Evaluation of antifungal activities and structure-activity relationships of coumarin derivatives

被引:63
作者
Song, Ping-Ping [1 ,2 ,3 ]
Zhao, Jun [1 ]
Liu, Zong-Liang [4 ]
Duan, Ya-Bing [1 ]
Hou, Yi-Ping [1 ]
Zhao, Chun-Qing [1 ]
Wu, Min [1 ]
Wei, Min [2 ,3 ]
Wang, Nian-He [2 ,3 ]
Lv, Ye [2 ,3 ]
Han, Zhao-Jun [1 ]
机构
[1] Nanjing Agr Univ, Coll Plant Protect, Key Lab Monitoring & Management Crop Dis & Pest I, Minist Agr, Nanjing 210095, Jiangsu, Peoples R China
[2] Jiangsu Ctr Res & Dev Med Plants, Inst Bot, Nanjing, Jiangsu, Peoples R China
[3] Chinese Acad Sci, Nanjing, Jiangsu, Peoples R China
[4] Yantai Univ, Key Lab Mol Pharmacol & Drug Evaluat, Sch Pharm,Minist Educ, Collaborat Innovat Ctr Adv Drug Delivery Syst & B, Yantai, Shandong, Peoples R China
关键词
natural coumarins; linear pyranocoumarin; angular pyranocoumarin; antifungal activity; structure-activity relationships; IN-VITRO; OSTHOL; FUNGICIDES;
D O I
10.1002/ps.4422
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
BACKGROUNDOsthol is a natural coumarin and lead compound that has been developed into commercial fungicides in China. Natural coumarins comprise five major subtypes: simple coumarins, linear furanocoumarins, angular furanocoumarins, linear pyranocoumarins and angular pyranocoumarins. Studies pertaining to the antifungal activities of linear pyranocoumarins are few, and no reports exist for the antifungal activities of angular pyranocoumarins. In order to discover more antifungal natural coumarins, we synthesised a series of simple natural coumarins and isolated several plant-based furanocoumarins and pyranocoumarins using previously described methods. The compounds were biologically evaluated against some plant fungal pathogens. RESULTSSeveral of the 35 coumarins evaluated here exhibited strong activities against specific fungal species, including compound 25 (Pd-D-V, a linear pyranocoumarin), compound 26 (libanorin, an angular furanocoumarin) and compound 34 (disenecioyl khellactone, an angular pyranocoumarin). Compound 25 exhibited a high activity against Sclerotinia sclerotiorum (EC50 = 13.2 mu g mL(-1)); compound 34 displayed a strong antifungal activity against Botrytis cinerea (EC50 = 11.0 mu g mL(-1)). CONCLUSIONThis study demonstrates that several natural coumarins (one linear pyranocoumarin and one angular pyranocoumarin in particular) exhibit strong antifungal activities. These results call for further studies, where these coumarins can be examined as potential lead compounds for developing novel antifungal agents. (c) 2016 Society of Chemical Industry
引用
收藏
页码:94 / 101
页数:8
相关论文
共 35 条
[1]  
BABA K, 1985, Shoyakugaku Zasshi, V39, P282
[2]   Synthesis and antifungal activity of novel 7-O-substituted pyridyl-4-methyl coumarin derivatives [J].
Chai, Xiaoyun ;
Yu, Shichong ;
Wang, Xiaoyan ;
Wang, Nan ;
Zhu, Zhanzhou ;
Zhang, Dazhi ;
Wu, Qiuye ;
Cao, Yongbing ;
Sun, Qingyan .
MEDICINAL CHEMISTRY RESEARCH, 2013, 22 (10) :4654-4662
[3]   Activity of the novel fungicide SYP-Z048 against plant pathogens [J].
Chen, Fengping ;
Han, Ping ;
Liu, Pengfei ;
Si, Naiguo ;
Liu, Junli ;
Liu, Xili .
SCIENTIFIC REPORTS, 2014, 4
[4]  
Chen H, 2010, CHINESE AGR SCI B, V26, P26
[5]   Synthesis and antifungal evaluation of a series of maleimides [J].
Chen, Xiao-Long ;
Zhang, Li-Jun ;
Li, Fu-Ge ;
Fan, Yong-Xian ;
Wang, Wei-Ping ;
Li, Bao-Ju ;
Shen, Yin-Chu .
PEST MANAGEMENT SCIENCE, 2015, 71 (03) :433-440
[6]   Screening study for potential lead compounds for natural product-based fungicides:: I.: Synthesis and in vitro evaluation of coumarins against Botrytis cinerea [J].
Daoubi, M ;
Durán-Patrón, RD ;
Hmamouchi, M ;
Hernández-Galán, R ;
Benharref, A ;
Collado, IG .
PEST MANAGEMENT SCIENCE, 2004, 60 (09) :927-932
[7]   Synthesis, Structure-Activity Relationships (SAR) and in Silico Studies of Coumarin Derivatives with Antifungal Activity [J].
de Araujo, Rodrigo S. A. ;
Guerra, Felipe Q. S. ;
Lima, Edeltrudes de O. ;
de Simone, Carlos A. ;
Tavares, Josean F. ;
Scotti, Luciana ;
Scotti, Marcus T. ;
de Aquino, Thiago M. ;
de Moura, Ricardo O. ;
Mendonca, Francisco J. B., Jr. ;
Barbosa-Filho, Jose M. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (01) :1293-1309
[8]   Design, synthesis and structure-activity relationship of novel coumarin derivatives [J].
Guan, Ai-Ying ;
Liu, Chang-Ling ;
Li, Miao ;
Zhang, Hong ;
Li, Zhi-Nian ;
Li, Zheng-Ming .
PEST MANAGEMENT SCIENCE, 2011, 67 (06) :647-655
[9]   Identification and structure-activity relationship studies of osthol, a cytotoxic principle from Cnidium monnieri [J].
Hitotsuyanagi, Y ;
Kojima, H ;
Ikuta, H ;
Takeya, K ;
Itokawa, H .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1996, 6 (15) :1791-1794
[10]   Pharmacological and biochemical actions of simple coumarins: Natural products with therapeutic potential [J].
Hoult, JRS ;
Paya, M .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1996, 27 (04) :713-722