are detrimental to the enhancement of antifungal activity,while fluorine-containing compounds generally exhibited en-hanced antifungal activity.Compounds 2-16(EC50=3.78 mg/L)and 2-26(EC50=1.61 mg/L)exhibited superior activity against R.solani compared to famoxadone(EC50=4.38 mg/L)and pyramoxadone(EC50=9.67 mg/L).In vivo protective efficacy assays demonstrated that compounds 2-13,2-16 and 2-18 provided 88.3%,89.5%and 81.7%control against cotton damping-off at 200 mg/L,respectively,significantly outperforming the positive control.Molecular docking and electrostatic surface map analysis revealed that the SAR of this class of compounds follows a pattern where the hydro-phobic skeleton determines the binding orientation,electrostatic complementarity determines the binding strength,and substituent fine-tuning determines the activity level.

关键词

噁唑菌酮/噁唑烷二酮/抑菌活性/构效关系/分子对接

Key words

Famoxadone/Oxazolidinedione/Antifungal activity/Structure-activity relationship(SAR)/Molecular docking

分类

化学化工

引用本文复制引用

白慧,刘彦斐,傅滨,肖玉梅,覃兆海..吡噁唑菌酮类似物的合成及杀菌活性[J].高等学校化学学报,2026,47(7):91-103,13.

基金项目

国家自然科学基金(批准号:21877125)资助. Supported by the National Natural Science Foundation of China(No.21877125). (批准号:21877125)

高等学校化学学报

0251-0790

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