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  • 根薯酮内酯AJ

    Taccalonolide AJ

    根薯酮内酯AJ
    产品编号 CFN90935
    CAS编号 1349904-82-0
    分子式 = 分子量 C34H44O14 = 676.7
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Steroids
    植物来源 The rhizomes of Schizocapsa plantaginea Hance
    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
    根薯酮内酯AJ CFN90935 1349904-82-0 1mg QQ客服:1413575084
    根薯酮内酯AJ CFN90935 1349904-82-0 5mg QQ客服:1413575084
    根薯酮内酯AJ CFN90935 1349904-82-0 10mg QQ客服:1413575084
    根薯酮内酯AJ CFN90935 1349904-82-0 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
    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
  • CSIRO - Agriculture Flagship (Australia)
  • Worcester Polytechnic Institute (USA)
  • National Research Council of Canada (Canada)
  • Chinese University of Hong Kong (China)
  • University of Hertfordshire (United Kingdom)
  • University of Liège (Belgium)
  • Universidade da Beira Interior (Germany)
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  • Shanghai University of TCM (China)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Fitoterapia.2021, 153:104995.
  • J Adv Res.2021, 35:245-257.
  • Applied Biological Chemistry2021, 64(4)
  • Plant Physiol Biochem.2019, 144:355-364
  • Nutrients.2019, 11(6):E1380
  • Plants (Basel).2020, 9(11):1422.
  • Nutrients2020, 12(3):811.
  • Food Chem.2019, 274:345-350
  • Viruses.2017, 9(10)
  • J Sci Food Agric.2023, 103(1):213-220.
  • Biochem Biophys Res Commun.2018, 505(4):1148-1153
  • Molecules.2023, 28(7):3039.
  • FASEB J.2019, 33(2):2026-2036
  • Nat Chem Biol.2018, 14(8):760-763
  • Antioxidants (Basel).2020, 9(6):466.
  • Planta Med.2023, a-2192-2281.
  • Virulence.2018, 9(1):588-603
  • Drug Des Devel Ther.2020, 14:969-976.
  • Korean J of Medicinal Crop Science2018, 220-226
  • J Ethnopharmacol.2017, 198:87-90
  • Nutrients2020, 12(2):488
  • Food Science and Biotechnology2023, 2023:1007
  • Molecules2022, 27(14),4462
  • ...
  • 生物活性
    Description: Taccalonolide AJ is a microtubule stabilizer; it has excellent and highly persistent antitumor efficacy when administered directly to the tumor, suggesting that the lack of antitumor efficacy seen with systemic administration of AJ is likely due to its short half-life in vivo.
    In vivo:
    J Nat Prod. 2017 Feb 24;80(2):409-414.
    Pharmacokinetic Analysis and in Vivo Antitumor Efficacy of Taccalonolides AF and AJ.[Pubmed: 28112516 ]
    The taccalonolides are microtubule stabilizers that covalently bind tubulin and circumvent clinically relevant forms of resistance to other drugs of this class. Efforts are under way to identify a taccalonolide with optimal properties for clinical development. The structurally similar taccalonolides AF and AJ have comparable microtubule-stabilizing activities in vitro, but taccalonolide AF has excellent in vivo antitumor efficacy when administered systemically, while taccalonolide AJ does not elicit this activity even at maximum tolerated dose.
    METHODS AND RESULTS:
    The hypothesis that pharmacokinetic differences underlie the differential efficacies of taccalonolides AF and AJ was tested. The effects of serum on their in vivo potency, metabolism by human liver microsomes and in vivo pharmacokinetic properties were evaluated. Taccalonolides AF and AJ were found to have elimination half-lives of 44 and 8.1 min, respectively. Furthermore, taccalonolide AJ was found to have excellent and highly persistent antitumor efficacy when administered directly to the tumor, suggesting that the lack of antitumor efficacy seen with systemic administration of AJ is likely due to its short half-life in vivo.
    CONCLUSIONS:
    These results help define why some, but not all, taccalonolides inhibit the growth of tumors at systemically tolerable doses and prompt studies to further improve their pharmacokinetic profile and antitumor efficacy.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.4778 mL 7.3888 mL 14.7776 mL 29.5552 mL 36.944 mL
    5 mM 0.2956 mL 1.4778 mL 2.9555 mL 5.911 mL 7.3888 mL
    10 mM 0.1478 mL 0.7389 mL 1.4778 mL 2.9555 mL 3.6944 mL
    50 mM 0.0296 mL 0.1478 mL 0.2956 mL 0.5911 mL 0.7389 mL
    100 mM 0.0148 mL 0.0739 mL 0.1478 mL 0.2956 mL 0.3694 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
    酸浆苦味素G; Physalin G CFN95104 76045-38-0 C28H30O10 = 526.5 5mg QQ客服:1457312923
    异酸浆苦味素G; Isophysalin G CFN95328 152221-21-1 C28H30O10 = 526.5 5mg QQ客服:215959384
    酸浆苦味H; Physalin H CFN92937 70241-09-7 C28H31ClO10 = 562.99 5mg QQ客服:215959384
    4,7-二脱氢新酸浆苦素B; 4,7-Didehydroneophysalin B CFN95317 134461-76-0 C28H28O9 = 508.5 5mg QQ客服:2056216494
    酸浆苦味素X; Physalin X CFN95329 72497-31-5 C28H30O10 = 526.5 5mg QQ客服:2056216494
    根薯酮内酯A; Taccalonolide A CFN90596 108885-68-3 C36H46O14 = 702.74 10mg QQ客服:3257982914
    根薯酮内酯AJ; Taccalonolide AJ CFN90935 1349904-82-0 C34H44O14 = 676.7 5mg QQ客服:1457312923
    酸浆苦素L; Physalin L CFN90166 113146-74-0 C28H32O10 = 528.55 5mg QQ客服:2056216494
    酸浆苦味A; Physalin A CFN92940 23027-91-0 C28H30O10 = 526.5 5 mg QQ客服:1413575084
    酸浆苦素O; Physalin O CFN95097 120849-18-5 C28H32O10 = 528.55 5mg QQ客服:2056216494

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