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  • 异土大黄苷

    Isorhapontin

    异土大黄苷
    产品编号 CFN91655
    CAS编号 32727-29-0
    分子式 = 分子量 C21H24O9 = 420.4
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Phenols
    植物来源 The roots of Rumex obtusifolius 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
    异土大黄苷 CFN91655 32727-29-0 1mg QQ客服:2056216494
    异土大黄苷 CFN91655 32727-29-0 5mg QQ客服:2056216494
    异土大黄苷 CFN91655 32727-29-0 10mg QQ客服:2056216494
    异土大黄苷 CFN91655 32727-29-0 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
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  • Instytut Nawozów Sztucznych w Pu?awach (Poland)
  • Universidade do Porto (Portugal)
  • Melbourne University (Australia)
  • Calcutta University (India)
  • Nicolaus Copernicus Uniwersity (Poland)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Nutrients.2023, 15(6):1335.
  • J Clin Med.2022, 11(13):3662.
  • Sci Rep.2017, 7:46299
  • Molecules.2016, 21(6)
  • J Asian Nat Prod Res.2019, 5:1-17
  • Metabolites.2020, 11(1):E11.
  • Asian Pac J Cancer Prev. 2020, 21(4):935-941.
  • Food Chem. 2020, 320:126530
  • Pharmaceuticals (Basel).2022, 15(8):982.
  • Plants (Basel).2024, 13(6):868.
  • Front Immunol.2018, 9:2655
  • Phytomedicine.2024, 125:155350.
  • Pharmaceuticals (Basel).2022, 15(5):591.
  • Phytochem Anal.2024, pca.3319.
  • Anal Chim Acta.2021, 1180:338874.
  • Int J Mol Sci.2020, 21(9):3144.
  • Anal Bioanal Chem.2018, 410(5):1561-1569
  • Sci Rep.2023, 13(1):13072.
  • Mol Neurobiol.2022, 02873-9.
  • Plant Cell Tiss Org2020, 1-16
  • Inflammation.2020, 43(5):1716-1728.
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  • Nanotechnology.2024, ad470d.
  • ...
  • 生物活性
    Description: Isorhapontin is a stilbenoids compound with antioxidant, antibacterial and antifungal properties.
    In vitro:
    Int J Food Microbiol . 2013 Jun 3;164(1):99-107.
    The antimicrobial effects of wood-associated polyphenols on food pathogens and spoilage organisms[Pubmed: 23624538]
    The antimicrobial effects of the wood-associated polyphenolic compounds pinosylvin, pinosylvin monomethyl ether, astringin, piceatannol, isorhapontin, isorhapontigenin, cycloXMe, dHIMP, ArX, and ArXOH were assessed against both Gram-negative (Salmonella) and Gram-positive bacteria (Listeria monocytogenes, Staphylococcus epidermidis, Staphylococcus aureus) and yeasts (Candida tropicalis, Saccharomyces cerevisiae). Particularly the stilbenes pinosylvin, its monomethyl ether and piceatannol demonstrated a clear antimicrobial activity, which in the case of pinosylvin was present also in food matrices like sauerkraut, gravlax and berry jam, but not in milk. The destabilization of the outer membrane of Gram-negative microorganisms, as well as interactions with the cell membrane, as indicated by the NPN uptake and LIVE/DEAD viability staining experiments, can be one of the specific mechanisms behind the antibacterial action. L. monocytogenes was particularly sensitive to pinosylvin, and this effect was also seen in L. monocytogenes internalized in intestinal Caco2 cells at non-cytotoxic pinosylvin concentrations. In general, the antimicrobial effects of pinosylvin were even more prominent than those of a related stilbene, resveratrol, well known for its various bioactivities. According to our results, pinosylvin could have potential as a natural disinfectant or biocide in some targeted applications.
    Plant Mol Biol . 2017 Jun;94(3):229-251.
    Association genetics of phenolic needle compounds in Norway spruce with variable susceptibility to needle bladder rust[Pubmed: 28190131]
    Accumulation of phenolic needle metabolites in Norway spruce is regulated by many genes with small and additive effects and is correlated with the susceptibility against fungal attack. Norway spruce accumulates high foliar concentrations of secondary phenolic metabolites, with important functions for pathogen defence responses. However, the molecular genetic basis underlying the quantitative variation of phenolic compounds and their role in enhanced resistance of spruce to infection by needle bladder rust are unknown. To address these questions, a set of 1035 genome-wide single nucleotide polymorphisms (SNPs) was associated to the quantitative variation of four simple phenylpropanoids, eight stilbenes, nine flavonoids, six related arithmetic parameters and the susceptibility to infection by Chrysomyxa rhododendri in an unstructured natural population of Norway spruce. Thirty-one significant genetic associations for the flavonoids gallocatechin, kaempferol 3-glucoside and quercetin 3-glucoside and the stilbenes resveratrol, piceatannol, astringin and isorhapontin were discovered, explaining 22-59% of phenotypic variation, and indicating a regulation of phenolic accumulation by many genes with small and additive effects. The phenolics profile differed between trees with high and low susceptibility to the fungus, underlining the importance of phenolic compounds in the defence mechanisms of Norway spruce to C. rhododendri. Results highlight the utility of association studies in non-model tree species and may enable marker-assisted selection of Norway spruce adapted to severe pathogen attack.
    Planta Med . 2001 Mar;67(2):158-161.
    Inhibition of xanthine and monoamine oxidases by stilbenoids from Veratrum taliense[Pubmed: 11301865]
    The bioassay guided refractionation of the methanol extract of roots and rhizomes of Veratrum taliense (Liliaceae) yielded five stilbenoids: veraphenol, resveratrol, piceid, isorhapontin, and mulberroside E, all inhibiting xanthine oxidase (XO, EC 1.2.3.2.) in vitro in a dose-dependent manner with IC50 values of 11.0, 96.7, 66.1, 70.0, and 78.4 microM, respectively. Veraphenol and mulberroside E were found to be mixed XO inhibitors with the Ki and Ki data of the former being 32.8 and 239.3 microM, and those of latter 32.5 and 13.8 microM, respectively. However, the inhibition on the enzyme by resveratrol, isorhapontin, and piceid was shown to be competitive with their Ki values of 9.7, 19.1, and 14.3 microM, respectively. Among the five stilbenoids, veraphenol and resveratrol were also revealed to inhibit competitively monoamine oxidase A (MAO, EC 1.4.3.4) with IC50 values at 38.0 and 26.6 microM, and Ki data 36.4 and 47.3 microM, respectively. However, none of the stilbenoids was inhibitory on MAO B in our assay. The structure-activity relationship examination showed that glycosylation of the stilbenoids could reduce the inhibition on XO and diminish the activity against MAO A, indicating that the free phenolic hydroxy group of the compounds was most likely essential for these bioactivities.
    Toxicol Appl Pharmacol . 1996 Feb;136(2):381-388.
    Wood-derived estrogens: studies in vitro with breast cancer cell lines and in vivo in trout[Pubmed: 8619247]
    The wood-derived compound, beta-sitosterol (purity > 90%), was shown to be estrogenic in fish. It induced the expression of the vitellogenin gene in the liver of juvenile and methyltestosterone-treated rainbow trout. Structural similarities to beta-sitosterol notwithstanding, cholesterol, citrostadienol, beta-sitostanol, and 5-androstene-3 beta,17 beta-diol, an estrogenic member of the androstenic steroid group, were inactive. An abietic acid mixture (37% abietic acid, 6% dehydroabietic acid, and a remainder of unknown compounds) showed slight hormonal activity in feed, but it was completely inactive when given intraperitoneally in implants. The estrogenic component of the abietic acid preparation was not identified. In addition, to beta-sitosterol and abietic acid, several other wood-derived compounds including betulin, isorhapontigenin, isorhapontin, and pinosylvin were estrogenic in breast cancer cells (MCF-7 or T-47D). However, betulin and pinosylvin, available in sufficient amounts for in vivo testing, did not induce the expression of the vitellogenin gene. Differences in the primary sequences of human and fish estrogen receptors (hormone as well as DNA-binding regions) or uptake and metabolism of the compounds may explain the discrepancy between the two estrogen bioassays. Wood-derived compounds such as beta-sitosterol, present in pulp and paper mill effluents, may account for the weak estrogenicity of debarking effluent seen at the vitellogenin expression bioassay.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.3787 mL 11.8934 mL 23.7869 mL 47.5737 mL 59.4672 mL
    5 mM 0.4757 mL 2.3787 mL 4.7574 mL 9.5147 mL 11.8934 mL
    10 mM 0.2379 mL 1.1893 mL 2.3787 mL 4.7574 mL 5.9467 mL
    50 mM 0.0476 mL 0.2379 mL 0.4757 mL 0.9515 mL 1.1893 mL
    100 mM 0.0238 mL 0.1189 mL 0.2379 mL 0.4757 mL 0.5947 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
    曲札茋苷、白皮杉醇-3'-O-葡萄糖苷; Piceatannol 3'-O-glucoside CFN90750 94356-26-0 C20H22O9 = 406.4 20mg QQ客服:3257982914
    白皮杉醇葡萄糖苷; Astringin CFN92486 29884-49-9 C20H22O9 = 406.4 5mg QQ客服:3257982914
    毛兰素; Erianin CFN90204 95041-90-0 C18H22O5 = 318.36 20mg QQ客服:215959384
    鼓槌联苄; Chrysotobibenzyl CFN91470 108853-09-4 C19H24O5 = 332.4 5mg QQ客服:3257982914
    氧化白藜芦醇; Oxyresveratrol CFN98368 29700-22-9 C14H12O4 = 244.2 20mg QQ客服:2056216494
    氧化白藜芦醇-2-O-D-吡喃葡萄糖苷; Oxyresveratrol 2-O-beta-D-glucopyranoside CFN90789 392274-22-5 C20H22O9 = 406.4 5mg QQ客服:2159513211
    氧化白藜芦醇-3'-O-β-D-吡喃葡萄糖苷; Oxyresveratrol 3'-O-beta-D-glucopyranoside CFN90793 144525-40-6 C20H22O9 = 406.4 5mg QQ客服:2159513211
    桑皮苷A; Mulberroside A CFN99586 102841-42-9 C26H32O14 = 568.52 20mg QQ客服:1457312923
    cis-桑皮苷A; cis-Mulberroside A CFN95006 166734-06-1 C26H32O14 = 568.52 10mg QQ客服:2159513211
    Gnetucleistol D; Gnetucleistol D CFN92443 629643-26-1 C15H14O4 = 258.3 5mg QQ客服:2056216494

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