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  • (+)-花旗松素

    (+)-Taxifolin

    (+)-花旗松素
    产品编号 CFN99183
    CAS编号 17654-26-1
    分子式 = 分子量 C15H12O7 = 304.25
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Flavonoids
    植物来源 The herbs of Silybum marianum (L.) Gaertn.
    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
    (+)-花旗松素 CFN99183 17654-26-1 10mg QQ客服:2056216494
    (+)-花旗松素 CFN99183 17654-26-1 20mg QQ客服:2056216494
    (+)-花旗松素 CFN99183 17654-26-1 50mg QQ客服:2056216494
    (+)-花旗松素 CFN99183 17654-26-1 100mg 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
  • Sanford Burnham Prebys Medical Discovery Institute (USA)
  • University of Auckland (New Zealand)
  • Tohoku University (Japan)
  • University of Wollongong (Australia)
  • Auburn University (USA)
  • Monash University Malaysia (Malaysia)
  • Universidade Católica Portuguesa (Portugal)
  • Universidade Federal de Goias (UFG) (Brazil)
  • University of Leipzig (Germany)
  • Technical University of Denmark (Denmark)
  • University of Wisconsin-Madison (USA)
  • Max-Planck-Insitut (Germany)
  • Amity University (India)
  • Seoul National University of Science and Technology (Korea)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Front Pharmacol.2022, 13:883475.
  • Sci Rep. 2017, 17332(7)
  • Exp Neurobiol.2018, 27(3):200-209
  • Pharmacological Reports2020, 1-9
  • Microorganisms.2021, 9(12):2514.
  • Regul Toxicol Pharmacol.2023, 142:105433.
  • J Nat Med.2017, 71(2):457-462
  • Nat Prod Sci.2019, 25(3):238
  • J of Dentistry & Oral Health2019, 2641-1962
  • J Agric Food Chem.2019, 67(27):7748-7754
  • Planta Med.2016, 82(13):1208-16
  • J Food Biochem.2020, 44(6):e13198.
  • ACS Omega.2021, 6(36):23460-23474.
  • Korean J. Food Preserv. 2021, 28(6):846-856.
  • Plant Physiol Biochem.2023, 201:107795.
  • Chem. of Vegetable Raw Materials2020, 97-105
  • Nutrients.2022, 14(23):4997.
  • Biomedicines.2022, 10(2):463.
  • J.Food Processing & Preservation2022, jfpp.16666
  • Int J Mol Sci.2021, 22(14):7324.
  • Chem Pharm Bull (Tokyo).2017, 65(9):826-832
  • Journal of Third Military Medical University2018, 40(12):1073-1078
  • Pharmacogn Mag.2015, 11(43):562-6
  • ...
  • 生物活性
    Description: (+)-Taxifolin is an inhibitor of aggregation of the 42-residue amyloid β-protein, it has preventive effects against Alzheimer's disease-like pathogenesis in vivo. It is also a weak inhibitor of cytochrome b5 reduction (IC50=9.8μM).
    Targets: Beta Amyloid
    In vitro:
    Toxicology. 2013 Jun 7;308:34-40.
    In vitro effects of myricetin, morin, apigenin, (+)-taxifolin, (+)-catechin, (-)-epicatechin, naringenin and naringin on cytochrome b5 reduction by purified NADH-cytochrome b5 reductase.[Pubmed: 23567315 ]
    The microsomal NADH-dependent electron transport system consisting of cytochrome b5 reductase and cytochrome b5 participates in a number of physiologically important processes including lipid metabolism as well as is involved in the metabolism of various drug and xenobiotics.
    METHODS AND RESULTS:
    In the present study, we assessed the inhibitory effects of eight dietary flavonoids representing five distinct chemical classes on cytochrome b5 reduction by purified cytochrome b5 reductase. From the flavonoids tested, myricetin was the most potent in inhibiting cytochrome b5 reduction with an IC50 value of 0.35μM. Myricetin inhibited b5 reductase noncompetitively with a Ki of 0.21μM with respect to cofactor NADH, and exhibited a non-linear relationship indicating non-Michaelis-Menten kinetic binding with respect to cytochrome b5. In contrast to the potent inhibitory activity of myricetin, (+)-Taxifolin was found to be a weak inhibitor (IC50=9.8μM). The remaining flavonoids were inactive within the concentration range tested (1-50μM). Analysis of structure-activity data suggested that simultaneous presence of three OH groups in ring B is a primary structural determinant for a potent enzyme inhibition.
    CONCLUSIONS:
    Our results suggest that inhibition of the activity of this system by myricetin or myricetin containing diets may influence the metabolism of therapeutic drugs as well as detoxification of xenobiotics.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.2868 mL 16.4339 mL 32.8677 mL 65.7354 mL 82.1693 mL
    5 mM 0.6574 mL 3.2868 mL 6.5735 mL 13.1471 mL 16.4339 mL
    10 mM 0.3287 mL 1.6434 mL 3.2868 mL 6.5735 mL 8.2169 mL
    50 mM 0.0657 mL 0.3287 mL 0.6574 mL 1.3147 mL 1.6434 mL
    100 mM 0.0329 mL 0.1643 mL 0.3287 mL 0.6574 mL 0.8217 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
    茯苓酸AM; Poricoic acid AM CFN91538 151200-92-9 C32H48O5 = 512.7 5mg QQ客服:3257982914
    氯化飞燕草素-3,5-O-二葡萄糖苷; Delphinidin-3,5-O-diglucoside chloride CFN92137 17670-06-3 C27H31O17Cl = 663.0 5mg QQ客服:2159513211
    大豆皂苷Ac; Soyasaponin Ac CFN90774 133882-74-3 C67H104O32 = 1421.6 5mg QQ客服:215959384
    柯里拉京; Corilagin CFN90176 23094-69-1 C27H22O18 = 634.45 20mg QQ客服:1413575084

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