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  • 8-表去氧马钱子酸

    8-Epideoxyloganic acid

    8-表去氧马钱子酸
    产品编号 CFN96280
    CAS编号 88668-99-9
    分子式 = 分子量 C16H24O9 = 360.4
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Iridoids
    植物来源 The herbs of Lamiophlomis rotata.
    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
    8-表去氧马钱子酸 CFN96280 88668-99-9 10mg QQ客服:1413575084
    8-表去氧马钱子酸 CFN96280 88668-99-9 20mg QQ客服:1413575084
    8-表去氧马钱子酸 CFN96280 88668-99-9 50mg QQ客服:1413575084
    8-表去氧马钱子酸 CFN96280 88668-99-9 100mg QQ客服:1413575084
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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
  • Heinrich-Heine-University Düsseldorf (Germany)
  • Warszawski Uniwersytet Medyczny (Poland)
  • Complutense University of Madrid (Spain)
  • National Cancer Institute (USA)
  • Cornell University (USA)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Anat Rec2018, 24264
  • Front Pharmacol.2021, 12:690113.
  • Life Sci.2018, 209:498-506
  • Br J Pharmacol.2018, 175(6):902-923
  • Int J Mol Sci.2021, 22(16):8604.
  • Phytomedicine.2022, 96:153877.
  • Int J Vitam Nutr Res.2022, doi: 10.1024.
  • J Cell Mol Med.2023, 27(10):1423-1435.
  • Plant Physiol Biochem.2023, 202:107913.
  • Int J Mol Sci.2019, 20(11):E2734
  • Molecules.2019, 24(23):E4303
  • Food Chem.2019, 276:768-775
  • J Nutr Biochem.2022, 107:109064.
  • Antioxidants (Basel).2023, 13(1):12.
  • Carbohydrate Polymer Technologies & App.2021, 2:100049.
  • Metabolites.2020, 11(1):E11.
  • Molecules.2020, 25(18):4283.
  • J of Engineering Science&Technology2018, 13(9):2820-2828
  • Chem Biol Interact.2023, 378:110487.
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  • Processes2022, 10(10), 2008.
  • Front Aging Neurosci.2019, 11:230
  • Molecules.2022, 27(22):7997.
  • ...
  • 生物活性
    Description: 8-Epideoxyloganic acid possesses bioactivities of analgesia, homeostasis and anti-inflammatory. It has the potential to serve as anti-inflammatory agents during oxidative stress, the inhibition of ROS production, possibly through modulation of NOX activity and/or the radical scavenging effect, and beta2 integrin expression in leucocytes. 8-Epideoxyloganic acid (oral) shows weak antinociceptive activity.
    Targets: Immunology & Inflammation related | ROS
    In vitro:
    J Pharm Pharmacol. 2006 Jan;58(1):129-35.
    The inhibitory effect of phenylpropanoid glycosides and iridoid glucosides on free radical production and beta2 integrin expression in human leucocytes.[Pubmed: 16393473 ]
    Rapid production of reactive oxygen species (ROS) and upregulation of beta2 integrin by leucocytes are two important inflammatory responses in human leucocytes.
    METHODS AND RESULTS:
    To evaluate whether three phenylpropanoid glycosides (acteoside, crenatoside, and rossicaside B) and two iridoid glucosides (boschnaloside and 8-Epideoxyloganic acid) identified from two medicinal plants with similar indications (Orobanche caerulescens and Boschniakia rossica) exhibited anti-inflammatory activity, their effects on N-formyl-methionyl-leucyl-phenylalanine (fMLP) and phorbol-12-myristate-13-acetate (PMA)-activated peripheral human neutrophils (PMNs) and mononuclear cells were examined. Furthermore, all compounds, except rossicaside B, significantly inhibited PMA- and fMLP-induced Mac-1 (a beta2 integrin) upregulation at 50 microM but not that of fMLP-induced intracellular calcium mobilization. These drugs had no significant cytotoxicity as compared with the vehicle control.
    CONCLUSIONS:
    Our data suggested that inhibition of ROS production, possibly through modulation of NOX activity and/or the radical scavenging effect, and beta2 integrin expression in leucocytes indicated that these compounds had the potential to serve as anti-inflammatory agents during oxidative stress.
    In vivo:
    Phytochemistry. 2000 Jan;53(2):253-6.
    Antinociceptive substances from Incarvillea delavayi.[Pubmed: 10680179]
    Antinociceptive activities of an Incarvillea delavayi extract, as well as its constituents, 8-epideoxyloganic acid and delavayine A, were evaluated in the acetic acid induced writhing test in mice.
    METHODS AND RESULTS:
    An oral administration of the delavayi extract weakly decreased the number of writhings and stretchings in this test, in a dose-dependent manner. Furthermore, orally administered 8-epideoxyloganic acid showed weak antinociceptive activity, whereas administration by subcutaneous injection did not. However, subcutaneous injection of delavayine A, a novel monoterpene alkaloid, showed a more significant level of antinociceptive activity.
    Zhongguo Zhong Yao Za Zhi. 2011 Feb;36(4):465-7.
    Constituents and bioactivities of Lamiophlomis rotata.[Pubmed: 21598543]
    To investigate the chemical constituents from Lamiophlomis rotata and the bioactivities of 8-Epideoxyloganic acid.
    METHODS AND RESULTS:
    The constituents were isolated by using a combination of various chromatographic techniques including column chromatography over ployamide, silica gel and Sephadex LH-20. Structures of the isolates were identified by spectroscopic data analysis. Bioactivities were screened by using models in vivo. Five constituents were isolated. 8-Epideoxyloganic acid was isolated for the first time in L. rotata and also in lamioplomis genus. 8-Epideoxyloganic acid could significantly inhibit aectic acid-induced twisting times and slower the time of homeostatsis, also inhibit xylene-induced ear edema in mice.
    CONCLUSIONS:
    8-Epideoxyloganic acid possesses bioactivities of analgesia, homeostasis and anti-inflammatory.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.7747 mL 13.8735 mL 27.7469 mL 55.4939 mL 69.3674 mL
    5 mM 0.5549 mL 2.7747 mL 5.5494 mL 11.0988 mL 13.8735 mL
    10 mM 0.2775 mL 1.3873 mL 2.7747 mL 5.5494 mL 6.9367 mL
    50 mM 0.0555 mL 0.2775 mL 0.5549 mL 1.1099 mL 1.3873 mL
    100 mM 0.0277 mL 0.1387 mL 0.2775 mL 0.5549 mL 0.6937 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
    山栀苷; Shanzhiside CFN98370 29836-27-9 C16H24O11 = 392.4 20mg QQ客服:2159513211
    Negundoside; Negundoside CFN70455 82451-20-5 C23H28O12 = 496.5 5mg QQ客服:1413575084
    水晶兰苷; Monotropein CFN99523 5945-50-6 C16H22O11 = 390.34 20mg QQ客服:1457312923
    Adoxosidic acid; Adoxosidic acid CFN89313 84375-46-2 C16H24O10 = 376.35 5mg QQ客服:1457312923
    Suspenoidside B; Suspenoidside B CFN95071 2161432-08-0 C25H30O12 = 522.5 5mg QQ客服:2056216494
    京尼平苷酸; Geniposidic acid CFN98337 27741-01-1 C16H22O10 = 374.3 20mg QQ客服:1457312923
    鸡屎藤次苷; Scandoside CFN92535 18842-99-4 C16H22O11 = 390.3 5mg QQ客服:1413575084
    去乙酰基车叶草苷酸; Deacetylasperulosidic acid CFN92358 14259-55-3 C16H22O11 = 390.3 20mg QQ客服:1413575084
    车叶草苷酸; Asperulosidic acid CFN92108 25368-11-0 C18H24O12 = 432.4 20mg QQ客服:3257982914
    鸡屎藤苷酸; Paederosidic acid CFN92524 18842-98-3 C18H24O12S = 464.4 20mg QQ客服:1413575084

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