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  • 9-甲氧基-alpha-拉帕醌

    9-Methoxy-alpha-lapachone

    9-甲氧基-alpha-拉帕醌
    产品编号 CFN98463
    CAS编号 35241-80-6
    分子式 = 分子量 C16H16O4 = 272.3
    产品纯度 >=98%
    物理属性 Yellow powder
    化合物类型 Quinones
    植物来源 The stems of Catalpa ovata
    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
    9-甲氧基-alpha-拉帕醌 CFN98463 35241-80-6 1mg QQ客服:1457312923
    9-甲氧基-alpha-拉帕醌 CFN98463 35241-80-6 5mg QQ客服:1457312923
    9-甲氧基-alpha-拉帕醌 CFN98463 35241-80-6 10mg QQ客服:1457312923
    9-甲氧基-alpha-拉帕醌 CFN98463 35241-80-6 20mg QQ客服:1457312923
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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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  • Universidade do Porto (Portugal)
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  • University of Illinois at Chicago (USA)
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  • National Cancer Institute (USA)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Molecules.2020, 25(23):5556.
  • J Korean Soc Food Sci Nutr2023, 52(12):1248-1255
  • Separations2021, 8(6),80.
  • Int J Mol Sci.2023, 24(17):13230.
  • Nutr Metab (Lond).2019, 16:31
  • BMC Plant Biol.2022, 22(1):128.
  • J Med Food.2021, 24(3):209-217.
  • ScientificWorldJournal.2022, 2022:4806889.
  • J Sep Sci.2019, 42(21):3352-3362
  • J Pharm Pharmacol.2023, 75(9):1225-1236.
  • Molecules2022, 27(9):2613.
  • Anat Rec (Hoboken).2021, 304(2):323-332.
  • Biol Pharm Bull.2020, 43(10):1534-1541.
  • Mol Med Rep.2024, 29(2):26.
  • Biomed Pharmacother.2024, 176:116765.
  • Fitoterapia.2015, 100:179-86
  • Int J Mol Sci.2023, 24(24):17589.
  • J Agric Food Chem.2020, 68(51):15164-15175
  • Toxins (Basel).2023, 15(3):231.
  • J Appl Biol Chem2022, 65:343−348.
  • Nutrients.2022, 14(23):4997.
  • Talanta.2023, 262:124690.
  • Aging (Albany NY).2021, 13(19):22867-22882.
  • ...
  • 生物活性
    Description: 9-Methoxy-alpha-lapachone has antitumor-promoting effect, it exhibits significant inhibitory activity against 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced Epstein- Barr virus early antigen (EBV-EA) activation in Raji cells.
    In vitro:
    Arch Pharm Res. 2010 Mar;33(3):381-5.
    Naphthoquinones from Catalpa ovata and their inhibitory effects on the production of nitric oxide.[Pubmed: 20361302]

    METHODS AND RESULTS:
    Bioassay-guided fractionation of a CH2Cl2-soluble fraction of the stems of Catalpa ovata led to isolation of a new naphthoquinone, 4-hydroxy-2-(2-methoxy-3-hydroxy-3-methyl-but-1-enyl)-4-hydro-1H-naphthalen-1-one (10), together with nine known compounds, catalponol (1), catalponone (2), catalpalactone (3), alpha-lapachone (4), 9-hydroxy-alpha-lapachone (5), 4,9-dihydroxy-alpha-lapachone (6), 9-Methoxy-alpha-lapachone (7), 4-oxo-alpha-lapachone (8), and 9-methoxy-4-oxo-alpha-lapachone (9). The structures were elucidated on the basis of spectroscopic analyses. The inhibitory effects of these isolates on lipopolysaccharide-induced NO synthesis in RAW 264.7 cells were evaluated.
    CONCLUSIONS:
    Among them, catapalactone (3), 9-hydroxy-alpha-lapachone (5) and 4,9-dihydroxy-alpha-lapachone (6) exhibited potent inhibitory effects, with IC(50) values of 9.80, 4.64 and 2.73 microM, respectively.
    J Nat Prod. 1998 May;61(5):629-32.
    Antitumor-promoting naphthoquinones from Catalpa ovata.[Pubmed: 9599262 ]

    METHODS AND RESULTS:
    Bioassay-directed fractionation of an extract of the stem-bark of Catalpa ovata led to the isolation of three new naphthoquinones: 8-methoxydehydroiso-alpha-lapachone (1), 9-methoxy-4-oxo-alpha-lapachone (2), and (4S,4aR,10R,10aR)-4, 10-dihydroxy-2,2-dimethyl-2,3,4,4alpha,10, 10alpha-hexahydrobenzo[g]chromen-5-one (3), which is a 1,4-reductive form of 6. The known compounds 3-hydroxydehydroiso-alpha-lapachone (4), 4,9-dihydroxy-alpha-lapachone (5), 4-hydroxy-alpha-lapachone (6), and 9-Methoxy-alpha-lapachone (7), and catalpalactone (8) were also isolated. Their structures were elucidated by spectral methods.
    CONCLUSIONS:
    These compounds all exhibited significant inhibitory activity against 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced Epstein-Barr virus early antigen (EBV-EA) activation in Raji cells.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.6724 mL 18.3621 mL 36.7242 mL 73.4484 mL 91.8105 mL
    5 mM 0.7345 mL 3.6724 mL 7.3448 mL 14.6897 mL 18.3621 mL
    10 mM 0.3672 mL 1.8362 mL 3.6724 mL 7.3448 mL 9.1811 mL
    50 mM 0.0734 mL 0.3672 mL 0.7345 mL 1.469 mL 1.8362 mL
    100 mM 0.0367 mL 0.1836 mL 0.3672 mL 0.7345 mL 0.9181 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
    去氢-alpha-拉杷醌; Dehydro-alpha-lapachone CFN99641 15297-92-4 C15H12O3 = 240.3 5mg QQ客服:2159513211
    alpha-拉杷醌; alpha-Lapachone CFN98702 4707-33-9 C15H14O3 = 242.3 5mg QQ客服:2056216494
    9-羟基-alpha-拉杷醌; 9-Hydroxy-alpha-lapachone CFN98215 22333-58-0 C15H14O4 = 258.3 5mg QQ客服:3257982914
    9-甲氧基-alpha-拉帕醌; 9-Methoxy-alpha-lapachone CFN98463 35241-80-6 C16H16O4 = 272.3 5mg QQ客服:1413575084
    4,9-二羟基-alpha-拉帕醌; 4,9-Dihydroxy-alpha-lapachone CFN98947 56473-67-7 C15H14O5 = 274.3 5mg QQ客服:215959384
    β-拉帕醌; Beta-Lapachone CFN91668 4707-32-8 C15H14O3 = 242.27 5mg QQ客服:1413575084

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