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  • 金丝桃素

    Hypericin

    金丝桃素
    产品编号 CFN99188
    CAS编号 548-04-9
    分子式 = 分子量 C30H16O8 = 504.45
    产品纯度 >=98%
    物理属性 Yellow powder
    化合物类型 Anthraquinones
    植物来源 The herbs of Hypericum perforatum L.
    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
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    金丝桃素 CFN99188 548-04-9 10mg QQ客服:3257982914
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    金丝桃素 CFN99188 548-04-9 100mg QQ客服:3257982914
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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
  • Srinakharinwirot University (Thailand)
  • Michigan State University (USA)
  • University of Canterbury (New Zealand)
  • University of Malaya (Malaysia)
  • National Cancer Center Research Institute (Japan)
  • Institute of Pathophysiology Medical University of Vienna (Austria)
  • University of Pretoria (South Africa)
  • Institute of Bioorganic Chemistry Polish Academy of Sciences (Poland)
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  • University of Toulouse (France)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Saudi Pharm J.2019, 27(1):145-153
  • J Nutr Biochem.2022, 107:109064.
  • Asian J of Pharmaceutical&Clinical 2018, 11(2)
  • J Sep Sci.2018, 41(7):1682-1690
  • Food Chem.2019, 290:286-294
  • Separations2023, 10(2), 131.
  • Jour. of Stored Pro & Postharvest Res.2016, 7(3):32-36
  • J Nat Sc Biol Med2019, 10(2):149-156
  • Antioxidants (Basel).2022, 11(8):1471.
  • Molecules.2021, 26(3):695.
  • Int J Mol Sci.2023, 24(17):13230.
  • Biomed Pharmacother.2022, 145:112410.
  • Chinese Medicine2019, 14(1)
  • Mol Med Rep.2022, 25(1):8.
  • Plant Growth Regulation2020, 90(2):383-392
  • J Nat Med.2020, 74(1):65-75
  • Environ Toxicol.2019, 34(12):1354-1362
  • Phytomedicine.2019, 61:152813
  • Anal Sci.2019, 35(12):1317-1325
  • Research on Crops.2017, 18(2)
  • Chemistry of Plant Raw Materials2022, 20220210569.
  • Nutrients.2019, 12(1):E40
  • Comparative Clinical Pathology 2021, 30:961-971.
  • ...
  • 生物活性
    Description: Hypericin is a photosensitive antiviral with anticancer and antidepressant agent . It can inhibit tyrosine kinases with IC50 of 7.5 μM. It can induce both apoptosis and necrosis in a concentration and light dose-dependent fashion, and inhibit RANKL-mediated osteoclastogenesis via affecting ERK signalling in vitro and suppresses wear particle-induced osteolysis in vivo.
    Targets: PKC | ERK | NF-kB | JNK | p38MAPK
    In vitro:
    Int J Biochem Cell Biol. 2002 Mar;34(3):221-41.
    Hypericin in cancer treatment: more light on the way.[Pubmed: 11849990]
    Photodynamic therapy (PDT) has been described as a promising new modality for the treatment of cancer. PDT involves the combination of a photosensitizing agent (photosensitizer), which is preferentially taken up and retained by tumor cells, and visible light of a wavelength matching the absorption spectrum of the drug. Each of these factors is harmless by itself, but when combined they ultimately produce, in the presence of oxygen, cytotoxic products that cause irreversible cellular damage and tumor destruction. Hypericin, a powerful naturally occurring photosensitizer, is found in Hypericum perforatum plants, commonly known as St. John's wort. In recent years increased interest in hypericin as a potential clinical anticancer agent has arisen since several studies established its powerful in vivo and in vitro antineoplastic activity upon irradiation. Investigations of the molecular mechanisms underlying hypericin photocytotoxicity in cancer cells have revealed that this photosensitizer can induce both apoptosis and necrosis in a concentration and light dose-dependent fashion. Moreover, PDT with hypericin results in the activation of multiple pathways that can either promote or counteract the cell death program. This review focuses on the more recent advances in the use of hypericin as a photodynamic agent and discusses the current knowledge on the signaling pathways underlying its photocytotoxic action.
    J BUON. 2014 Jul-Sep;19(3):627-32.
    The effects of hypericin on ADAMTS and p53 gene expression in MCF-7 breast cancer cells.[Pubmed: 25261644]
    The purpose of this study was to determine the effects of hypericin on MCF-7 (Michigan Cancer Foundation- 7) breast cancer cells, as it is known to exert an antitumor effect on the expression and regulation of ADAMTS1, 3, 10 and the p53 gene in breast cancer cells.
    METHODS AND RESULTS:
    MFC-7 cells were cultured and subjected separately to various doses (1, 5 and 7.5 μg /mL) hypericin. After 24 hrs, RNA was isolated and transcribed into cDNA. Expression analysis was performed by real time (RT)-PCR and cell survival was determined by the XTT assay. While the expression of ADAMTS1 in MFC-7 cells decreased to 0.04-fold after exposure to 1 μg /mL hypericin, the expression increased by 5.6- and 36-fold with 5 and 7.5 μg/mL, respectively. Furthermore, ADAMTS3 expression in MCF7 cells increased 3.9-fold with the use of 5 μg /mL of hypericin. These concentrations of hypericin did not lead to significant changes in the expression of ADAMTS10 and the p53 gene. Viability of cancer cells as evaluated by the XTT assay showed that hypericin concentration of 7.5 μg /mL led to increased apoptosis of cancer cells.
    CONCLUSIONS:
    The increase in ADAMTS1 expression may prevent metastasis or facilitate the development of an adjuvant factor with tumor-suppressive effects. Hypericin may therefore exert its antitumor and apoptotic effects in MFC-7 cells via ADAMTS1 and ADAMTS3.
    Biochem. Biophys. Res. Commun., 1989 ,165(3):1207-12.
    Hypericin and pseudohypericin specifically inhibit protein kinase C: Possible relation to their antiretroviral activity[Pubmed: 2558652]
    Hypericin and pseudohypericin which have been isolated from plants of the Hypericum family are aromatic polycyclic diones. Daniel Meruelo et. al. have reported that hypericin and pseudohypericin showed potent antiretroviral activity including anti-human immunodeficiency virus (1,2). However, the mechanism of these antiretroviral activities has not been clarified.
    METHODS AND RESULTS:
    In the course of screening specific inhibitors of protein kinase C we have found that both compounds specifically inhibit protein kinase C with IC50 values 1.7 micrograms/ml and 15 micrograms/ml, respectively, and show antiproliferative activity against mammalian cells.
    CONCLUSIONS:
    These data suggest that antiretroviral activity of hypericin and pseudohypericin could be attributable to the inhibition of some phosphorylation involved by protein kinase C during viral infection of cells.
    In vivo:
    Planta Med. 1998 May;64(4):291-4.
    Solubilized hypericin and pseudohypericin from Hypericum perforatum exert antidepressant activity in the forced swimming test.[Pubmed: 9619107]

    METHODS AND RESULTS:
    It has been shown recently that the fraction IIIc of a crude extract of Hypericum perforatum, (St. John's wort) that contained both hypericin (1) and pseudohypericin (2), was remarkably active in the rats forced swimming test (FST) after Porsolt. However, neither of the naphthodianthrones isolated from this fraction were sufficiently effective when administered suspended in water. The solubility of 1 and 2 is remarkably increased in the presence of a fraction containing procyanidins, especially procyanidin B2, which is present also in the active Hypericum fraction IIIc. The cooperative effect of procyanidins significantly increased the in vivo effects of 1 and 2, which exhibited inverted U-shaped dose response curves, in the FST. The anti-immobility effect of solubilized 1 and 2 was antagonized by the dopamine antagonist sulpiride.
    CONCLUSIONS:
    These data indicate that naphthodianthrones are antidepressant constituents of H. perforatum and suggest that the dopaminergic system is involved in their action.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.9824 mL 9.9118 mL 19.8236 mL 39.6471 mL 49.5589 mL
    5 mM 0.3965 mL 1.9824 mL 3.9647 mL 7.9294 mL 9.9118 mL
    10 mM 0.1982 mL 0.9912 mL 1.9824 mL 3.9647 mL 4.9559 mL
    50 mM 0.0396 mL 0.1982 mL 0.3965 mL 0.7929 mL 0.9912 mL
    100 mM 0.0198 mL 0.0991 mL 0.1982 mL 0.3965 mL 0.4956 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
    原伪金丝桃素; Protopseudohypericin CFN90677 54328-09-5 C30H18O9 = 522.46 10mg QQ客服:2159513211
    番泻苷元A; Sennidin A CFN99597 641-12-3 C30H18O10 = 538.46 5mg QQ客服:215959384
    番泻苷元B; Sennidin B CFN99598 517-44-2 C30H18O10 = 538.46 5mg QQ客服:1413575084
    番泻苷A; Sennoside A CFN99903 81-27-6 C42H38O20 = 862.74 20mg QQ客服:215959384
    番泻苷B; Sennoside B CFN99904 128-57-4 C42H38O20 = 862.74 20mg QQ客服:1457312923
    番泻苷C; Sennoside C CFN99905 37271-16-2 C42H40O19 = 848.76 10mg QQ客服:2159513211
    番泻苷D; Sennoside D CFN99906 37271-17-3 C42H40O19 = 848.76 5mg QQ客服:2159513211
    1,5,7'-联大黄素甲醚; Floribundone 1 CFN97845 118555-84-3 C32H22O10 = 566.52 5mg QQ客服:215959384
    原金丝桃素; Protohypericin CFN93055 548-03-8 C30H18O8 = 506.46 5mg QQ客服:2056216494
    金丝桃素; Hypericin CFN99188 548-04-9 C30H16O8 = 504.45 20mg QQ客服:1457312923

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