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  • 堪非醇3-O-阿拉伯糖苷

    Kaempferol 3-O-arabinoside

    堪非醇3-O-阿拉伯糖苷
    产品编号 CFN97572
    CAS编号 99882-10-7
    分子式 = 分子量 C20H18O10 = 418.4
    产品纯度 >=98%
    物理属性 Yellow powder
    化合物类型 Flavonoids
    植物来源 The roots of Ligusticum jeholense Nakai et Kitag.
    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
    堪非醇3-O-阿拉伯糖苷 CFN97572 99882-10-7 1mg QQ客服:215959384
    堪非醇3-O-阿拉伯糖苷 CFN97572 99882-10-7 5mg QQ客服:215959384
    堪非醇3-O-阿拉伯糖苷 CFN97572 99882-10-7 10mg QQ客服:215959384
    堪非醇3-O-阿拉伯糖苷 CFN97572 99882-10-7 20mg QQ客服:215959384
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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 Minnesota (USA)
  • National Research Council of Canada (Canada)
  • Northeast Normal University Changchun (China)
  • Aveiro University (Portugal)
  • University of Otago (New Zealand)
  • University of Cincinnati (USA)
  • Srinakharinwirot University (Thailand)
  • Univerzita Karlova v Praze (Czech Republic)
  • Universidad de Ciencias y Artes de Chiapas (Mexico)
  • Heinrich-Heine-University Düsseldorf (Germany)
  • Biotech R&D Institute (USA)
  • Julius Kühn-Institut (Germany)
  • Cancer Research Initatives Foundation(CARIF) (Malaysia)
  • University of Maryland (USA)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Nat Prod Commun.2017, 12(5):771-778
  • Kor. J. Herbol.2019, 34(2):59-66
  • Phytomedicine.2024, 155760.
  • J Mater Chem B.2019, 7(39):5896-5919
  • Molecular & Cellular Toxicology 2024, 00444-8.
  • Pharmaceuticals (Basel).2021, 14(8):742.
  • Korean Journal of Pharmacognosy2017, 48(4):320-328
  • Sci Rep.2023, 13(1):7475.
  • Inflammation.2022, 45(6):2529-2543.
  • Int J Nanomedicine.2024, 19:1683-1697.
  • Journal of Life Science2018, 917-922
  • Planta Med.2019, 85(4):347-355
  • Food Bioscience2023, 56:103311.
  • Agronomy 2021, 11(3),502.
  • Int J Mol Sci.2020, 21(7):2530.
  • Front Chem.2022, 10:1048467.
  • J Vet Sci.2020, 21(3):e39.
  • The Japan Society for Analytical Chemistry2018, 67(4):201-206
  • Molecules.2019, 24(4):E709
  • Biomedicines.2022, 10(5):1170
  • J Appl Biol Chem.2022, 65(4):pp.463-469.
  • Korea Institute of Oriental Medicine2020, doi: 10.21203.
  • J Cell Biochem.2018, 119(2):2231-2239
  • ...
  • 生物活性
    Description: Kaempferol-3-O-α-D-arabinoside displays cytotoxic and high antioxidant activity.Kaempferol-3-O-arabinoside and kaempferol-3-O-glucoside can function as antioxidants in biological systems, particularly skin exposed to UV radiation by scavenging ROS, and protect cellular membrane against ROS; they can be applicable to new cosmeceuticals for antioxidant, antiaging, and antibacterial activity.
    Targets: Antifection | ROS
    In vitro:
    Food Science and Technology Research.2006 Feb;12(1):31-37.
    Identification of the Major Polyphenols in Boysenberry Leaves and Their Suppressive Effect on Carbon Tetrachloride-Induced Liver Injury in Mice.[Reference: WebLink]
    Seven polyphenols were isolated from leaves of New Zealand boysenberry.
    METHODS AND RESULTS:
    On the basis of spectroscopic analysis, the structures of these compounds were elucidated to be quercetin 3-O-glucuronide, quercetin 3-O-glucoside, quercetin 3-O-arabinoside, kaempferol 3-O-glucuronide, kaempferol 3-O-arabinoside, kaempferol 3-O-(6"-O-p-coumaroyl)-glucoside, and ellagic acid. Increases in plasma aspartate aminotrasferase and alanine aminotrasferase activities in mice, induced with liver injury by the injection of carbon tetrachloride, were suppressed by oral administration of the polyphenol fraction prepared from the leaves, with ellagic acid as its effective component.
    CONCLUSIONS:
    Thus polyphenol fraction contained in boysenberry leaves may be effective in suppressing liver injury.
    Journal of the Society of Cosmetic Scientists of Korea.2010,36(4):303-14.
    Antibacterial, Antioxidative Activity and Component Analysis of Pinus koraiensis Leaf Extracts[Reference: WebLink]

    METHODS AND RESULTS:
    In this study, the antibacterial, antioxidative effect and component analysis of Pinus koraiensis leaf extracts were investigated. MIC values of the ethyl acetate fraction from P. koraiensis leaf extracts on P. acnes, S. aureus, P. ovale, and E. coli were 0.06 %, 0.25 %, 0.13 % and 0.50 %, respectively. The results showed that the antibacterial activity of the ethyl acetate fraction on P. acnes, P. ovale. and S. aureus was more prominent. The aglycone fraction of P. koraiensis leaf extracts () showed more higher free radical (1,1-diphenyl-2-picrylhydrazyl, DPPH) scavenging activity (). Reactive oxygen species (ROS) scavenging activity () of P. koraiensis leaf extracts on ROS generated in -EDTA/ system was investigated using the luminol-dependent chemiluminescence assay. The 50 % ethanol extract () showed the most prominent ROS scavenging activity. Also the ethyl acetate () and the aglycone fraction () showed very high antoxidant activity. The protective effects of extract/fractions of P. koraiensis leaf extracts on the rose-bengal sensitized photohemolysis of human erythrocytes were investigated. The P. koraiensis leaf extracts showed cellular membrane protective effects in a concentration dependent manner (). TLC and HPLC chromatogram of the ethyl acetate fraction obtained from hydrolysis of P. koraiensis leaf extracts revealed 2 main bands (PK-4, PK-6) and peaks (peak 1, peak 2), which were identified as kaempferol-3-O-glucoside (PK-6, peak 1) and Kaempferol 3-O-arabinoside (PK-4, peak 2) by LC/ESI-MS/MS, respectively.
    CONCLUSIONS:
    These results indicate that extract/fractions of P. koraiensis can function as antioxidants in biological systems, particularly skin exposed to UV radiation by scavenging ROS, and protect cellular membrane against ROS. Extract/fractions of P. koraiensis can be applicable to new cosmeceuticals for antioxidant, antiaging, and antibacterial activity.
    Nat. Prod. J., 2013, 3: 77-80.
    Radical-Scavenging Activity, Cytotoxicity and Chemical Constituents of Euphorbia orthoclada from Madagascar.[Reference: WebLink]

    METHODS AND RESULTS:
    Both cyclohexane and ethyl acetate fractions were toxic against brine shrimp larvae (Artemia salina) at a concentration of 10 μg/mL with mortality rates of 62% and 70%, respectively; however, the ethyl acetate extract proved to have the most effective antioxidant activity with an EC50 value of 3.45 ± 0.01 μg/mL. Five phenolic compounds 1-5 were isolated from the EtOAc extract by successive chromatographic procedures (silica gel, Sephadex LH-20). Among them, quercetin-3-O-α-D-arabinoside (2) (28.5 ± 0.11 μg/mL), kaempferol-3-O-β-D-glucoside (4) (37.2 ± 0.17 μg/mL), kaempferol-3-O-α-D-arabinoside (Kaempferol 3-O-arabinoside,3) (38.4 ± 0.13 μg/mL) and gallic acid (1) (55.22 ± 0.15 μg/mL) displayed the highest antioxidant activity, while 3,3',4'-trimethylellagic acid 4-O-glucoside (5) (63.90 ± 0.09 μg/mL) was more toxic than the other constituents on brine shrimp larvae when tested at 10 μg/mL (mortality rate of 65 %).
    CONCLUSIONS:
    The medicinal plant Euphorbia orthoclada - namely its chemical constituents - has been investigated for the first time in this project. The cytotoxic and antioxidant properties of the pure secondary metabolites explain the use of this plant in traditional medicine. Moreover, the isolation of compounds 2, 3 and 4 from E. orthoclada emphasizes that these metabolites may be considered as chemotaxonomic markers of the genus Euphorbia.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.3901 mL 11.9503 mL 23.9006 mL 47.8011 mL 59.7514 mL
    5 mM 0.478 mL 2.3901 mL 4.7801 mL 9.5602 mL 11.9503 mL
    10 mM 0.239 mL 1.195 mL 2.3901 mL 4.7801 mL 5.9751 mL
    50 mM 0.0478 mL 0.239 mL 0.478 mL 0.956 mL 1.195 mL
    100 mM 0.0239 mL 0.1195 mL 0.239 mL 0.478 mL 0.5975 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
    阿福豆苷; Afzelin CFN98757 482-39-3 C21H20O10 = 432.4 20mg QQ客服:3257982914
    2'',4''-二-O-(E-对香豆酰)阿福豆甙; 2'',4''-Di-O-(E-p-coumaroyl)afzelin CFN96246 163434-73-9 C39H32O14 = 724.7 5mg QQ客服:2159513211
    2'',4''-二-O-(Z-对香豆酰)阿福豆甙; 2'',4''-Di-O-(Z-p-coumaroyl)afzelin CFN97788 205534-17-4 C39H32O14 = 724.68 5mg QQ客服:2159513211
    山奈酚3-O-半乳糖苷; Kaempferol-3-O-galactoside CFN92079 23627-87-4 C21H20O11 = 448.4 10mg QQ客服:2056216494
    山奈酚葡萄糖醛酸苷; Kaempferol-3-beta-O-glucuronide CFN90359 22688-78-4 C21H18O12 = 462.36 5mg QQ客服:2056216494
    紫云英苷; Astragalin CFN98733 480-10-4 C21H20O11 = 448.4 20mg QQ客服:1413575084
    堪非醇3-O-(6''-O-乙酰基)葡萄糖甙; 6''-O-Acetylastragalin CFN99281 118169-27-0 C23H22O12 = 490.4 5mg QQ客服:2159513211
    2''-乙酰基黄芪苷; 2''-Acetylastragalin CFN97940 1206734-95-3 C23H22O12 = 490.4 5mg QQ客服:2056216494
    山奈酚 3-O-(6''-没食子酰基)-beta-D-吡喃葡萄糖苷; Kaempferol 3-O-(6''-galloyl)-beta-D-glucopyranoside (Astragalin 6''-O-gallate) CFN92383 56317-05-6 C28H24O15 = 600.5 5mg QQ客服:1457312923
    山奈酚 3-(2''-没食子酰基葡萄糖苷); Kaempferol 3-(2''-galloylglucoside) CFN95692 76343-90-3 C28H24O15 = 600.5 5mg QQ客服:2159513211

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