Oleanane-Type Triterpene Conjugates with 1H-1,2,3-Triazole Possessing of Fungicidal Activity

被引:13
作者
Chen, Zili [1 ]
Jiang, Yu [1 ]
Xu, Chen [1 ]
Sun, Xiangyu [2 ]
Ma, Chao [3 ]
Xia, Zihao [1 ]
Zhao, Hanqing [1 ]
机构
[1] Beijing Univ Agr, Key Lab Northern Urban Agr, Minist Agr & Rural Affairs, Beijing 102206, Peoples R China
[2] Minist Sci & Technol, Torch High Technol Ind Dev Ctr, Beijing 100045, Peoples R China
[3] Beijing Zhong Bao Green Agr Technol Grp Co Ltd, Beijing 100193, Peoples R China
关键词
oleanolic acid; triazoles; fungicides; new pesticides; ACID;
D O I
10.3390/molecules27154928
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
The triazole pesticide is an organic nitrogen-containing heterocyclic compound with a 1,2,3-Triazole ring. In order to develop a potential glucosamine-6-phosphate synthase (GlmS) inhibitor bactericide, 18 triazole-derivative compounds were synthesized efficiently. In addition, these compounds have not been reported in the literature. The structure was confirmed by high-resolution mass spectrometry (HRMS), H-1 NMR and C-13 NMR. The potential use of the most promising derivatives has been investigated by testing their antifungal activity and enzyme inhibitory activity, revealing inhibitory activities in the low micromolar range. Among them, the antifungal effects of compounds 1e, 1f, 1g, 2e, 2f, and 2g on Sclerotinia sclerotiorum were particularly significant, all of which were above 83%. These compounds will be further investigated as potential antifungal lead compounds. Their structure-activity relationships are discussed based on the effects of substituted phenyl groups on compounds.
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页数:13
相关论文
共 30 条
[1]   Synthesis, biological evaluation and molecular modeling of 1,2,3-triazole analogs of combretastatin A-1 [J].
Akselsen, Oyvind W. ;
Odlo, Kristin ;
Cheng, Jing-Jy ;
Maccari, Giorgio ;
Botta, Maurizio ;
Hansen, Trond Vidar .
BIOORGANIC & MEDICINAL CHEMISTRY, 2012, 20 (01) :234-242
[2]   Exploration of click reaction for the synthesis of modified nucleosides as chitin synthase inhibitors [J].
Chaudhary, Preeti M. ;
Chavan, Sayalee R. ;
Shirazi, Fazal ;
Razdan, Meenakshi ;
Nimkar, Prachi ;
Maybhate, Shailaja P. ;
Likhite, Anjali P. ;
Gonnade, Rajesh ;
Hazara, Braja G. ;
Deshpande, Mukund V. ;
Deshpande, Sunita R. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2009, 17 (06) :2433-2440
[3]  
Crouse GD, 1998, CHEMTECH, V28, P36
[4]   Triazole-based monophosphine ligands for palladium-catalyzed cross-coupling reactions of aryl chlorides [J].
Dai, Q ;
Gao, WZ ;
Liu, D ;
Kapes, LM ;
Zhang, XM .
JOURNAL OF ORGANIC CHEMISTRY, 2006, 71 (10) :3928-3934
[5]   New antifungal agents and preparations [J].
De Pauw, BE .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2000, 16 (02) :147-150
[6]  
Halil S., 2020, ORG COMMUN, V13, P114
[7]  
[胡泊洋 Hu Boyang], 2017, [农药学学报, Chinese Journal of Pesticide Science], V19, P679
[8]  
Hua N.Z., 2016, J CHIN AGROCHEM, V9, P36
[9]  
Kwon TH, 2009, B KOREAN CHEM SOC, V30, P119
[10]   Chemical sensors that incorporate click-derived triazoles [J].
Lau, Yu Heng ;
Rutledge, Peter J. ;
Watkinson, Michael ;
Todd, Matthew H. .
CHEMICAL SOCIETY REVIEWS, 2011, 40 (05) :2848-2866