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  • 槲皮素 3,7-双葡萄糖苷

    Quercetin 3,7-diglucoside

    槲皮素 3,7-双葡萄糖苷
    产品编号 CFN95408
    CAS编号 6892-74-6
    分子式 = 分子量 C27H30O17 = 626.5
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Flavonoids
    植物来源 The seeds of Desurainia sophia
    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
    槲皮素 3,7-双葡萄糖苷 CFN95408 6892-74-6 1mg QQ客服:3257982914
    槲皮素 3,7-双葡萄糖苷 CFN95408 6892-74-6 5mg QQ客服:3257982914
    槲皮素 3,7-双葡萄糖苷 CFN95408 6892-74-6 10mg QQ客服:3257982914
    槲皮素 3,7-双葡萄糖苷 CFN95408 6892-74-6 20mg 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
  • Wageningen University (Netherlands)
  • MTT Agrifood Research Finland (Finland)
  • Universidad de Ciencias y Artes de Chiapas (Mexico)
  • Gyeongsang National University (Korea)
  • University of the Basque Country (Spain)
  • Utrecht University (Netherlands)
  • University of Canterbury (New Zealand)
  • National Hellenic Research Foundation (Greece)
  • University of Vienna (Austria)
  • University of South Australia (Australia)
  • Universidad Industrial de Santander (Colombia)
  • Medizinische Universit?t Wien (Austria)
  • Uniwersytet Jagielloński w Krakowie (Poland)
  • Aarhus University (Denmark)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • The Korea Journal of Herbology2019, 34(2):25-32
  • Analytical Methods2018, 10(27)
  • Biomolecules.2023, 13(2):227.
  • Front Plant Sci.2022, 12:811166.
  • Int J Pharmacol2020, 16:1-9
  • Wageningen University & Research2018, January 2018
  • Antioxidants (Basel).2020, 9(2): E119
  • Chem Biodivers.2023, 20(10):e202300741.
  • BioResources J.2020, 15(3).
  • Front Pharmacol.2017, 8:205
  • Chem Res Toxicol.2023, 36(2):213-229.
  • J Pharm Biomed Anal.2019, 164:119-127
  • J Herbmed Pharmacol.2018, 7(4):280-286
  • Korean Journal of Pharmacognosy.2020, 51(2):100-106
  • Molecules.2021, 26(2):313.
  • Phytomedicine.2022, 100:154085.
  • Foods.2021, 10(12):2929.
  • Environ Toxicol.2021, 36(9):1848-1856.
  • Br J Pharmacol.2018, 175(6):902-923
  • Pharm Biol.2022, 60(1):2040-2048.
  • Bull. Pharm. Sci., Assiut University2020, 43(2):149-155.
  • Food Res Int.2018, 106:909-919
  • ACS Nano.2024, 18(9):7267-7286.
  • ...
  • 生物活性
    Description: Quercetin 3,7-diglucoside exhibits antioxidant activity.
    In vitro:
    Physiol Mol Biol Plants . 2018 Sep;24(5):881-887.
    Impact of maturity on phenolic composition and antioxidant activity of medicinally important leaves of Ficus carica L[Pubmed: 30150862]
    Ficus carica L. is one of the oldest trees belonging to the mulberry family. It has both nutritional and medicinal benefits, as it is a source of potential bioactive compounds. Fig leaves were collected at four maturation stages, to evaluate the variation in polyphenolic compounds, antioxidant activity, and different pigments level. Polyphenols were identified using HPLC-DAD. Different pigments level, total phenolic contents, and radical scavenging activity were quantified. The HPLC analysis revealed the presence of fourteen polyphenolic compounds in the fig leaves. Quercetin-3-glucoside, caftaric acid, quercetin-3, 7-diglucoside, and coumaroyl-hexose were the major phenolic compounds. Kaempferol-3-O-sophorotrioside, cichoric acid and sinapic acid glucoside were identified for the first time. Significant quantitative changes were observed during maturation, particularly in polyphenolic compounds. There were significant changes in pigments level, total phenolic contents, and radical scavenging activity. It was observed that fig leaves are a rich source of polyphenolic compounds during all stages of maturation.
    J Sci Food Agric . 2019 Feb;99(3):1046-1054.
    Preliminary evaluation of quince (Cydonia oblonga Mill.) fruit as extraction source of antioxidant phytoconstituents for nutraceutical and functional food applications[Pubmed: 30014572]
    Background: Quince (Cydonia oblonga) fruits can be considered as starting material for the extraction of health-promoting phytochemicals, to be exploited in food and nutraceuticals. In the present work, liquid chromatography coupled with diode array detection and tandem mass spectrometry analysis allowed the study of the phytochemical composition of quince fruits and to compare it with those of six commercial apple varieties. Results: The distribution and quantification of secondary metabolites in peel and pulp were studied and compared with six commercial apple varieties. Furthermore the in vitro antioxidant activity was determined by 2,2-diphenyl-2-picrylhydrazyl (DPPH) assay. Quince fruit presented significant amounts of shikimic and quinic acid derivatives, as well as flavonoids and procyanidins. Compared with apple, quince fruit composition was characterized by the presence of 4-caffeoylshikimic acid, 4-caffeoyl quinic acid, quercetin-3,7-diglucoside, kaempferol-3-O-rhamnoside and kaempferol-7-O-glucoside, and the dihydrochalcones were not detectable. The peel showed the highest contents of phenolics, whereas 3-O-caffeoylquinic acid was the most abundant compound in the quince pulp. The Pearson correlation index was calculated considering the quantitative amount of the phenolic constituents and the radical scavenging activity toward DPPH both for peel and pulp extracts. · Conclusions: This study highlighted the presence of significant amounts of valuable secondary metabolites in quince fruit, in particular the procyanidins and caffeoyl esters with shikimic and quinic acid. Notably, owing to the higher content in phenolic compounds and the stronger antioxidant capacity compared with the other fruits considered, the use of C. oblonga as a source of antioxidant can be valuable in nutraceuticals, revealing new possible applications of quince fruit. © 2018 Society of Chemical Industry.
    In vivo:
    Food Funct . 2017 Jan 25;8(1):429-436.
    Protective effects of dietary glycine and glutamic acid toward the toxic effects of oxidized mustard oil in rabbits[Pubmed: 28091680]
    The protective role of glycine and glutamic acid against the toxic effects of oxidized oil was studied for the first time. Mustard seed oil was thermally oxidized and characterized for quality characteristics and polyphenolic composition using reversed phase HPLC-DAD. Significant changes in the quality characteristics occurred with thermal oxidation. Fourteen polyphenolic compounds were identified and quantified in oils. Quercetin-3-glucoside, quercetin-3-feruloylsophoroside, catechin, quercetin-3-rutinoside, quercetin-3,7-diglucoside, sinapic acid and vanillic acid hexoside were the major compounds in the fresh and oxidized oil. Oxidized, un-oxidized mustard oils, glycine and glutamic acid were given to rabbits alone or in combination. The biochemical responses were studied in terms of haematological and biochemical parameters and histopathology. It has been observed that biochemical and haematological parameters were adversely affected by the oxidized oil, while supplementation of both amino acids was beneficial in normalizing these parameters. Both amino acids alone have no significant effects, however, oxidized oil affected the liver by enhancing fat accumulation, causing hepatitis, reactive Kupffer cells and necrosis. The co-administration of oxidized oils with glycine or glutamic acid revealed significant recovery of the liver structure and function. In conclusion, glycine or glutamic acid is beneficial and protective against food toxicity and can be considered as an ameliorative food supplement.
    J Chem Ecol . 1987 Mar;13(3):473-493.
    Flavonoid pigments in chalkhill blue (Lysandra coridon Poda) and other lycaenid butterflies[Pubmed: 24301889]
    Nine flavonoids, namely, kaempferol, kaempferol 7-rharanoside, kaempferol 3-rhamnoside, kaempferol 3-glucoside, kaempferol 3-glucoside, 7-rhamnoside, quercetin 3-glucoside, quercetin 3,7-diglucoside, isorhamnetin 3-glucoside, and isorhamnetin 3,7-diglucoside, have been identified in the body and wings of the chalkhill blue butterflyLysandra coridon Poda. Flavonoids have also been found in 15 of a further 17 lycaenid species examined. Analysis of the two-dimensional paper chromatographic flavonoid patterns and aglycone results has shown that the flavonoid content ofL. coridon and the other lycaenids is dependent on the flavonoid content of the larval diet. Differences in the flavonoid patterns ofL. coridon and its leguminous larval food plantsHippocrepis comosa, Anthyllis vulneraria, andLotus corniculatus, indicate that the ingested flavonoids are metabolized byL. coridon or its gut flora before sequestration. Despite the presence of fiavones, glycoflavones, and isoflavones in the larval food plant species, only flavonols are sequestered by the lycaenid species examined. The relationship between lycaenid butterflies and their larval food plants, and the possible role(s) of flavonoids in lycaenids has been discussed. Interactions between ants, plants, flavonoids, and myrmecophilous lycaenids have also been considered.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.5962 mL 7.9808 mL 15.9617 mL 31.9234 mL 39.9042 mL
    5 mM 0.3192 mL 1.5962 mL 3.1923 mL 6.3847 mL 7.9808 mL
    10 mM 0.1596 mL 0.7981 mL 1.5962 mL 3.1923 mL 3.9904 mL
    50 mM 0.0319 mL 0.1596 mL 0.3192 mL 0.6385 mL 0.7981 mL
    100 mM 0.016 mL 0.0798 mL 0.1596 mL 0.3192 mL 0.399 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
    Durantoside I; Durantoside I CFN97726 53526-67-3 C26H32O13 = 552.53 5mg QQ客服:3257982914
    14-去氧穿心莲内酯; 14-Deoxyandrographolide CFN92802 4176-97-0 C20H30O4 = 334.45 10mg QQ客服:1413575084
    Oplodiol; Oplodiol CFN99440 13902-62-0 C15H26O2 = 238.4 5mg QQ客服:2056216494
    Carasinol B; Carasinol B CFN95042 777857-86-0 C56H44O13 = 925.0 5mg QQ客服:2159513211

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