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

被引:55
|
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 50 条
  • [31] Structure-Activity Relationships of Neuritogenic Gentiside Derivatives
    Luo, Yan
    Sun, Kaiyue
    Li, Lin
    Gao, Lijuan
    Wang, Guangfa
    Qu, Yuan
    Xiang, Lan
    Chen, Ling
    Hu, Yongzhou
    Qi, Jianhua
    CHEMMEDCHEM, 2011, 6 (11) : 1986 - 1989
  • [32] Design, synthesis and structure-activity relationship of novel coumarin derivatives
    Guan, Ai-Ying
    Liu, Chang-Ling
    Li, Miao
    Zhang, Hong
    Li, Zhi-Nian
    Li, Zheng-Ming
    PEST MANAGEMENT SCIENCE, 2011, 67 (06) : 647 - 655
  • [33] Antifungal and insecticidal activities of rhein derivatives: synthesis, characterization and preliminary structure-activity relationship studies
    Zhu, Xiang
    Chen, Shunshun
    Zheng, Yan
    Zhang, Yong
    Hsiang, Tom
    Huang, Rong
    Qi, Jingwei
    Gan, Tian
    Chang, Yue
    Li, Junkai
    NATURAL PRODUCT RESEARCH, 2022, 36 (16) : 4140 - 4146
  • [34] QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS (QSAR) STUDIES OF BISBENZAMIDINES WITH ANTIFUNGAL ACTIVITY
    de Almeida, Vera L.
    Dias Lopes, Julio Cesar
    Oliveira, Sheila Rodrigues
    Donnici, Claudio L.
    Montanari, Carlos A.
    QUIMICA NOVA, 2010, 33 (07): : 1482 - 1489
  • [35] Synthesis, biological evaluation and structure-activity relationships of new phthalazinedione derivatives with vasorelaxant activity
    Munin, Javier
    Quezada, Elias
    Cuinas, Andrea
    Campos-Toimil, Manuel
    Uriarte, Eugenio
    Santana, Lourdes
    Vina, Dolores
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, 82 : 407 - 417
  • [36] Synthesis, pharmacological evaluation, and structure-activity relationships of benzopyran derivatives with potent SERM activity
    Amari, G
    Armani, E
    Ghirardi, S
    Delcanale, M
    Civelli, M
    Caruso, PL
    Galbiati, E
    Lipreri, M
    Rivara, S
    Lodola, A
    Mor, M
    BIOORGANIC & MEDICINAL CHEMISTRY, 2004, 12 (14) : 3763 - 3782
  • [37] Novel benzoylurea derivatives as potential antitumor agents; Synthesis, activities and structure-activity relationships
    Hwang, KJ
    Park, KH
    Lee, CO
    Kim, BT
    ARCHIVES OF PHARMACAL RESEARCH, 2002, 25 (06) : 781 - 785
  • [38] Synthesis and Structure-Activity Relationships of a Series of Aporphine Derivatives with Antiarrhythmic Activities and Acute Toxicity
    Wang, Hui
    Cheng, Xin
    Kong, Shujun
    Yang, Zixian
    Wang, Hongmei
    Huang, Qiuyan
    Li, Jingyu
    Chen, Cheng
    Ma, Yunshu
    MOLECULES, 2016, 21 (12):
  • [39] Synthesis and Biological Activities of Neoechinulin A Derivatives: New Aspects of Structure-Activity Relationships for Neoechinulin A
    Kuramochi, Kouji
    Ohnishi, Kensuke
    Fujieda, Satoshi
    Nakajima, Mitsuhiro
    Saitoh, Yoshihiko
    Watanabe, Nobuo
    Takeuchi, Toshifumi
    Nakazaki, Atsuo
    Sugawara, Fumio
    Arai, Takao
    Kobayashi, Susumu
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2008, 56 (12) : 1738 - 1743
  • [40] Novel benzoylurea derivatives as potential antitumor agents; synthesis, activities and structure-activity relationships
    Ki -Jun Hwang
    Kyung -Ho Park
    Chong -Ock Lee
    Beom -Tae Kim
    Archives of Pharmacal Research, 2002, 25 : 781 - 785