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  • Clivorine

    Clivorine

    Clivorine
    产品编号 CFN00355
    CAS编号 33979-15-6
    分子式 = 分子量 C21H27NO7 = 405.45
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源 The herbs of Ligularia hodgsonii Hook.
    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
    Clivorine CFN00355 33979-15-6 1mg QQ客服:2159513211
    Clivorine CFN00355 33979-15-6 5mg QQ客服:2159513211
    Clivorine CFN00355 33979-15-6 10mg QQ客服:2159513211
    Clivorine CFN00355 33979-15-6 20mg 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 Illinois (USA)
  • Subang Jaya Medical Centre (Malaysia)
  • Monash University Malaysia (Malaysia)
  • University of Wollongong (Australia)
  • Universita' Degli Studi Di Cagliari (Italy)
  • Copenhagen University (Denmark)
  • Ateneo de Manila University (Philippines)
  • University of Stirling (United Kingdom)
  • Weizmann Institute of Science (Israel)
  • John Innes Centre (United Kingdom)
  • Chinese University of Hong Kong (China)
  • Universidad Industrial de Santander (Colombia)
  • VIB Department of Plant Systems Biology, UGent (PSB) (Belgium)
  • Universit?t Basel (Switzerland)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J Biotechnol.2020, 318:10-19.
  • Molecules.2021, 26(4):816.
  • JABS2020, 14:2(2020)
  • J Korean Med Ophthalmol Otolaryngol Dermatol2023, 36(1):21-39.
  • J Ethnopharmacol.2020, 269:113752.
  • Phytomedicine.2021, 93:153796.
  • Food Chem.2019, 275:746-753
  • Chemistr of plant2016, 2016021195
  • Indian J Pharm Sci.2022, 84(4): 874-882.
  • Bioengineering2023, 10(10), 1113.
  • Molecules.2015, 20(11):20014-30
  • Chem Pharm Bull (Tokyo).2017, 65(9):826-832
  • Universitat Stuttgart2022, opus-12200.
  • J Chromatogr B Analyt Technol Biomed Life Sci. 2017, 1064:115-123
  • J of Advanced Scientific R.2020, 11(3), p109-120.
  • Chinese Pharmacological Bulletin2019, 35(8):1120-1125
  • J Biochem Mol Toxicol.2020, 34(7):e22489.
  • Research Square2021, March 3rd.
  • Int. J. of Pha. and Phy. Res.2015, 7(1):144-149
  • PLoS One.2021, 16(9):e0257243.
  • J Ethnopharmacol.2017, 206:327-336
  • Pharmaceutics.2021, 13(11):1839.
  • Biomed Pharmacother.2020, 131:110673.
  • ...
  • 生物活性
    Description: Clivorine itself has direct toxicity on HEK293 cells, and phosphorylated JNK may play some role in counteracting the toxicity of Clivorine on HEK293 cells. It has anti-proliferative function in L-02 cells may be due to its inducing cell apoptosis with independent of p53 protein. Clivorine induces hepatotoxicity and acute liver injury, which can be protected by quercetin, trolox and epidermal growth factor via inhibiting apoptotic cell death and ameliorating oxidative stress injury.
    Targets: EGFR | Caspase | JNK | ERK
    In vitro:
    Hum Exp Toxicol. 2010 Apr;29(4):303-9.
    Pyrrolizidine alkaloid clivorine induced oxidative injury on primary cultured rat hepatocytes.[Pubmed: 20144959]
    Clivorine is an otonecine-type hepatotoxic pyrrolizidine alkaloid (HPAs), to which humans are exposed when consuming herbs containing such components. In the present study, we investigated Clivorine-induced oxidative stress injury on primary cultured rat hepatocytes.
    METHODS AND RESULTS:
    Rat hepatocytes were treated with various concentrations of Clivorine (1-100 microM) for 48 hours, and then cell viability was detected by 3-(4,5-dimethyl-thiazol-2-yl) 2,5-diphenyltetrazolium bromide (MTT) assay, while lipid peroxidation (LPO) level, glutathione peroxidase (GPx), glutathione-S-transferase (GST), glutathione reductase (GR), catalase (CAT) and superoxide dismutase (SOD) activities were determined to evaluate the oxidative injury. The results of MTT assay showed that Clivorine decreased cell viability in a concentration-dependent manner. Clivorine also increased LPO amounts in rat hepatocytes at the concentrations of 50 microM and 100 microM. Further results showed that Clivorine decreased GPx, GST and GR activities, which are all reduced glutathione (GSH)-related antioxidant enzymes. CAT and SOD are both important antioxidant enzymes, and the results showed that Clivorine increased CAT activity at the low concentration of 5 muM and decreased cellular SOD activity at all concentrations.
    CONCLUSIONS:
    Taken together, our results demonstrated that Clivorine induced toxicity on primary cultured rat hepatocytes by causing the damage on cellular redox balance.
    Exp Toxicol Pathol. 2008 Jun;60(1):87-93.
    The toxic effect of pyrrolizidine alkaloid clivorine on the human embryonic kidney 293 cells and its primary mechanism.[Pubmed: 18249102]
    Clivorine is an otonecine-type pyrrolizidine alkaloid (PA) isolated from the Chinese medicinal plant Ligularia hodgsonii Hook., and our previous reports have shown its toxicity on human normal liver L-02 cells. It is generally believed that biotransformation of PAs to its metabolites is required for their toxicity; thus, there is nearly no report about the toxicity of Clivorine on other non-hepatic cells in vitro.
    METHODS AND RESULTS:
    The aim of this study is to observe the toxicity of Clivorine on the non-hepatic human embryonic kidney 293 (HEK293) cell that is of epithelial origin, and its primary mechanism. Our results showed that Clivorine significantly reduced HEK293 cell viability, but there was no detectable apoptotic DNA ladder and cleaved fragments of caspase-3 and caspase-9 in Clivorine-treated cells, which indicates the toxicity of Clivorine is not due to inducing apoptosis. The results of western blot showed that Clivorine induced sustained p38, c-Jun N-terminal kinase (JNK) and extracellular signal-related kinases (ERK1/2) phosphorylation in a concentration- and time-dependent manner, and the JNK inhibitor SP600125 significantly augmented the toxicity of Clivorine.
    CONCLUSIONS:
    Our results suggest that Clivorine itself has direct toxicity on HEK293 cells, and phosphorylated JNK may play some role in counteracting the toxicity of Clivorine on HEK293 cells.
    In vivo:
    PLoS One. 2014 Jun 6;9(6):e98970.
    Quercetin prevents pyrrolizidine alkaloid clivorine-induced liver injury in mice by elevating body defense capacity.[Pubmed: 24905073 ]
    Quercetin is a plant-derived flavonoid that is widely distributed in nature. The present study is designed to analyze the underlying mechanism in the protection of quercetin against pyrrolizidine alkaloid Clivorine-induced acute liver injury in vivo.
    METHODS AND RESULTS:
    Serum transaminases, total bilirubin analysis, and liver histological evaluation demonstrated the protection of quercetin against Clivorine-induced liver injury. Terminal dUTP nick end-labeling assay demonstrated that quercetin reduced the increased amount of liver apoptotic cells induced by Clivorine. Western-blot analysis of caspase-3 showed that quercetin inhibited the cleaved activation of caspase-3 induced by Clivorine. Results also showed that quercetin reduced the increase in liver glutathione and lipid peroxidative product malondialdehyde induced by Clivorine. Quercetin reduced the enhanced liver immunohistochemical staining for 4-hydroxynonenal induced by Clivorine. Results of the Mouse Stress and Toxicity PathwayFinder RT2 Profiler PCR Array demonstrated that the expression of genes related with oxidative or metabolic stress and heat shock was obviously altered after quercetin treatment. Some of the alterations were confirmed by real-time PCR.
    CONCLUSIONS:
    Our results demonstrated that quercetin prevents Clivorine-induced acute liver injury in vivo by inhibiting apoptotic cell death and ameliorating oxidative stress injury. This protection may be caused by the elevation of the body defense capacity induced by quercetin.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.4664 mL 12.332 mL 24.664 mL 49.3279 mL 61.6599 mL
    5 mM 0.4933 mL 2.4664 mL 4.9328 mL 9.8656 mL 12.332 mL
    10 mM 0.2466 mL 1.2332 mL 2.4664 mL 4.9328 mL 6.166 mL
    50 mM 0.0493 mL 0.2466 mL 0.4933 mL 0.9866 mL 1.2332 mL
    100 mM 0.0247 mL 0.1233 mL 0.2466 mL 0.4933 mL 0.6166 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
    18-Hydroxyspartioidine; 18-Hydroxyspartioidine CFN00478 N/A C18H23NO6 = 349.4 5mg QQ客服:3257982914
    克氏千里光碱; Senkirkine CFN00424 2318-18-5 C19H27NO6 = 365.42 5mg QQ客服:1413575084
    千里光非灵N-氧化物; Seneciphylline N-oxide CFN98618 38710-26-8 C18H23NO6 = 349.4 5mg QQ客服:2159513211
    千里光非灵; Seneciphylline CFN98747 480-81-9 C18H23NO5 = 333.4 5mg QQ客服:1413575084
    猪屎豆叶碱; Crotafoline CFN00363 38494-87-0 C18H25NO6 = 351.40 5mg QQ客服:215959384
    橐吾碱; Ligularine CFN00378 34429-54-4 C19H27NO7 = 381.4 5mg QQ客服:1413575084
    菘蓝千里光碱; Isatidine CFN00408 15503-86-3 C18H25NO7 = 367.40 5mg QQ客服:2159513211
    千里光宁氧化物; Senecionine N-oxide CFN00418 13268-67-2 C18H25NO6 = 351.17 5mg QQ客服:2056216494
    菊三七碱乙; Seneciphyllinine CFN00420 90341-45-0 C20H25NO6 = 375.42 5mg QQ客服:1413575084
    黄樟素; Riddelline CFN00421 23246-96-0 C18H23NO6 = 349.38 5mg QQ客服:2159513211

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