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  • Meloside A

    Meloside A

    Meloside A
    产品编号 CFN90132
    CAS编号 60767-80-8
    分子式 = 分子量 C27H30O15 = 594.52
    产品纯度 >=98%
    物理属性 Yellow powder
    化合物类型 Flavonoids
    植物来源 The leaves of Cucumis sativus
    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
    Meloside A CFN90132 60767-80-8 1mg QQ客服:1457312923
    Meloside A CFN90132 60767-80-8 5mg QQ客服:1457312923
    Meloside A CFN90132 60767-80-8 10mg QQ客服:1457312923
    Meloside A CFN90132 60767-80-8 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
    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
  • Griffith University (Australia)
  • The Ohio State University (USA)
  • Leibniz-Institut für Pflanzenbiochemie (IPB) (Germany)
  • National Chung Hsing University (Taiwan)
  • Universit?t Basel (Switzerland)
  • Sant Gadge Baba Amravati University (India)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Research Square2021, 10.21203.
  • J Cell Biochem.2022, 123(7):1222-1236.
  • BMC Complement Altern Med.2019, 19(1):325
  • J of l. Chroma.&Related Tech2020, 43(11-12):414-423.
  • Asian Journal of Chemistry2014, 26(22):7811-7816
  • Chin. Med.J.Res. Prac.2017, 31(4)
  • Daru.2022, 30(2):273-288.
  • Molecules.2022, 27(4):1412.
  • J Nat Med.2021, doi: 10.1007.
  • Pharmacognosy Journal2019, 11(2): 369-373
  • Virus Res.2023, 335:199199.
  • Int J Mol Sci.2024, 25(2):764.
  • Appl Microbiol Biotechnol.2018, 102(12):5105-5120
  • The Catharanthus Genome2022,35-83.
  • Aging (Albany NY).2023, 15(24):15557-15577.
  • Applied Physics B2021, 127(92).
  • Regul Toxicol Pharmacol.2024, 149:105620.
  • Auburn University2015, 1-58
  • Molecules.2022, 27(21):7514.
  • Appl. Sci. 2021, 11(8),3437.
  • Molecules 2021, 26(4),1092.
  • J Drug Delivery Science and Tech.2022, 67:102957.
  • Cells.2022, 11(8), 1311.
  • ...
  • 生物活性
    Description: Reference standards.
    In vitro:
    Plant Sci . 2013 Sep;210:61-9.
    Metabolite profiling of the short-term responses of rice leaves (Oryza sativa cv. Ilmi) cultivated under different LED lights and its correlations with antioxidant activities[Pubmed: 23849114]
    Abstract Metabolite profiling of rice leaves (Oryza sativa cv. Ilmi) was performed to investigate the short-term responses to different light-emitting diode (LED) lights, blue (B), green (G), red (R), white (W), shade (S), by using gas chromatography-ion trap-mass spectrometry (GC-IT-MS) and ultra-performance liquid chromatography-quadrupole-time-of-flight-mass spectrometry (UPLC-Q-TOF-MS) with multivariate analysis. Clear grouping patterns of each light-grown sample, except G and W, were shown in partial least squares-discriminant analysis (PLS-DA). Thirty-two primary metabolites and eleven secondary metabolites were selected and visualized using heatmap. Antioxidant activities of rice leaves followed the order B=W=G>R>S and isoorientin-2''-O-glucoside, isovitexin-2''-O-glucoside, isoorientin-2''-O-(6'''-ρ-coumaroyl)-glucoside, and isoscoparin-2''-O-glucoside showed similar relative differences and had higher Pearson's correlation coefficients than other metabolites in correlation network. According to the orthogonal projection to latent structures-discriminant analysis (OPLS-DA) between B and R, the levels of amino acids, organic acids, fatty acids, and flavonoid glycosides were relatively high in B, whereas the glucose and fructose levels were high in R. Keywords: Antioxidant activity; GC–IT-MS; LED lights; Metabolite profiling; Oryza sativa; UPLC–Q-TOF-MS.
    Phytochemistry . 2018 Apr;148:11-20.
    Changes in isovitexin-O-glycosylation during the development of young barley plants[Pubmed: 29421507]
    Abstract Phenylpropanoids are a class of plant natural products that have many biological functions, including stress defence. In barley, phenylpropanoids have been described as having protective properties against excess UV-B radiation and have been linked to resistance to pathogens. Although the phenylpropanoid composition of barley has recently been addressed in more detail, the biosynthesis and regulation of this pathway have not been fully established. Barley introgression lines, such as the S42IL-population offer a set of genetically diverse plants that enable the correlation of metabolic data to distinct genetic regions on the barley genome and, subsequently, identification of relevant genes. The phenylpropanoid profiles of the first and third leaf of barley seedlings in Scarlett and four members of the S42IL-population were obtained by LC-MS. Comparison of the leaf profiles revealed a change in the glycosylation pattern of the flavone-6-C-glucoside isovitexin in the elite cultivar Scarlett. The change was characterized by the stepwise decrease in isovitexin-7-O-glucoside (saponarin) and an increase in isovitexin-2″-O-β-D-glucoside content. The lines S42IL-101-, -177 and -178 were completely devoid of isovitexin-2″-O-β-D-glucoside. Parallel glucosyltransferase assays were consistent with the observed metabolic patterns. The genetic region responsible for this metabolic effect was located on chromosome 1H between 0.21 and 15.08 cM, encompassing 505 gene candidates in the genome of the sequenced cultivar Morex. Only one of these genes displayed sequence similarity with glucosyltransferases of plant secondary metabolism that possessed the characteristic PSPG motif. Keywords: 441381); Barley introgression lines; Flavonoids; Hordeum vulgare spp. vulgare; Isovitexin-2″-O-β-D-glucoside; Isovitexin-2″-O-β-D-glucoside (PubChem CID: 25202838); Isovitexin-7-O-glucoside; Isovitexin-7-O-glucoside (PubChem CID:; LC-MS; Metabolite profiling; Morex; Phenylpropanoids; Poaceae; Scarlett.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.682 mL 8.4101 mL 16.8203 mL 33.6406 mL 42.0507 mL
    5 mM 0.3364 mL 1.682 mL 3.3641 mL 6.7281 mL 8.4101 mL
    10 mM 0.1682 mL 0.841 mL 1.682 mL 3.3641 mL 4.2051 mL
    50 mM 0.0336 mL 0.1682 mL 0.3364 mL 0.6728 mL 0.841 mL
    100 mM 0.0168 mL 0.0841 mL 0.1682 mL 0.3364 mL 0.4205 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
    Margaritene; Margaritene CFN95303 64271-10-9 C28H32O14 = 592.6 10mg QQ客服:1457312923
    砂生槐黄酮 A; Sophoraflavone A CFN95510 105594-08-9 C27H30O13 = 562.5 10mg QQ客服:215959384
    牡荆素-2''-O-鼠李糖苷; Vitexin-2''-O-rhamnoside CFN98177 64820-99-1 C27H30O14 = 578.52 20mg QQ客服:2056216494
    牡荆素-2''-O-葡萄糖苷; Vitexin 2''-glucoside CFN70421 61360-94-9 C27H30O15 = 594.5 5mg QQ客服:3257982914
    牡荆素 2''-O-(4'''-O-乙酰)鼠李糖苷; Vitexin 2''-O-(4'''-O-acetyl)rhamnoside CFN96447 80537-98-0 C29H32O15 = 620.56 5mg QQ客服:1413575084
    牡荆素-4''-O-葡萄糖苷; Vitexin -4''-O-glucoside CFN92072 178468-00-3 C27H30O15 = 594.5 20mg QQ客服:3257982914
    异斯皮诺素; Isospinosin CFN95350 89701-83-7 C28H32O15 = 608.6 5mg QQ客服:2159513211
    芹菜素-6-C-α-L-阿拉伯糖-8-C-β-D-木糖苷; Apigenin 6-C-alpha-L-arabinopyranosyl-8-C-beta-D-xylopyranoside CFN90918 677021-30-6 C25H26O13 = 534.47 5mg QQ客服:1413575084
    芹菜素-6,8-二-C-α-L-吡喃阿拉伯糖苷; Apigenin 6,8-di-C-alpha-L-arabinopyranoside CFN95360 73140-47-3 C25H26O13 = 534.5 10mg QQ客服:2056216494
    维采宁-3; Vicenin -3 CFN92032 59914-91-9 C26H28O14 = 564.5 20mg QQ客服:1413575084

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