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  • 19 alpha-Hydroxyasiatic acid

    19 alpha-Hydroxyasiatic acid

    19 alpha-Hydroxyasiatic acid
    产品编号 CFN91072
    CAS编号 70868-78-9
    分子式 = 分子量 C30H48O6 = 504.7
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Triterpenoids
    植物来源 The herbs of Sanguisorba officinalis
    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
    19 alpha-Hydroxyasiatic acid CFN91072 70868-78-9 1mg QQ客服:1413575084
    19 alpha-Hydroxyasiatic acid CFN91072 70868-78-9 5mg QQ客服:1413575084
    19 alpha-Hydroxyasiatic acid CFN91072 70868-78-9 10mg QQ客服:1413575084
    19 alpha-Hydroxyasiatic acid CFN91072 70868-78-9 20mg 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
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  • University of Hertfordshire (United Kingdom)
  • Biotech R&D Institute (USA)
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  • Fraunhofer-Institut für Molekularbiologie und Angewandte ?kologie IME (Germany)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Appl. Sci. 2021, 11(23),11099.
  • Metab Eng.2022, 75:143-152.
  • Legume Science2021, 3(4): e101.
  • Kangwon National University2022, 37(1):29-37
  • In Vitro Cellular & Developmental Biology - Plant2022, 58:972-988.
  • Molecules.2020, 25(9):2081.
  • Int J Mol Sci.2020, 21(6):2190.
  • Foods.2022, 12(1):136.
  • J Drug Delivery Science and Tech.2022, 67:102957.
  • Oxid Med Cell Longev.2020, 2020:8887251.
  • J.Food Processing & Preservation2022, jfpp.16666
  • Mol Med Rep.2022, 25(1):8.
  • Life Sci.2019, 216:259-270
  • Journal of Third Military Medical University2019, 41(2):110-115
  • Plants (Basel).2022, 11(21):2947.
  • LWT - Food Science and Technology2022, 164:113627
  • Molecules 2022, 27(3),960.
  • Regul Toxicol Pharmacol.2023, 142:105433.
  • J Breast Cancer.2015, 18(2):112-118
  • Molecules.2020, 25(21):5087.
  • Phytochemistry.2021, 181:112539.
  • Pharm Biol.2022, 60(1):2040-2048.
  • Evid Based Complement Alternat Med.2022, 2022:1307173.
  • ...
  • 生物活性
    Description: 19 alpha-Hydroxyasiatic acid shows significant anticoagulant effect on the extrinsic pathway.
    In vitro:
    Food Chemistry, 2009, 116(3):633-637.
    Ursolic acid analogues: non-phenolic functional food components in Jamaican raspberry fruits[Reference: WebLink]
    The Rubus genus produces numerous species that are known for their medicinal properties. Rubus rosifolius, called the red raspberry, grows wild in elevated regions in Jamaica.
    METHODS AND RESULTS:
    Phytochemical examination of the ethyl acetate extract of the fruit yielded eight compounds of the 19-α-hydroxyursane type: euscaphic acid (1), 1-β-hydroxyeuscaphic acid (2), hyptatic acid B (3), 19 alpha-Hydroxyasiatic acid(4), trachelosperogenin (5), 4-epi-nigaichigoside F1 (6), nigaichigoside F1 (7), and trachelosperoside B-1 (8), as confirmed by NMR spectroscopy. Inhibition of cell proliferation by these compounds were determined by using MCF-7 (breast), SF-268 (CNS), NCI H460 (lung), HCT-116 (colon) and AGS (gastric) human tumour cells. Among the human tumour cell lines assayed, only compounds 3 and 6 displayed significant growth inhibition and was specific to colon tumour cells by 56% and 40%, respectively. These ursolic acid analogues were also tested for anti-inflammatory activity using in vitro cycloxegenase-1 (COX-1) and cycloxegenase-2 (COX-2) enzyme inhibitory assays.
    CONCLUSIONS:
    Compounds 1, 2 and 3 showed selective COX-1 enzyme inhibitory activity (13%, 25% and 35%) at 25 μg/ml. In the lipid peroxidation (LPO) inhibitory assays, compounds 2, 4, 7 and 6 inhibited LPO by 62%, 60%, 53% and 68%, respectively, at 25 μg/ml.
    Chem Pharm Bull (Tokyo). 2007 May;55(5):784-8.
    Production of triterpene acids by cell suspension cultures of Olea europaea.[Pubmed: 17473469 ]
    Olive (Olea europaea) contains large quantity of triterpene acids including oleanolic acid (6) as a major one. Varieties of biological activities exhibited by triterpene acids attracted our attentions, especially from pharmaceutical viewpoints. Cell culture of olive plant was induced and its triterpene constituents were studied.
    METHODS AND RESULTS:
    From the cell suspension cultures, six ursane type triterpene acids; ursolic acid (9), pomolic acid (10), rotundic acid (11), tormentic acid (12), 2alpha-hydroxyursolic acid (13) and 19 alpha-hydroxyasiatic acid (14), and two oleanane type acids; oleanolic acid and maslinic acid (7), have been isolated. Quantity of ursane type triterpene acids produced by cell cultures was larger than that of oleanane type. Further, a multifunctional oxidosqualene cyclase (OSC) named OEA was cloned by homology based PCRs from the same cultured cells.
    CONCLUSIONS:
    Major product of OEA is alpha-amyrin (ursane skeleton), showing good accordance to higher content of ursane-type triterpene acids in the cultured cells, and strongly suggesting OEA to be a major contributor OSC for their production.
    Phytotherapy Research, 1998, 12(2):146-148.
    The anticoagulant effects ofGeum japonicum extract and its constituents.[Reference: WebLink]

    METHODS AND RESULTS:
    Anticoagulation activity-guided fractionation led to the isolation of seven triterpenoid compounds from the methanol extract of the whole plant of Geum japonicum and their identification was based on spectroscopic methods.
    CONCLUSIONS:
    Of these compounds, 19 alpha-Hydroxyasiatic acid (2α, 3β, 19α, 23-tetrahydroxy-12-ursen-28-oic-acid) showed significant anticoagulant effect on the extrinsic pathway.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.9814 mL 9.9069 mL 19.8138 mL 39.6275 mL 49.5344 mL
    5 mM 0.3963 mL 1.9814 mL 3.9628 mL 7.9255 mL 9.9069 mL
    10 mM 0.1981 mL 0.9907 mL 1.9814 mL 3.9628 mL 4.9534 mL
    50 mM 0.0396 mL 0.1981 mL 0.3963 mL 0.7926 mL 0.9907 mL
    100 mM 0.0198 mL 0.0991 mL 0.1981 mL 0.3963 mL 0.4953 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
    2alpha,3alpha,19alpha,23-四羟基乌苏-12-烯-28-酸 ; Myrianthic acid CFN96828 89786-84-5 C30H48O6 = 504.70 5mg QQ客服:2056216494
    19 alpha-Hydroxyasiatic acid; 19 alpha-Hydroxyasiatic acid CFN91072 70868-78-9 C30H48O6 = 504.7 10mg QQ客服:3257982914
    Myrianthic acid 3,23-acetonide; Myrianthic acid 3,23-acetonide CFN89232 578710-52-8 C33H52O6 = 544.77 5mg QQ客服:3257982914
    去羟加利果酸; Esculentic acid CFN99059 103974-74-9 C30H48O5 = 488.7 5mg QQ客服:2056216494
    (2ALPHA,3BETA,4ALPHA)-2,3,23-三羟基乌苏-12,20(30)-二烯-28-酸; Actinidic acid CFN98444 341971-45-7 C30H46O5 = 486.7 5mg QQ客服:2056216494
    积雪草酸; Asiatic acid CFN98688 464-92-6 C30H48O5 = 488.7 20mg QQ客服:2056216494
    3-O-香豆酰积雪草酸; 3-O-Coumaroylasiatic acid CFN96830 143773-52-8 C39H54O7 = 634.85 5mg QQ客服:215959384
    积雪草苷; Asiaticoside CFN99912 16830-15-2 C48H78O19 = 959.12 20mg QQ客服:2159513211
    羟基积雪草苷; Madecassoside CFN99913 34540-22-2 C48H78O20 = 975.13 20mg QQ客服:1457312923
    积雪草苷B; Asiaticoside B CFN95124 125265-68-1 C48H78O20 = 975.13 20mg QQ客服:3257982914

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