Novel Dioxolane Ring Compounds for the Management of Phytopathogen Diseases as Ergosterol Biosynthesis Inhibitors :Synthesis, Biological Activities, and Molecular Docking

被引:34
作者
Min, Li-Jing [1 ]
Wang, Han [2 ]
Bajsa-Hirschel, Joanna [3 ]
Yu, Chen-Sheng [2 ]
Wang, Bin [2 ,4 ]
Yao, Meng-Meng [2 ,4 ]
Han, Liang [2 ]
Cantrell, Charles L. [3 ]
Duke, Stephen O. [5 ]
Sun, Na-Bo [4 ]
Liu, Xing-Hai [2 ]
机构
[1] Huzhou Univ, Coll Life Sci, Key Lab Vector Biol & Pathogen Control Zhejiang P, Huzhou 313000, Zhejiang, Peoples R China
[2] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310014, Peoples R China
[3] USDA ARS, Nat Prod Utilizat Res Unit, University, MS 38677 USA
[4] Zhejiang Shuren Univ, Coll Biol & Environm Engn, Hangzhou 310015, Zhejiang, Peoples R China
[5] Univ Mississippi, Sch Pharm, Natl Ctr Nat Prod Res, University, MS 38677 USA
关键词
ergosterol biosynthesis inhibitor; dioxolane ring compounds; SAR; mode of action; brassinosteroid; CRYSTAL-STRUCTURE; GROWTH;
D O I
10.1021/acs.jafc.2c00541
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Thirty novel dioxolane ring compounds were designed and synthesized. Their chemical structures were confirmed by1H NMR, HRMS, and single crystal X-ray diffraction analysis. Bioassays indicated that these dioxolane ring derivatives exhibitedexcellent fungicidal activity againstRhizoctonia solani,Pyricularia oryae,Botrytis cinerea,Colletotrichum gloeosporioides,Fusariumoxysporum,Physalospora piricola,Cercospora arachidicolaand herbicidal activity against lettuce (Lactuca sativa), bentgrass (Agrostisstolonifera), and duckweed (Lemna pausicostata). Among these compounds, 1-((2-(4-chlorophenyl)-5-methyl-1,3-dioxan-2-yl)methyl)-1H-1,2,4-triazole (D17), 1-(((4R)-2-(4-chlorophenyl)-4-methyl-1,3-dioxolan-2-yl)methyl)-1H-1,2,4-triazole (D20), 1-((5-methyl-2-(4-(trifluoromethyl)phenyl)-1,3-dioxan-2-yl)methyl)-1H-1,2,4-triazole (D22), and 1-((2-(4-fluorophenyl)-1,3-dioxo-lan-2-yl)methyl)-1H-1,2,4-triazole (D26) had broad spectrum fungicidal and herbicidal activity. The IC50values against duckweedwere 20.5 +/- 9.0, 14.2 +/- 6.7, 24.0 +/- 11.0, 8.7 +/- 3.5, and 8.0 +/- 3.1 mu M forD17,D20,D22, andD26and the positive controldifenoconazole, respectively. The EC50values were 7.31 +/- 0.67, 9.74 +/- 0.83, 17.32 +/- 1.23, 11.96 +/- 0.98, and 8.93 +/- 0.91 mg/L forD17,D20,D22, andD26and the positive control difenoconazole against the plant pathogenR. solani, respectively. Germinationexperiments withArabidopsisseeds indicated that the target of these dioxolane ring compounds in plants is brassinosteroidbiosynthesis. Molecular simulation docking results of compoundD26and difenoconazole with fungal CYP51 P450 confirmed thatthey both inhibit this enzyme involved in ergosterol biosynthesis. The structure-activity relationships (SAR) are discussed bysubstituent effect, molecular docking, and density functional theory analysis, which provided useful information for designing moreactive compounds
引用
收藏
页码:4303 / 4315
页数:13
相关论文
共 50 条
[1]   Triadimefon, a fungicidal triazole-type P450 inhibitor, induces brassinosteroid deficiency-like phenotypes in plants and binds to DWF4 protein in the brassinosteroid biosynthesis pathway [J].
Asami, T ;
Mizutani, M ;
Shimada, Y ;
Goda, H ;
Kitahata, N ;
Sekimata, K ;
Han, SY ;
Fujioka, S ;
Takatsuto, S ;
Sakata, K ;
Yoshida, S .
BIOCHEMICAL JOURNAL, 2003, 369 (01) :71-76
[2]   Characterization of brassinazole, a triazole-type brassinosteroid biosynthesis inhibitor [J].
Asami, T ;
Min, YK ;
Nagata, N ;
Yamagishi, K ;
Takatsuto, S ;
Fujioka, S ;
Murofushi, N ;
Yamaguchi, I ;
Yoshida, S .
PLANT PHYSIOLOGY, 2000, 123 (01) :93-99
[3]   Synthesis and Biological Evaluation of Some New N1-[4-(4-Chlorophenylsulfonyl)benzoyl]-N4-(aryl)-thiosemicarbazides and Products of Their Cyclization [J].
Barbuceanu, Stefania-Felicia ;
Bancescu, Gabriela ;
Saramet, Gabriel ;
Barbuceanu, Florica ;
Draghici, Constantin ;
Radulescu, Flavian Stefan ;
Ionescu, Aura ;
Negres, Simona .
HETEROATOM CHEMISTRY, 2013, 24 (04) :309-321
[4]   The SWISS-MODEL Repository-new features and functionality [J].
Bienert, Stefan ;
Waterhouse, Andrew ;
de Beer, Tjaart A. P. ;
Tauriello, Gerardo ;
Studer, Gabriel ;
Bordoli, Lorenza ;
Schwede, Torsten .
NUCLEIC ACIDS RESEARCH, 2017, 45 (D1) :D313-D319
[5]   Update on mechanisms of azole resistance in Mycosphaerella graminicola and implications for future control [J].
Cools, Hans J. ;
Fraaije, Bart A. .
PEST MANAGEMENT SCIENCE, 2013, 69 (02) :150-155
[6]   Cross-resistance between myclobutanil and tebuconazole and the genetic basis of tebuconazole resistance inVenturia inaequalis [J].
Cordero-Limon, Laura ;
Shaw, Michael W. ;
Passey, Thomas A. J. ;
Robinson, Joyce D. ;
Xu, Xiangming .
PEST MANAGEMENT SCIENCE, 2021, 77 (02) :844-850
[7]   Investigating the mode of action of natural phytotoxins [J].
Dayan, FE ;
Romagni, JG ;
Duke, SO .
JOURNAL OF CHEMICAL ECOLOGY, 2000, 26 (09) :2079-2094
[8]  
Desta B., CHEM BIOL TECHNOL AG, V2021, P1
[9]  
Ding Q. C., 2021, CHINESE J STRUC CHEM, V40, P1531
[10]  
Ding QC, 2021, CHINESE J STRUC CHEM, V40, P1098, DOI 10.14102/j.cnki.0254-5861.2011-3225