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  • 7-乙基喜树碱

    7-Ethylcamptothecin

    7-乙基喜树碱
    产品编号 CFN90336
    CAS编号 78287-27-1
    分子式 = 分子量 C22H20N2O4 = 376.41
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源 The barks of Camptotheca acuminata Decne
    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
    7-乙基喜树碱 CFN90336 78287-27-1 10mg QQ客服:2056216494
    7-乙基喜树碱 CFN90336 78287-27-1 20mg QQ客服:2056216494
    7-乙基喜树碱 CFN90336 78287-27-1 50mg QQ客服:2056216494
    7-乙基喜树碱 CFN90336 78287-27-1 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
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J Neuroinflammation.2023, 20(1):268.
  • JAOCS2021, 98(7):779-794.
  • Int. J. Mol. Sci.2022, 23(14),7699;
  • Appl. Sci.2021, 11(19),9343.
  • Oncol Lett.2020, 20(4):122.
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  • iScience.2024, 4790628.
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  • Pharmaceuticals (Basel).2024, 17(3):341.
  • Plant Sci.2020, 301:110656.
  • Antioxidants (Basel).2023, 12(2):447.
  • Biomolecules.2022, 12(12):1754.
  • Cancers (Basel).2021, 13(17):4327.
  • J Food Biochem.2020, 44(6):e13198.
  • PLoS One.2021, 16(9):e0257243.
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  • Metabolites.2020, 11(1):E11.
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  • Int. J. Mol. Sci. 2022, 23(3),1696.
  • Cell Mol Biol (Noisy-le-grand).2023, 69(15):167-173.
  • ...
  • 生物活性
    Description: 7-Ethylcamptothecin has the superior antitumor activity than camptothecin, it has a stronger growth-inhibiting activity against tumor cells and remains in the intestinal tract for a longer time and in higher amounts when administered in vivo.
    In vivo:
    Cancer Treat Rep. 1987 Apr;71(4):341-8.
    Action of 7-ethylcamptothecin on tumor cells and its disposition in mice.[Pubmed: 3829011]
    Some biological effects of camptothecin (CPT) and its new derivative 7-Ethylcamptothecin (ECPT) were studied. The drugs were effective against murine leukemia; 7-Ethylcamptothecin was more effective than CPT.
    METHODS AND RESULTS:
    Ip administration of 7-Ethylcamptothecin or CPT gave maximum treated/control values of 325% and 232%, respectively. The drugs also inhibited the growth of KB cells in vitro, 50% effective doses of 3.5 ng/ml of 7-Ethylcamptothecin and 8.6 ng/ml of CPT, indicating the stronger activity of ECPT. Pharmacokinetic studies of the drugs in mice showed that 7-Ethylcamptothecin had a longer biological half-life in the terminal phase and a larger amount remained in the plasma compared with CPT. After iv administration of 7-Ethylcamptothecin, the drug accumulated in the intestine, suggesting that the main route of excretion of the drug is through the biliary tract. The study on cell cycle progression by flow cytometry suggested that the main effect of both drugs on L1210 cells was the blocking of G2-M phase.
    CONCLUSIONS:
    These results suggest that the main reasons for the superior antitumor activity of 7-Ethylcamptothecin compared with CPT are as follows: (a) 7-Ethylcamptothecin had a stronger growth-inhibiting activity against tumor cells, and (b) 7-Ethylcamptothecin remained in the intestinal tract for a longer time and in higher amounts when administered in vivo.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.6567 mL 13.2834 mL 26.5668 mL 53.1336 mL 66.4169 mL
    5 mM 0.5313 mL 2.6567 mL 5.3134 mL 10.6267 mL 13.2834 mL
    10 mM 0.2657 mL 1.3283 mL 2.6567 mL 5.3134 mL 6.6417 mL
    50 mM 0.0531 mL 0.2657 mL 0.5313 mL 1.0627 mL 1.3283 mL
    100 mM 0.0266 mL 0.1328 mL 0.2657 mL 0.5313 mL 0.6642 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
    7-乙基喜树碱; 7-Ethylcamptothecin CFN90336 78287-27-1 C22H20N2O4 = 376.41 20mg QQ客服:215959384
    7-乙基-10-羟基喜树碱; 7-Ethyl-10-Hydroxycamptothecin CFN90335 86639-52-3 C22H20N2O5 = 392.4 20mg QQ客服:1413575084
    9-甲氧基喜树碱; 9-Methoxycamptothecine CFN99729 39026-92-1 C21H18N2O5 = 378.38 20mg QQ客服:1457312923
    9-氨基喜树碱; 9-Aminocamptothecin CFN90309 91421-43-1 C20H17N3O4 = 363.37 20mg QQ客服:215959384
    (S)-10-羟基喜树碱; (S)-10-Hydroxycamptothecin CFN99735 19685-09-7 C20H16N2O5 = 364.35 20mg QQ客服:2159513211
    10-甲氧基喜树碱; 10-Methoxycamptothecin CFN90157 19685-10-0 C21H18N2O5 = 378.38 5mg QQ客服:215959384
    鲁比替康; Rubitecan CFN93013 91421-42-0 C20H15N3O6 = 393.35 5mg QQ客服:1457312923
    10-硝基喜树碱; 10-Nitro-camptothecin CFN90439 104195-61-1 C20H15N3O6 = 393.34 5mg QQ客服:1413575084
    盐酸拓扑替康; Topotecan hydrochloride CFN90462 119413-54-6 C23H24ClN3O5 = 457.9 20mg QQ客服:2056216494
    盐酸依立替康; Irinotecan hydrochloride CFN90886 100286-90-6 C33H39ClN4O6 = 623.2 20mg QQ客服:2159513211

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