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  • 鹅掌楸苦素

    Liriodendrin

    鹅掌楸苦素
    产品编号 CFN98964
    CAS编号 573-44-4
    分子式 = 分子量 C34H46O18 = 742.7
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Lignans
    植物来源 The herbs of Linaria vulgaris
    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
    鹅掌楸苦素 CFN98964 573-44-4 1mg QQ客服:2056216494
    鹅掌楸苦素 CFN98964 573-44-4 5mg QQ客服:2056216494
    鹅掌楸苦素 CFN98964 573-44-4 10mg QQ客服:2056216494
    鹅掌楸苦素 CFN98964 573-44-4 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
  • Centrum Menselijke Erfelijkheid (Belgium)
  • University Medical Center Mainz (Germany)
  • Research Unit Molecular Epigenetics (MEG) (Germany)
  • University of Indonesia (Indonesia)
  • Worcester Polytechnic Institute (USA)
  • University of Parma (Italy)
  • Universidad Miguel Hernández (Spain)
  • CSIRO - Agriculture Flagship (Australia)
  • Universidade do Porto (Portugal)
  • University of Beira Interior (Portugal)
  • Aveiro University (Portugal)
  • Chungnam National University (Korea)
  • University of Amsterdam (Netherlands)
  • Shanghai Institute of Biochemistry and Cell Biology (China)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Bioorg Med Chem.2018, 26(14):4201-4208
  • J Agric Food Chem.2020, 68(51):15164-15175
  • The Korea Journal of Herbology2019, 34(2):25-32
  • J Cell Mol Med.2021, 25(5):2645-2654.
  • Anticancer Res.2021, 41(3):1357-1364.
  • J Korean Med Ophthalmol Otolaryngol Dermatol2023, 36(1):21-39.
  • Molecules.2024, 29(6):1240.
  • Planta Med.2022, 88(9-10):794-804.
  • J of App. Res. on Med&Aromatic Plants2020, 100291.
  • Planta Med.2023, 2192-2281
  • Talanta Open2023, 7:100227
  • Biomolecules.2022, 12(12):1754.
  • J Neuroinflammation.2020, 17(1):75.
  • Phytomedicine.2022, 96:153877.
  • Cancers (Basel).2021, 13(9):2223.
  • FASEB J.2019, 33(2):2026-2036
  • Phytomedicine.2019, 58:152893
  • Natural Product Communications2020, doi: 10.1177.
  • Korean J. Food Sci. & Technol.2022, 54(2):241-246
  • FARMACIA2023, Vol.71,3.
  • J Traditional Thai Medical Res.2022, 8(1):pp1-14.
  • Research Square2021, 10.21203.
  • Nutrients2023, 15(18), 4016.
  • ...
  • 生物活性
    Description: Liriodendrin has anti-inflammatory, antinociceptive, hypoglycemic activities, it plays protective role in sepsis-induced acute lung injury, it regulates lung inflammation, the phosphorylation of the NF-kB (p65) and expression of vascular endothelial growth factor (VEGF). Liriodendrin has protective effects on dopamine-induced cytotoxicity via its anti-oxidative properties by reducing ROS level and anti-apoptotic effect via protection of mitochondrion membrane potential (ΔΨm). It may be a potent suppressor of CaCl(2)-induced arrhythmias, the prophylactic administration of liriodendrin is effective in prolonging latency of arrhythmia and reducing the occurrence of ventricular fibrillation from 75% to 25%. Liriodendrin has inhibitory activities on gastritis and gastric ulcer, it can inhibit colonization of Helicobacter pylori effectively, it could be utilized for the treatment and/or protection of gastritis and gastric ulcer.
    Targets: PGE | ATPase | Potassium Channel | NO | TNF-α | NOS | COX | ROS | p53 | VEGFR | p65 | NF-kB
    In vitro:
    Arch Pharm Res. 1999 Feb;22(1):30-4.
    Metabolism of liriodendrin and syringin by human intestinal bacteria and their relation to in vitro cytotoxicity.[Pubmed: 10071956]

    METHODS AND RESULTS:
    When liriodendrin or syringin was incubated for 24 h with human intestinal bacteria, two metabolites, (+)-syringaresinol-beta-D-glucopyranoside and (+)-syringaresinol, from liriodendrin and one metabolite, synapyl alcohol, from syringin were produced. The metabolic time course of liriodendrin was as follows: at early time, liriodendrin was converted to (+)-syringaresinol-beta-D-glucopyranoside, and then (+)-syringaresinol.
    CONCLUSIONS:
    The in vitro cytotoxicities of these metabolites, (+)-syringaresinol and synapyl alcohol, were superior to those of liriodendrin and syringin.
    In vivo:
    Biomol Ther (Seoul). 2015 Jan;23(1):53-9.
    Protective Effect of Liriodendrin Isolated from Kalopanax pictus against Gastric Injury.[Pubmed: 25593644]
    In this study, we investigated the inhibitory activities on gastritis and gastric ulcer using liriodendrin which is a constituent isolated from Kalopanax pictus.
    METHODS AND RESULTS:
    To elucidate its abilities to prevent gastric injury, we measured the quantity of prostaglandin E2 (PGE2) as the protective factor, and we assessed inhibition of activities related to excessive gastric acid be notorious for aggressive factor and inhibition of Helicobacter pylori (H. pylori) colonization known as a cause of chronic gastritis, gastric ulcer, and gastric cancer. Liriodendrin exhibited higher PGE2 level than rebamipide used as a positive control group at the dose of 500 μM. It was also exhibited acid-neutralizing capacity (10.3%) and H(+)/K(+)-ATPase inhibition of 42.6% (500 μM). In pylorus-ligated rats, liriodendrin showed lower volume of gastric juice (4.38 ± 2.14 ml), slightly higher pH (1.53 ± 0.41), and smaller total acid output (0.47 ± 0.3 mEq/4 hrs) than the control group. Furthermore liriodendrin inhibited colonization of H. pylori effectively. In vivo test, liriodendrin significantly inhibited both of HCl/EtOH-induced gastritis (46.9 %) and indomethacin-induced gastric ulcer (46.1%).
    CONCLUSIONS:
    From these results, we suggest that liriodendrin could be utilized for the treatment and/or protection of gastritis and gastric ulcer.
    Arch Pharm Res. 2010 Dec;33(12):1927-32.
    A new triterpene and an antiarrhythmic liriodendrin from Pittosporum brevicalyx.[Pubmed: 21191756]
    A new triterpene, 21-O-senecioyl-R(1)-barrigenol (1) and 13 known compounds were isolated from the ethanol extracts of the leaves and bark of Pittosporum brevicalyx (Oliv.) Gagnep.
    METHODS AND RESULTS:
    Their structures were elucidated based on spectral data. The antiarrhythmic action of one furofuran lignan, liriodendrin (2), was tested on a model of CaCl(2)-induced arrhythmia and compared with the effect of verapamil. The prophylactic administration of liriodendrin (2) was effective in prolonging latency of arrhythmia and reducing the occurrence of ventricular fibrillation from 75% to 25%. The overall mortality rate was significantly reduced by the prophylactic administration of liriodendrin from 87.5% to 25%. The antiarrhythmic effect of liriodendrin (5.0 mg/kg) was similar to that of verapamil (1.05 mg/kg).
    CONCLUSIONS:
    Thus, liriodendrin may be a potent suppressor of CaCl(2)-induced arrhythmias.
    Medical Journal of Wuhan University, 2008, 29(6):759-62.
    Hypoglycemic Effects of Active Constituents Extracted from the Stem Bark of Kalopanax Septemlobus(Thunb.)Koidz.in Guangxi.[Reference: WebLink]
    To study the hypoglycemic active fractions or constituents that were extracted and isolated from the stem bark of Kalopanax septemlobus(Thunb.) Koidz.in Guangxi.
    METHODS AND RESULTS:
    Three fractions were obtained by extracting with alcohol,separating systematically and isolating by the silica and macroporous resin chromatography methods.The hypoglycemic activity of the constituents from the three fractions respectively was evaluated using diabetic models induced by alloxanin in mice.Then the effective fraction was separated by pharmacodynamic test and the monomer components were identified from the effective fraction. Three monomer components,Liriodendrin(Ⅰ),Kalopanax saponine B(Ⅱ) and Kalopanax saponine H(Ⅲ),were obtained from the only effective fraction of all the three fractions.
    CONCLUSIONS:
    Liriodendrin(Ⅰ) is thought to be found firstly in this plant,and the fraction extracted from Kalopanax septemlobus(Thunb.) Koidz.in Guangxi showes an excellent hypoglycemic activity.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.3464 mL 6.7322 mL 13.4644 mL 26.9288 mL 33.661 mL
    5 mM 0.2693 mL 1.3464 mL 2.6929 mL 5.3858 mL 6.7322 mL
    10 mM 0.1346 mL 0.6732 mL 1.3464 mL 2.6929 mL 3.3661 mL
    50 mM 0.0269 mL 0.1346 mL 0.2693 mL 0.5386 mL 0.6732 mL
    100 mM 0.0135 mL 0.0673 mL 0.1346 mL 0.2693 mL 0.3366 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
    De-4'-O-methylyangambin; De-4'-O-methylyangambin CFN99618 149250-48-6 C23H28O8 = 432.5 5mg QQ客服:3257982914
    鹅掌楸树脂醇 A ; Episyringaresinol CFN96717 51152-20-6 C22H26O8 = 418.44 5mg QQ客服:2056216494
    DL-丁香树脂酚; DL-Syringaresinol CFN99276 1177-14-6 C22H26O8 = 418.4 5mg QQ客服:1457312923
    丁香树脂酚; Syringaresinol CFN92060 487-35-4 C22H26O8 = 418.4 10mg QQ客服:1457312923
    二乙酸丁香树脂醇酯; Syringaresinol diacetate CFN98009 1990-77-8 C26H30O10 = 502.5 5mg QQ客服:215959384
    刺五加甙E1; Acanthoside B CFN97220 7374-79-0 C28H36O13 = 580.6 20mg QQ客服:2056216494
    (-)-丁香树脂醇二葡萄糖甙; 丁香树脂醇双葡萄糖苷; Syringaresinol-di-O-glucoside CFN90458 66791-77-3 C34H46O18 = 742.71 20mg QQ客服:215959384
    鹅掌楸苦素; Liriodendrin CFN98964 573-44-4 C34H46O18 = 742.7 5mg QQ客服:3257982914

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