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  • 羊蹄素

    Nepodin

    羊蹄素
    产品编号 CFN96584
    CAS编号 3785-24-8
    分子式 = 分子量 C13H12O3 = 216.24
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Phenols
    植物来源 The roots of Rumex nepalensis.
    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
    羊蹄素 CFN96584 3785-24-8 1mg QQ客服:1413575084
    羊蹄素 CFN96584 3785-24-8 5mg QQ客服:1413575084
    羊蹄素 CFN96584 3785-24-8 10mg QQ客服:1413575084
    羊蹄素 CFN96584 3785-24-8 20mg QQ客服:1413575084
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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
  • University of Lodz (Poland)
  • Max Rubner-Institut (MRI) (Germany)
  • University of Padjajaran (Indonesia)
  • The University of Newcastle (Australia)
  • University of Amsterdam (Netherlands)
  • Yale University (USA)
  • Aarhus University (Denmark)
  • Kyung Hee University (Korea)
  • Universiti Sains Malaysia (Malaysia)
  • Center for protein Engineering (CIP) (Belgium)
  • Chiang Mai University (Thailand)
  • Uniwersytet Medyczny w ?odzi (Poland)
  • University of Melbourne (Australia)
  • University of Wuerzburg (Germany)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Anal Bioanal Chem.2020, 412(12):3005-3015.
  • Journal of Functional Foods2022, 99: 105331.
  • ACS Nano.2018, 12(4):3385-3396
  • J of the Korean Society of Food Science and Nutrition2019, 32(2):148-154
  • Phytomedicine2022, 104:154318
  • Molecules.2021, 26(6):1738.
  • Molecules.2021, 26(4):817.
  • Int Immunopharmacol.2023, 7:127:111322.
  • Int Immunopharmacol.2022, 106:108603.
  • Biomed Pharmacother.2019, 116:108987
  • Phytomedicine.2020, 79, 153351
  • J Ethnopharmacol.2023, 321:117501.
  • Sci Rep.2019, 9(1):4646
  • Vietnam Journal of Science2022, 64(2), 69-75.
  • Phytomedicine.2022, 100:154036.
  • J Chromatogr B Analyt Technol Biomed Life Sci.2021, 1187:123012.
  • Evid Based Complement Alternat Med.2020, 2020:1970349.
  • Green Chemistry2021, ISSUE 2.
  • J Sep Sci.2018, 41(9):1938-1946
  • Auburn University2015, 1-58
  • Pak J Pharm Sci.2018, 31:311-315
  • Evid Based Complement Alternat Med.2017, 2017:1583185
  • The Japan Society for Analy. Chem.2017, 66(8):613-617
  • ...
  • 生物活性
    Description: Nepodin has antimalarial, and anti-inflammatory activities, it shows significant cyclooxygenase (COX) inhibitory activity. Nepodin has an antidiabetic effect, which is at least partly mediated by stimulation of GLUT4 translocation via AMPK activation by nepodin.
    Targets: COX | AMPK | GLUT | Antifection
    In vitro:
    Biofactors. 2014 Jul-Aug;40(4):436-47.
    Antidiabetic effect of nepodin, a component of Rumex roots, and its modes of action in vitro and in vivo.[Pubmed: 24756979 ]
    Many active components derived from edible natural resources such as plant extracts have recently attracted attention for their potential use as functional foods or drugs for preventing and treating metabolic diseases such as diabetes.
    METHODS AND RESULTS:
    To obtain a novel modulator of glucose metabolism, we conducted screening of a small compound library in cultured L6 myotubes. We identified nepodin that stimulated glucose uptake dose-dependently in differentiated L6 myotubes. The stimulatory effect of nepodin on glucose uptake was abrogated by a 5'-adenosine monophosphate-activated protein kinase (AMPK) inhibitor. In addition, nepodin stimulated the phosphorylation of AMPK. Nepodin also stimulated the translocation of GLUT4 to the plasma membrane in L6 myoblasts transfected with a Glut4 cDNA-coding vector and in differentiated L6 myotubes. In in vivo study, nepodin suppressed the increases in fasting blood glucose levels and improved the glucose intolerance of C57BL/KsJ-db/db mice, a type 2 diabetic animal model. Nepodin rescued the impaired phosphorylation of AMPK in the skeletal muscle of db/db mice.
    CONCLUSIONS:
    These results suggest that nepodin has an antidiabetic effect, which is at least partly mediated by stimulation of GLUT4 translocation via AMPK activation by nepodin.
    Arch Pharm Res. 2013 Apr;36(4):430-5.
    Antimalarial activity of nepodin isolated from Rumex crispus.[Pubmed: 23440579 ]
    The purpose of this study is to define the antimalarial activity of Rumex crispus.
    METHODS AND RESULTS:
    To identify an active compound that is isolated from R. crispus, bioassay-based chromatographic fractionation and purification is carried out from 70 % ethanol extract of R. crispus; then, an active compound, nepodin, is identified by spectroscopic analysis. Anitmalarial activity is measured by PfNDH2 assay, cytotoxicity, and animal test. From NADH:quinone oxidoreductase enzyme (PfNDAH2) assay, nepodin exhibited significant IC50 values that were 0.74 ± 0.07 and 0.79 ± 0.06 μg/ml against P. falciparum chloroquine-sensitive (3D7) and P. falciparum chloroquine-resistant (S20), respectively. Nepodin showed a potential selective inhibition (SI index: ratio of 50 % cytotoxic concentration to 50 % effective anti-plasmodial concentration) of 161.6 and 151.4 against P. falciparum 3D7 and P. falciparum S20. In the animal test, all groups of nepodin treatment of 10, 50, and 250 mg/kg were active with a parasitemia suppression of 97.1 ± 3.3, 99.1 ± 3.7, and 99.1 ± 2.6 %, respectively. The survival time with nepodin treatment was increased by 14.6 ± 2.5, 16.2 ± 1.5, and 19.8 ± 1.7 days at each dose, respectively.
    CONCLUSIONS:
    This study newly identified the plant R. crispus containing nepodin, which is a potential antimalarial compound. It exhibited the inhibitory activity of PfNDH2 and prolonged the survival time on the group of nepodin treatment; moreover, it inhibited the parasitemia in the animal test.
    J Agric Food Chem. 2012 Oct 24;60(42):10415-9.
    Isolation and identification of Flavobacterium columnare and Streptococcus iniae antibacterial compounds from the terrestrial plant Atraphaxis laetevirens.[Pubmed: 23030835 ]
    Columnaris disease, enteric septicemia of catfish, and streptococcosis are common bacterial diseases of certain freshwater fish and are caused by Flavobacterium columnare , Edwardsiella ictaluri , and Streptococcus iniae , respectively.
    METHODS AND RESULTS:
    During the process of evaluating several species of plants to isolate and identify compounds with toxicity against these bacteria, a promising extract from the aerial parts of the terrestrial plant Atraphaxis laetevirens (Ledeb.) Jaub. et Spach (Polygonaceae Juss.) was selected for bioassay-guided fractionation using a rapid microplate bioassay. The active dichloromethane extract was subjected to liquid-liquid partitioning, and active fractions were further separated by normal-phase column chromatography and normal-phase high-performance liquid chromatography (HPLC). Nepodin (3) and emodin (4) were isolated from two fractions with strong toxicities against S. iniae .
    CONCLUSIONS:
    A chloroform fraction was further separated by normal-phase column chromatography to yield two active fractions against F. columnare , and these fractions contained chrysophanol (1), physcion (2), and Nepodin (3). Compound 1 had strong activity, and compound 3 had moderate activity against F. columnare , while compounds 2 and 4 were not toxic at the concentrations tested.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 4.6245 mL 23.1225 mL 46.2449 mL 92.4898 mL 115.6123 mL
    5 mM 0.9249 mL 4.6245 mL 9.249 mL 18.498 mL 23.1225 mL
    10 mM 0.4624 mL 2.3122 mL 4.6245 mL 9.249 mL 11.5612 mL
    50 mM 0.0925 mL 0.4624 mL 0.9249 mL 1.8498 mL 2.3122 mL
    100 mM 0.0462 mL 0.2312 mL 0.4624 mL 0.9249 mL 1.1561 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
    羊蹄素; Nepodin CFN96584 3785-24-8 C13H12O3 = 216.24 5mg QQ客服:1457312923
    芦荟大黄素 8-葡萄糖甙; Torachrysone 8-O-glucoside CFN97101 64032-49-1 C20H24O9 = 408.4 20mg QQ客服:1457312923
    Cassiaglycoside II; Cassiaglycoside II CFN95130 2241081-56-9 C25H32O14 = 556.5 5mg QQ客服:3257982914
    Torosachrysone 8-O-beta-gentiobioside; Torosachrysone 8-O-beta-gentiobioside CFN95131 94356-13-5 C28H36O15 = 612.6 5mg QQ客服:215959384
    马兜铃酸C; Aristolochic acid C CFN90516 4849-90-5 C16H9NO7 = 327.25 20mg QQ客服:2056216494
    马兜铃酸A; Aristolochic acid A CFN99505 313-67-7 C17H11O7N = 341.27 20mg QQ客服:215959384
    7-羟基马兜铃酸 A; 7-Hydroxyaristolochic acid A CFN90517 79185-75-4 C17H11NO8 = 357.3 20mg QQ客服:2159513211
    马兜铃酸D; Aristolochic acid D CFN90783 17413-38-6 C17H11NO8 = 357.3 10mg QQ客服:3257982914
    2-(7-甲氧基萘-1-基)乙腈; 7-Methoxy-1-naphthylacetonitrile CFN90086 138113-08-3 C13H11NO = 197.23 5mg QQ客服:2159513211
    2-(7-甲氧基萘-1-基)乙胺盐酸盐; 2-(7-Methoxy-1-naphthyl)ethylamine hydrochloride CFN90089 139525-77-2 C13H15NO.HCl = 237.73 5mg QQ客服:3257982914

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