兰州大学机构库 >药学院
Design, Synthesis, and Antimicrobial Activity of Quindoline Derivatives Inspired by the Cryptolepine Alkaloid
Chu, Qing-Ru1; He, Ying-Hui1; Tang, Chen1; Zhang, ZJ(张智军)1; Luo, Xiong-Fei1; Zhang, Bao-Qi1; Zhou, Yong1; Wu, Tian-Lin1; Du, Sha-Sha1; Yang, Cheng-Jie1; Liu, YQ(刘映前)1,2
2022-03-09
Source PublicationJOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY   Impact Factor & Quartile
ISSN0021-8561
Volume70Issue:9Pages:2851-2863
AbstractBased on the structural characteristics of the cryptolepine alkaloid, a series of new quindoline derivatives bearing various substituents were prepared and evaluated for their fungicidal and antibacterial activities. Bioassay results showed that compound D7 displayed superior in vitro fungicidal activities against Sclerotinia sclerotiorum, Botrytis cinerea, Fusarium graminearum, and Rhizoctonia solani with EC50 values of 0.780, 3.62, 1.59, and 2.85 μg/mL, respectively. Compound A7 showed apparent antibacterial activities toward Xanthomonas oryzae pv. oryzae with a minimum inhibitory concentration (MIC) value of 3.12 μg/mL. Significantly, in vivo antifungal activity suggested that the curative effect (98.3%) of compound D7 was comparable to that of the positive control azoxystrobin (96.7%) at 100 μg/mL. Preliminary mechanistic studies showed that compound D7 might cause mycelial abnormality of S. sclerotiorum, cell membrane breakage, accumulation of reactive oxygen species (ROS), and inhibition of sclerotia formation. Therefore, compound D7 could be a novel broad-spectrum fungicidal candidate against plant fungal diseases. © 2022 American Chemical Society
KeywordAlkaloids Cytology Metabolites Microorganisms Plants (botany) Anti-bacterial activity Anti-microbial activity Cryptolepine Design activity Design synthesis Fungicidal activity Quindoline Sclerotinia Sclerotiorum Structure-activity relationship. Structure-activity relationships quindoline cryptolepine alkaloid antimicrobial activity Sclerotinia sclerotiorum structure-activity relationship
PublisherAmerican Chemical Society
DOI10.1021/acs.jafc.1c07536
Indexed ByEI ; SCIE
Language英语
WOS Research AreaAgriculture ; Chemistry ; Food Science & Technology
WOS SubjectAgriculture, Multidisciplinary ; Chemistry, Applied ; Food Science & Technology
WOS IDWOS:000767891600007
EI Accession Number20221111784484
EI KeywordsFungicides
EI Classification Number461.2 Biological Materials and Tissue Engineering ; 461.9 Biology ; 804 Chemical Products Generally ; 804.1 Organic Compounds
Original Document TypeJournal article (JA) ; Article
Citation statistics
Cited Times:9[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttps://ir.lzu.edu.cn/handle/262010/477926
Collection药学院
Corresponding AuthorLiu, Ying-Qian
Affiliation
1.School of Pharmacy, Lanzhou University, Lanzhou; 730000, China;
2.State Key Laboratory of Grassland Agro-ecosystems, Lanzhou University, Lanzhou; 730000, China
First Author AffilicationSchool of Pharmacy
Corresponding Author AffilicationSchool of Pharmacy;  Lanzhou University
Recommended Citation
GB/T 7714
Chu, Qing-Ru,He, Ying-Hui,Tang, Chen,et al. Design, Synthesis, and Antimicrobial Activity of Quindoline Derivatives Inspired by the Cryptolepine Alkaloid[J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,2022,70(9):2851-2863.
APA Chu, Qing-Ru.,He, Ying-Hui.,Tang, Chen.,Zhang, Zhi-Jun.,Luo, Xiong-Fei.,...&Liu, Ying-Qian.(2022).Design, Synthesis, and Antimicrobial Activity of Quindoline Derivatives Inspired by the Cryptolepine Alkaloid.JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,70(9),2851-2863.
MLA Chu, Qing-Ru,et al."Design, Synthesis, and Antimicrobial Activity of Quindoline Derivatives Inspired by the Cryptolepine Alkaloid".JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY 70.9(2022):2851-2863.
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