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Phytochemistry


Title:Phytotoxic flavonoids from roots of Stellera chamaejasme L. (Thymelaeaceae)
Author(s):Yan Z; Guo H; Yang J; Liu Q; Jin H; Xu R; Cui H; Qin B;
Address:"Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, PR China. Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, PR China; State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, PR China. Electronic address: bqin@licp.cas.cn"
Journal Title:Phytochemistry
Year:2014
Volume:20140802
Issue:
Page Number:61 - 68
DOI: 10.1016/j.phytochem.2014.07.013
ISSN/ISBN:1873-3700 (Electronic) 0031-9422 (Linking)
Abstract:"Allelopathy, the negative effect on plants of chemicals released to the surroundings by a neighboring plant, is an important factor which contributes to the spread of some weeds in plant communities. In this field, Stellera chamaejasme L. (Thymelaeaceae) is one of the most toxic and ecologically-threatening weeds in some of the grasslands of north and west China. Bioassay-guided fractionation of root extracts of this plant led to the isolation of eight flavonoids 1-8, whose structures were elucidated by spectroscopic analysis. All compounds obtained, except 7-methoxylneochaejasmin A (4) and (+)-epiafzelechin (5), showed strong phytotoxic activity against Arabidopsis thaliana seedlings. Seedling growth was reduced by neochamaejasmin B (1), mesoneochamaejasmin A (2), chamaejasmenin C (3), genkwanol A (6), daphnodorin B (7) and dihydrodaphnodorin B (8) with IC50 values of 6.9, 12.1, 43.2, 74.8, 7.1 and 27.3mug/mL, respectively, and all of these compounds disrupted root development. Endogenous auxin levels at the root tips of the A. thaliana DR5::GUS transgenic line were largely reduced by compounds 1, 2 and 6-8, and were increased by compound 4. Moreover, the inhibition rate of A. thaliana auxin transport mutants pin2 and aux1-7 by compounds 1-8 were all lower than the wild type (Col-0). The influence of these compounds on endogenous auxin distribution is thus proposed as a critical factor for the phytotoxic effect. Compounds 1, 2, 4 and 8 were found in soils associated with S. chamaejasme, and these flavonoids also showed phytotoxicity to Clinelymus nutans L., an associated weed of S. chamaejasme. These results indicated that some phytotoxic compounds from roots of S. chamaejasme may be involved in the potential allelopathic behavior of this widespread weed"
Keywords:Allelopathy Arabidopsis/drug effects/metabolism Arabidopsis Proteins/metabolism Flavonoids/*chemistry/isolation & purification Indoleacetic Acids/metabolism Molecular Structure Pheromones/*chemistry Plant Roots/*chemistry Plant Weeds/chemistry Seedlings/d;
Notes:"MedlineYan, Zhiqiang Guo, Hongru Yang, Jiayue Liu, Quan Jin, Hui Xu, Rui Cui, Haiyan Qin, Bo eng Research Support, Non-U.S. Gov't England 2014/08/07 Phytochemistry. 2014 Oct; 106:61-68. doi: 10.1016/j.phytochem.2014.07.013. Epub 2014 Aug 2"

 
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Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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