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  • 闹羊花毒素III

    Rhodojaponin III

    闹羊花毒素III
    产品编号 CFN90673
    CAS编号 26342-66-5
    分子式 = 分子量 C20H32O6 = 368.47
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Diterpenoids
    植物来源 The herbs of Rhododendron molle G. Don
    ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用
    提供自定义包装
    产品名称 产品编号 CAS编号 包装 QQ客服
    闹羊花毒素III CFN90673 26342-66-5 1mg QQ客服:1457312923
    闹羊花毒素III CFN90673 26342-66-5 5mg QQ客服:1457312923
    闹羊花毒素III CFN90673 26342-66-5 10mg QQ客服:1457312923
    闹羊花毒素III CFN90673 26342-66-5 20mg QQ客服:1457312923
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    ChemFaces的产品在许多优秀和顶级科学期刊中被引用

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.
    IF=36.216(2019)

    PMID: 29328914

    Cell Metab. 2020 Mar 3;31(3):534-548.e5.
    doi: 10.1016/j.cmet.2020.01.002.
    IF=22.415(2019)

    PMID: 32004475

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.
    IF=14.548(2019)

    PMID: 29149595

    ACS Nano. 2018 Apr 24;12(4): 3385-3396.
    doi: 10.1021/acsnano.7b08969.
    IF=13.903(2019)

    PMID: 29553709

    Nature Plants. 2016 Dec 22;3: 16206.
    doi: 10.1038/nplants.2016.205.
    IF=13.297(2019)

    PMID: 28005066

    Sci Adv. 2018 Oct 24;4(10): eaat6994.
    doi: 10.1126/sciadv.aat6994.
    IF=12.804(2019)

    PMID: 30417089
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  • University of Perugia (Italy)
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  • University of Lodz (Poland)
  • Agricultural Research Organization (ARO) (Israel)
  • Helmholtz Zentrum München (Germany)
  • Center for protein Engineering (CIP) (Belgium)
  • VIB Department of Plant Systems Biology, UGent (PSB) (Belgium)
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  • Universidad de Antioquia (Colombia)
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  • Universidad Miguel Hernández (Spain)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Pharmaceuticals.2022, 15(4), 402.
  • Journal of Food Quality2022, P:13, 6256310.
  • SCOPUS.2020, 836-847.
  • Int J Oncol.2016, 49(4):1497-504
  • Hum Exp Toxicol.2023, 42:9603271221145386.
  • Clin Exp Pharmacol Physiol.2015, 42(11):1189-97
  • Plant Cell,Tissue & Organ Culture2016, 127(1):115-121
  • Nat Commun.2021, 12(1):681.
  • Molecules.2019, 24(2):E343
  • Food and Fermentation Industries2019, 45(7):45-51
  • Pharmaceuticals (Basel).2021, 14(7):633.
  • Environ Toxicol.2020, doi: 10.1002
  • Molecules.2017, 22(3)
  • Food Chem.2018, 252:207-214
  • Russian J Bioorganic Chemistry 2021, 47:1411-1417.
  • Pest Manag Sci.2023, 79(8):2675-2685.
  • Journal of Functional Foods2022, 99: 105331.
  • Phytomedicine.2018, 38:12-23
  • Food Research International2020, 108987
  • Evid Based Complement Alternat Med.2021, 2021:8850744.
  • Biochem Biophys Res Commun.2018, 505(1):194-200
  • Front Pharmacol.2021, 12:615157.
  • University of Central Lancashire2017, 20472
  • ...
  • 生物活性
    Description: Rhodojaponin III has antifeedant and oviposition deterrence effects against many kinds of insects, BdorCSP2 of B. dorsalis could be involved in chemoreception of Rhodojaponin III and played a critical role. Rhodojaponin III induces a certain linkage for change of [Ca2+](i), cell cycle arrest, proliferation inhibition in Sf9 cells.
    Targets: Calcium Channel
    In vitro:
    Arch Insect Biochem Physiol. 2014 Jun;86(2):122-36.
    Contacting is essential for oviposition deterrence of Rhodojaponin-III in Spodoptera litura.[Pubmed: 24782249]
    In Lepidoptera, choosing the right site for egg laying is particularly important, because the small larvae cannot forage for alternate host plants easily. Some secondary compounds of plants have the ability to deter oviposition behaviors of insects.
    METHODS AND RESULTS:
    Rhodojaponin III, a botanical compound, has been reported to have intense deterring-oviposition activity against many insects, which have important implications for agricultural pest management. This study provided evidence for elucidating the perception mechanism underlying Rhodojaponin III as oviposition deterrent. In this study, the antennas of moths could not elicit notable electroantennogram responses to Rhodojaponin III, which suggested the Rhodojaponin III could not exert effects like those volatile compounds. The results of physiological experiments confirmed the Rhodojaponin III could produce the oviposition deterrence effect against moths without depending on antennas, while the physical contact was essential for perceiving the compound, which suggested that the sensilla on tarsus and ovipositor could be chemoreceptor for Rhodojaponin III. Therefore, these sensilla were investigated by scanning electron microscopy to explore their potential functions in detecting Rhodojaponin III.
    CONCLUSIONS:
    This study highlighted the contacting mechanism in deterring oviposition behaviors of moths by Rhodojaponin III and provided new insight for development of contact-based pest management.
    PLoS One. 2013 Jul 5;8(7):e67723.
    Proteomic and properties analysis of botanical insecticide rhodojaponin III-induced response of the diamondback moth, Plutella xyllostella (L.).[Pubmed: 23861792]
    Rhodojaponin III, as a botanical insecticide, affects a wide variety of biological processes in insects, including reduction of feeding, suspension of development, and oviposition deterring of adults in a dose-dependent manner. However, the mode of these actions remains obscure.
    METHODS AND RESULTS:
    In this study, a comparative proteomic approach was adopted to examine the effect of Rhodojaponin III on the Plutella xyllostella (L.). Following treating 48 hours, newly emergence moths were collected and protein samples were prepared. The proteins were separated by 2-DE, and total 31 proteins were significantly affected by Rhodojaponin III compared to the control identified by MALDI-TOF/TOF-MS/MS. These differentially expressed proteins act in the nervous transduction, odorant degradation and metabolic change pathways. Further, gene expression patterns in treated and untreated moths were confirmed by qRT-PCR and western blot analysis. RNAi of the chemosensory protein (PxCSP) gene resulted in oviposition significantly increased on cabbage plants treated with Rhodojaponin III.
    CONCLUSIONS:
    These Rhodojaponin III-induced proteins and gene properties analysis would be essential for a better understanding of the potential molecular mechanism of the response to Rhodojaponin III from moths of P. xylostella.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.7139 mL 13.5696 mL 27.1393 mL 54.2785 mL 67.8481 mL
    5 mM 0.5428 mL 2.7139 mL 5.4279 mL 10.8557 mL 13.5696 mL
    10 mM 0.2714 mL 1.357 mL 2.7139 mL 5.4279 mL 6.7848 mL
    50 mM 0.0543 mL 0.2714 mL 0.5428 mL 1.0856 mL 1.357 mL
    100 mM 0.0271 mL 0.1357 mL 0.2714 mL 0.5428 mL 0.6785 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    部分图片展示
    产品名称 产品编号 CAS编号 分子式 = 分子量 位单 联系QQ
    银杏内酯A; Ginkgolide A CFN99638 15291-75-5 C20H24O9 = 408.4 20mg QQ客服:1413575084
    银杏内酯J; Ginkgolide J CFN99149 107438-79-9 C20H24O10 = 424.40 20mg QQ客服:1413575084
    银杏内酯B; Ginkgolide B CFN99640 15291-77-7 C20H24O10 = 424.4 20mg QQ客服:3257982914
    银杏内酯C; Ginkgolide C CFN99639 15291-76-6 C20H24O11 = 440.4 20mg QQ客服:1457312923
    银杏内酯K; Ginkgolide K CFN91009 153355-70-5 C20H22O9 = 406.4 20mg QQ客服:3257982914
    Gopherenediol; Gopherenediol CFN96287 916236-79-8 C20H34O2 = 306.5 5mg QQ客服:2056216494
    闹羊花毒素II; Rhodojaponin II CFN90674 26116-89-2 C22H34O7 = 410.51 10mg QQ客服:2056216494
    闹羊花毒素III; Rhodojaponin III CFN90673 26342-66-5 C20H32O6 = 368.47 10mg QQ客服:2159513211
    闹羊花毒素V; Rhodojaponin V CFN90670 37720-86-8 C22H34O7 = 410.5 10mg QQ客服:1413575084
    20-脱羟基伊桐素B; Itol A CFN99049 1033747-78-2 C20H32O6 = 368.5 5mg QQ客服:1413575084

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