Design and synthesis of novel 2,2-dimethylchromene derivatives as potential antifungal agents

被引:9
作者
Li, Yong [1 ]
Luo, Bilan [1 ]
Luo, Zhongfu [1 ]
Ma, Taigui [1 ]
Fan, Lingling [1 ]
Liu, Wenjing [1 ]
Fan, Judi [1 ]
Guo, Bing [1 ]
Xue, Wei [2 ]
Tang, Lei [1 ]
机构
[1] Guizhou Med Univ, Coll Pharm,Guizhou Prov Key Lab Pathogenesis & Dr, Guizhou Prov Engn Technol Res Ctr Chem Drug R&D G, Sch Basic Med Sci,State Key Lab Funct & Applicat, Guiyang 550004, Peoples R China
[2] Guizhou Univ, Key Lab Green Pesticide & Agr Bioengn, Minist Educ, Guiyang 550025, Peoples R China
基金
中国国家自然科学基金;
关键词
2,2-dimethylchromene; Synthesis; Antifungal activity; Structure-activity relationships; PRECOCENE-I; CHROMENES; GLABRIDIN;
D O I
10.1007/s11030-022-10421-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In order to find novel environment-friendly and effective antifungal agents, four series of 2,2-dimethyl-2H-chromene derivatives were designed, synthesized and characterized by spectroscopic analysis. The antifungal activities of all the target compounds against nine phytopathogenic fungi were evaluated in vitro. Preliminary results indicated that most of the target compounds exhibited obvious antifungal activity at the concentration of 50 mu g/mL. Among them, compound 4j displayed more promising antifungal potency against Fusarium solani, Pyricularia oryzae, Alternaria brassicae, Valsa mali and Alternaria alternata strains than the two commercially available fungicides chlorothalonil and hymexazol, with the corresponding EC50 values of 6.3, 7.7, 7.1, 7.5, 4.0 mu g/mL, respectively. Moreover, the cell experiments results suggested that the target compounds had low cytotoxicity to the PC12 cell. This research will provide theoretical basis for the future application of 2,2-dimethyl-2H-chromenes as botanical fungicides in agriculture. [GRAPHICS] .
引用
收藏
页码:589 / 601
页数:13
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