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  • 四氢黄连碱,人血草碱

    Tetrahydrocoptisine

    四氢黄连碱,人血草碱
    产品编号 CFN90416
    CAS编号 7461-02-1
    分子式 = 分子量 C19H17NO4 = 323.12
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源 The tubers of Corydalis yanhusuo
    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
    四氢黄连碱,人血草碱 CFN90416 7461-02-1 10mg QQ客服:2159513211
    四氢黄连碱,人血草碱 CFN90416 7461-02-1 20mg QQ客服:2159513211
    四氢黄连碱,人血草碱 CFN90416 7461-02-1 50mg QQ客服:2159513211
    四氢黄连碱,人血草碱 CFN90416 7461-02-1 100mg QQ客服:2159513211
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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)
  • Charles University in Prague (Czech Republic)
  • Universidade Católica Portuguesa (Portugal)
  • University of Leipzig (Germany)
  • Chang Gung University (Taiwan)
  • Tokyo Woman's Christian University (Japan)
  • Centralised Purchases Unit (CPU), B.I.T.S (India)
  • Warszawski Uniwersytet Medyczny (Poland)
  • Colorado State University (USA)
  • Sant Gadge Baba Amravati University (India)
  • Aarhus University (Denmark)
  • University of Malaya (Malaysia)
  • Istanbul University (Turkey)
  • 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
  • Journal of Food Composition and Analysis2021, 100:103905.
  • In Vitro Cellular & Developmental Biology - Plant2022, 58:972-988.
  • Metabolites2023, 13(1), 3.
  • Korean Journal of Medicinal Crop Science2018, 26(5):382-390
  • Fermentation2023, 9(10), 889
  • Journal of Analytical Chemistry2017, 854-861
  • Food Funct.2022, D1FO03838A.
  • Int J Mol Sci.2022, 23(11):6104.
  • Reprod Sci.2022,10.1007/s43032-022-01117-4.
  • Anticancer Res.2018, 38(4):2127-2135
  • Exp Biol Med (Maywood).2019, 244(18):1665-1679
  • Front Aging Neurosci.2019, 11:230
  • Anesth Pain Med (Seoul).2020, 15(4):478-485.
  • Food Research2021, 5(1):65-71
  • Biotechnol Bioeng.2020, 117(7):2198-2208.
  • Food Chem.2019, 290:286-294
  • J Ethnopharmacol.2019, 236:31-41
  • Front Pharmacol.2022, 13:906763.
  • Molecules.2021, 26(6):1635.
  • Int J Mol Sci.2017, 18(5)
  • Industrial Crops and Products2018, 353-362
  • Nutrients.2023, 15(6):1335.
  • Molecules.2023, 28(9):3685.
  • ...
  • 生物活性
    Description: Tetrahydrocoptisine is an active anti-inflammatory constituent by inhibition of TNF-α, IL-6 and NO production possibly via down-regulation of NF-κB activation, phospho-ERK1/2 and phospho-p38MAPK signal pathways.Tetrahydrocoptisine has gastroprotective activity, is attributed to reducing NO production and adjusting the pro-inflammatory cytokine, inhibited neutrophil accumulation and NF-κB expression.
    Targets: NF-kB | NO | TNF-α | IL Receptor | p38MAPK | ERK | p65
    In vitro:
    Yao Xue Xue Bao. 2012 Dec;47(12):1640-5.
    Synthesis and biological evaluation of tetrahydrocoptisine quaternary ammonium compounds[Pubmed: 23460970]
    The goal of treatment of metabolic syndrome is the prevention of diabetes and cardiovascular events.
    METHODS AND RESULTS:
    A series of novel tetrahydrocoptisine quaternary ammonium compounds were prepared to evaluate their action of hypoglycemia and hypolipidemia for finding the therapeutic agents of metabolic syndrome. Starting from the coptisine hydrochloride (2), fifteen target compounds were synthesized by reduction and substitution of the 7-N position. All of the target compounds were characterized by 1H NMR and HR-MS. Their hypoglycemic activities were evaluated in HepG2 cell and hypolipidemic activities of compounds with better hypoglycemic activity were tested further in vivo.
    CONCLUSIONS:
    Results indicated that compounds 5, 7, 8 and 9 exhibited better hypoglycemic activities in vitro and compounds 5 and 8 exhibited good hypolipidemic activities in high-fat-diet (HFD) induced hyperlipidemia mice and (or) hamsters. However, the activity is not as good as simvastatin.
    In vivo:
    Inflammation. 2014 Dec;37(6):2106-15.
    Tetrahydrocoptisine protects rats from LPS-induced acute lung injury.[Pubmed: 24928630]
    Recent studies show that nuclear factor-kappa B (NF-κB) signaling pathway plays a key role in contributing to the development of lipopolysaccharide (LPS)-induced acute lung injury (ALI). Tetrahydrocoptisine is one of the main active components of Chelidonium majus L. and has been described to be effective in suppressing inflammation. The aim of the present study is to evaluate the protective effect of tetrahydrocoptisine on LPS-induced ALI in rats and clarify its underlying mechanisms of action.
    METHODS AND RESULTS:
    We found that in vivo pretreatment with tetrahydrocoptisine to rats 30 min before inducing ALI by LPS markedly decreased the mortality rate, lung wet weight to dry weight ratio, and ameliorated lung pathological changes. Meanwhile, tetrahydrocoptisine significantly inhibited the increase of the amounts of inflammatory cells, total protein content, tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) secretion in the bronchoalveolar lavage fluids (BALFs). Furthermore, tetrahydrocoptisine inhibited myeloperoxidase (MPO) accumulation in lung tissue and alleviated TNF-α and IL-6 production in serum. Additionally, immunohistochemistry showed that tetrahydrocoptisine efficiently reduced nuclear factor-kappa B (NF-κB) activation by inhibiting the translocation of NF-κBp65.
    CONCLUSIONS:
    In conclusion, our results demonstrate that tetrahydrocoptisine possesses a protective effect on LPS-induced ALI through inhibiting of NF-κB signaling pathways, which may involve the inhibition of pulmonary inflammatory process.
    Eur J Pharmacol. 2013 Sep 5;715(1-3):62-71.
    Anti-inflammatory effect of tetrahydrocoptisine from Corydalis impatiens is a function of possible inhibition of TNF-α, IL-6 and NO production in lipopolysaccharide-stimulated peritoneal macrophages through inhibiting NF-κB activation and MAPK pathway.[Pubmed: 23810685]
    The extracts or constituents from Corydalis impatiens are known to have many pharmacological activities. Tetrahydrocoptisine (THC), a protoberberine compound from Corydalis impatiens, was found to possess a potent anti-inflammatory effect in different acute or chronic inflammation model animals.
    METHODS AND RESULTS:
    Pretreatment with THC (i.p.) inhibited the paw and ear edema in the carrageenan-induced paw edema assay and xylene-induced ear edema assay, respectively. In the lipopolysaccharide (LPS)-induced systemic inflammation model, THC significantly inhibited serum tumor necrosis factor-alpha (TNF-α) release in mice. To clarify its possible molecular mechanisms underlying this anti-inflammatory effect, we investigated the effect of THC on LPS-induced responses in peritoneal macrophages. Our data demonstrated that THC significantly inhibited LPS-induced TNF-α, interleukin-6(IL-6) and nitric oxide (NO) production. THC inhibited the production of TNF-α and IL-6 by down-regulating LPS-induced IL-6 and TNF-α mRNA expression. Furthermore, it attenuated the phosphorylation of p38 mitogen-activated protein kinase (p38MAPK) and phosphorylation of extracellular signal-regulated kinase1/2 (ERK1/2) as well as the expression of nuclear factor kappa B(NF-κB), in a concentration-dependent manner.
    CONCLUSIONS:
    Taken together, our data suggest that THC is an active anti-inflammatory constituent by inhibition of TNF-α, IL-6 and NO production possibly via down-regulation of NF-κB activation, phospho-ERK1/2 and phospho-p38MAPK signal pathways.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.0948 mL 15.4741 mL 30.9483 mL 61.8965 mL 77.3706 mL
    5 mM 0.619 mL 3.0948 mL 6.1897 mL 12.3793 mL 15.4741 mL
    10 mM 0.3095 mL 1.5474 mL 3.0948 mL 6.1897 mL 7.7371 mL
    50 mM 0.0619 mL 0.3095 mL 0.619 mL 1.2379 mL 1.5474 mL
    100 mM 0.0309 mL 0.1547 mL 0.3095 mL 0.619 mL 0.7737 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
    右旋四氢巴马汀; D-Tetrahydropalmatine CFN90188 3520-14-7 C21H25NO4 = 355.41 20mg QQ客服:1413575084
    四氢黄连碱,人血草碱; Tetrahydrocoptisine CFN90416 7461-02-1 C19H17NO4 = 323.12 20mg QQ客服:2159513211
    盐酸人血草碱; Stylopine hydrochloride CFN96656 96087-21-7 C19H18ClNO4 = 359.81 5mg QQ客服:1457312923
    左旋千金藤啶碱; L-Stepholidine CFN90457 16562-13-3 C19H21NO4 = 327.37 20mg QQ客服:3257982914
    (S)-金黄紫堇碱; Scoulerine CFN96330 6451-73-6 C19H21NO4 = 327.4 5mg QQ客服:2056216494
    L-四氢小檗碱; Tetrahydroberberine CFN90506 522-97-4 C20H21O4N = 339.38 20mg QQ客服:2159513211
    华紫堇碱;碎叶紫堇碱; Cheilanthifoline CFN90945 483-44-3 C19H19NO4 = 325.36 10mg QQ客服:1457312923
    四氢表小檗碱; Tetrahydroepiberberine CFN90507 38853-67-7 C20H21NO4 = 339.15 10mg QQ客服:3257982914
    延胡索单酚碱; Corypalmine CFN97021 6018-40-2 C20H23NO4 = 341.4 5mg QQ客服:2056216494
    (-)-异延胡索单酚碱; (-)-Isocorypalmine CFN90582 483-34-1 C20H23NO4 = 341.4 10mg QQ客服:2056216494

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