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  • 降毛荚醛

    Norviburtinal

    降毛荚醛
    产品编号 CFN97411
    CAS编号 85051-41-8
    分子式 = 分子量 C9H6O2 = 146.1
    产品纯度 >=98%
    物理属性 Yellow powder
    化合物类型 Iridoids
    植物来源 The herbs of Cerbera manghas L.
    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
    降毛荚醛 CFN97411 85051-41-8 1mg QQ客服:2056216494
    降毛荚醛 CFN97411 85051-41-8 5mg QQ客服:2056216494
    降毛荚醛 CFN97411 85051-41-8 10mg QQ客服:2056216494
    降毛荚醛 CFN97411 85051-41-8 20mg QQ客服:2056216494
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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
    我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
  • Shanghai Institute of Biochemistry and Cell Biology (China)
  • University of Sao Paulo (Brazil)
  • Yale University (USA)
  • Chinese University of Hong Kong (China)
  • University of Maryland School of Medicine (USA)
  • University of Wuerzburg (Germany)
  • Max Rubner-Institut (MRI) (Germany)
  • Fraunhofer-Institut für Molekularbiologie und Angewandte ?kologie IME (Germany)
  • Weizmann Institute of Science (Israel)
  • Monash University (Australia)
  • Kyoto University (Japan)
  • University of Oslo (Norway)
  • University of Medicine and Pharmacy (Romania)
  • Instituto Politécnico de Bragan?a (Portugal)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Neuropharmacology.2018, 131:68-82
  • Spectrochim Acta A2019, 210:372-380
  • Chem Biol Interact.2022, 368:110248.
  • J Biotechnol.2020, 318:10-19.
  • Vietnam J. Chemistry2022, 60(2):211-222
  • Research Square2021, 10.21203.
  • RSC Adv.2023, 13(9):6317-6326.
  • Plants (Basel).2020, 9(11):1535.
  • Food Chem.2023, 404(Pt A):134517.
  • J Appl Microbiol.2022, 132(2):949-963.
  • Oxid Med Cell Longev.2020, 2020:8887251.
  • Clin Transl Med.2021, 11(5):e392.
  • Turkish Journal of Pharmaceutical Sciences2022, DOI: 10.4274
  • Neurotoxicology.2022, 91:218-227.
  • Food Res Int.2022, 157:111207.
  • Korean J. Food Preserv. 2021, 28(6):846-856.
  • Polytechnic University of Catalonia2017, 105826
  • Molecules.2022, 27(2):451.
  • J Appl Biol Chem.2022, 65(4):pp.463-469.
  • Cancers (Basel).2021, 13(17):4327.
  • J of Applied Biological Chem.2020, 63(2):147-152
  • Heliyon.2023, e12684.
  • J Nat Prod.2019, 82(4):1002-1008
  • ...
  • 生物活性
    Description: Norviburtinal possesses novel angiogenesis effect. Norviburtinal and isopinnatal show in vitro cytotoxicity against cancer cell lines, norviburtinal has little selectivity for melanoma cell lines whilst isopinnatal also shows some cytotoxic activity.
    In vitro:
    Planta Med. 2000 Dec;66(8):758-61.
    In vitro cytotoxicity of norviburtinal and isopinnatal from Kigelia pinnata against cancer cell lines.[Pubmed: 11199138]

    METHODS AND RESULTS:
    Crude dichloromethane extracts of Kigelia pinnata stem bark and fruit showed cytotoxic activity in vitro against cultured melanoma and other cancer cell lines using the Sulphorhodamine B assay, which was used for bioassay-guided fractionation. Thin layer chromatography (TLC) examination of the most active fractions of both stem bark and fruits showed the presence of the same major components which were found to be Norviburtinal and beta-sitosterol. Norviburtinal was found to be the most active compound but had little selectivity for melanoma cell lines whilst isopinnatal also showed some cytotoxic activity. beta-Sitosterol was found to be comparatively inactive.
    CONCLUSIONS:
    HPLC analysis of the crude extract showed that the amount of Norviburtinal present in the plant material did not account for all of the activity of the total extracts.
    In vivo:
    J Ethnopharmacol. 2011 Oct 11;137(3):1323-7.
    Bioassay-guided isolation of norviburtinal from the root of Rehmannia glutinosa, exhibited angiogenesis effect in zebrafish embryo model.[Pubmed: 21843616 ]
    The root of Rehmannia glutinosa (RR) is commonly used as a wound-healing agent in various traditional Chinese herbal formulae; while angiogenesis is one of the crucial aspects in wound-healing. The objective of the present study was to investigate the angiogenesis effects of RR aqueous crude extract and its active component(s) using zebrafish model.
    METHODS AND RESULTS:
    The in vivo angiogenesis effect was studied using transgenic TG(fli1:EGFP)(y1)/+(AB) zebrafish embryos by observing the capillary sprouts formation in sub-intestinal vessel (SIV) of zebrafish embryos after 72 h post-fertilization under fluorescence microscopy. Our results indicated that RR aqueous crude extract (250 μg/ml) exhibited significant angiogenesis effect, with an increase in capillary sprouts formation in SIV. Following sequential solvent partition of the RR aqueous crude extract with dichloromethane, ethyl acetate and n-butanol successively, the dichloromethane fraction (DCM) was found to have the most sprouts formation in the SIV region. Subjected to column chromatography, DCM fraction was further fractionated into six sub-fractions and among these tested, the sub-fraction C2 exhibited the most potent angiogenesis effect. The major component, C2A, was isolated and identified as norviburtinal using nuclear magnetic resonance (NMR) and mass spectrometry (MS). The compound norviburtinal (at 50 μg/ml) was shown to possess significant angiogenesis effect in zebrafish model (p < 0.001).
    CONCLUSIONS:
    Norviburtinal was, for the first time, found in the extract of RR and possessed novel angiogenesis effect. Bioassay-guided fractionation suggested that norviburtinal was not the only active component responsible for the angiogenesis effect of RR.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 6.8446 mL 34.2231 mL 68.4463 mL 136.8925 mL 171.1157 mL
    5 mM 1.3689 mL 6.8446 mL 13.6893 mL 27.3785 mL 34.2231 mL
    10 mM 0.6845 mL 3.4223 mL 6.8446 mL 13.6893 mL 17.1116 mL
    50 mM 0.1369 mL 0.6845 mL 1.3689 mL 2.7379 mL 3.4223 mL
    100 mM 0.0684 mL 0.3422 mL 0.6845 mL 1.3689 mL 1.7112 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
    戊曲酯,缬草三酯; Valepotriate CFN90205 18296-44-1 C22H30O8 = 422.47 20mg QQ客服:2159513211
    地戊曲酯; Didrovaltrate CFN96822 18296-45-2 C22H32O8 = 424.49 5mg QQ客服:215959384
    IVHD-valtrate; IVHD-valtrate CFN96823 28325-56-6 C27H40O11 = 540.60 5mg QQ客服:2056216494
    醋戊曲酯; Acevaltrate CFN96825 25161-41-5 C24H32O10 = 480.51 10mg QQ客服:2056216494
    缬草苦苷; Valerosidate CFN96457 29505-31-5 C21H34O11 = 462.49 5mg QQ客服:1457312923
    Valeriotriate B; Valeriotriate B CFN96458 862255-64-9 C27H42O12 = 558.62 5mg QQ客服:1457312923
    Valeriotetrate C; Valeriotetrate C CFN96459 904891-20-9 C37H58O15 = 742.85 5mg QQ客服:2056216494
    Jatamanvaltrate B ; Jatamanvaltrate B CFN96826 1134138-66-1 C32H50O13 = 642.73 5mg QQ客服:3257982914
    氯化缬草素; Valechlorine CFN90622 51771-49-4 C22H31ClO8 = 458.93 5mg QQ客服:2056216494
    Valeriandoid B; Valeriandoid B CFN96460 1380399-57-4 C24H33ClO10 = 516.97 5mg QQ客服:1457312923

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