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  • Altholactone

    Altholactone

    Altholactone
    产品编号 CFN97914
    CAS编号 65408-91-5
    分子式 = 分子量 C13H12O4 = 232.2
    产品纯度 >=98%
    物理属性 Oil
    化合物类型 Phenols
    植物来源 The herbs of Goniothalamus malayanus
    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
    Altholactone CFN97914 65408-91-5 1mg QQ客服:1457312923
    Altholactone CFN97914 65408-91-5 5mg QQ客服:1457312923
    Altholactone CFN97914 65408-91-5 10mg QQ客服:1457312923
    Altholactone CFN97914 65408-91-5 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
  • Vin?a Institute of Nuclear Sciences (Serbia)
  • Regional Crop Research Institute (Korea)
  • Universidade Federal de Pernambuco (UFPE) (Brazil)
  • Wageningen University (Netherlands)
  • Semmelweis Unicersity (Hungary)
  • Leibniz Institute of Plant Biochemistry (Germany)
  • University of Lodz (Poland)
  • Indian Institute of Science (India)
  • Institute of Bioorganic Chemistry Polish Academy of Sciences (Poland)
  • University of Vigo (Spain)
  • Instituto Politécnico de Bragan?a (Portugal)
  • Universidade Federal de Santa Catarina (Brazil)
  • University of Mysore (India)
  • Lund University (Sweden)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Eur Rev Med Pharmacol Sci.2020, 24(9):5127-5139.
  • JAOCS2021, 98(7):779-794.
  • Front Pharmacol.2021, 12:615157.
  • Journal of Phytopathology2021, 169,Issue11-12.
  • Molecules.2021, 26(8):2161.
  • Appl Biochem Biotechnol.2022, s12010-022-04166-2.
  • J Pharm Biomed Anal.2019, 164:119-127
  • Life Sci.2023, 317:121458.
  • Journal of Third Military Medical University2019, 41(2):110-115
  • Chinese Pharmacological Bulletin2019, 35(8):1120-1125
  • J Basic Clin Physiol Pharmacol.2016, 27(1):1-8
  • Pharm Biol.2022, 60(1):2040-2048.
  • Plants (Basel).2021, 10(6):1119.
  • United States Patent Application2020, 20200038363
  • J Ethnopharmacol.2019, 235:406-414
  • J Microbiol Biotechnol.2022, 32(2):141-148.
  • Molecules.2018, 23(9):E2121
  • Horticulturae2020, 6(4),76.
  • JPC-Journal of Planar Chromatography2023, 36:179-190
  • Food Chem.2019, 275:746-753
  • Iranian J. Pharm. Res.2021, 20(4):59-70
  • Appl. Sci.2020, 10(8),2804
  • Acta Biochim Pol.2015, 62(2):253-8
  • ...
  • 生物活性
    Description: Altholactone may be a potential antimicrobial agent, particularly in ciprofloxacin-refractory S. aureus and E. faecalis infections. It can inhibit the growth of various types of cancer cells through inducing apoptosis via oxidative stress, including bladder cancer, colon carcinoma cells.
    Targets: ROS | Akt | p38MAPK | Bcl-2/Bax | Caspase | p53 | Antifection
    In vitro:
    Phytother Res. 2012 Jun;26(6):926-31.
    Altholactone induces apoptotic cell death in human colorectal cancer cells.[Pubmed: 22105918]
    Resistance of colorectal cancer (CRC) to the available chemotherapy reveals the demand for identification of new anticancer agents. We evaluated the antitumour potential of Altholactone, a naturally occurring bioactive compound isolated from Goniothalamus spp. (Annonaceae) hooks, against CRC cells.
    METHODS AND RESULTS:
    Antitumour activity of Altholactone was measured using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and the propidium iodide method. Apoptosis mediators involved were assessed using biochemical inhibitors and Western blotting analysis. Results revealed that Altholactone induced varying degrees of apoptosis in CRC cells but not in normal fibroblasts. Dissection of the Altholactone-induced apoptotic signalling pathway revealed that Altholactone activated caspase-dependent and -independent apoptotic pathways. Activation of caspase-4 appeared to be the initiating event in the caspase-dependent apoptotic pathway. Pre-treatment of CRC cells with the antioxidant N-acetylcysteine (NAC) significantly inhibited activation of caspase-4 and Altholactone-induced apoptosis.
    CONCLUSIONS:
    These results indicate that Altholactone induces selective cytotoxicity against colon carcinoma cells and warrants further clinical evaluation.
    Molecules. 2011 Jun 3;16(6):4560-6.
    Altholactone displays promising antimicrobial activity.[Pubmed: 21642933]

    METHODS AND RESULTS:
    The antimicrobial activity of Altholactone, a naturally extracted styryllactone isolated from Goniothalamus malayanus, was determined against Gram positive (S. aureus ATTC 25923, S. aureus ATTC 25392, and E. faecalis ATTC 29212) and Gram negative (E. coli ATTC 35218, S. typhi ATTC 14023 and P. aeruginosa ATCC 27853) reference bacteria and against the fungus C. albicans ATTC 10231. Different concentrations of Altholactone (0, 12, 25, and 50 μg/mL) were used. Results revealed that Altholactone inhibited the growth of all tested microbes except P. aeruginosa ATCC 27853 in a dose-dependent manner, with the highest cytotoxic effects occurring at 50 μg/mL. The average of the inhibition zones of the different concentrations was between 0-30 mm. Furthermore, Altholactone-induced antimicrobial activity against the more sensitive microbes was assessed by measuring the minimal inhibitory concentration (MIC). Results indicated that Gram positive (S. aureus ATTC 25923, S. aureus ATTC 25392, and E. faecalis ATTC 29212) cells were more sensitive to Altholactone than Gram negative ones (E. coli ATTC 35218, S. typhi ATTC 14023). C. albicans showed moderate sensitivity.
    CONCLUSIONS:
    These results indicate that Altholactone might be a potential antimicrobial agent, particularly in ciprofloxacin-refractory S. aureus and E. faecalis infections. Further investigations are required to illustrate the mechanism(s) by which Altholactone produces its antimicrobial effects.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 4.3066 mL 21.5332 mL 43.0663 mL 86.1326 mL 107.6658 mL
    5 mM 0.8613 mL 4.3066 mL 8.6133 mL 17.2265 mL 21.5332 mL
    10 mM 0.4307 mL 2.1533 mL 4.3066 mL 8.6133 mL 10.7666 mL
    50 mM 0.0861 mL 0.4307 mL 0.8613 mL 1.7227 mL 2.1533 mL
    100 mM 0.0431 mL 0.2153 mL 0.4307 mL 0.8613 mL 1.0767 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
    哥纳香三醇; Goniotriol CFN97867 96405-62-8 C13H14O5 = 250.3 5mg QQ客服:215959384
    哥纳香二醇; Goniodiol CFN96049 96422-52-5 C13H14O4 = 234.3 5mg QQ客服:2056216494
    7-乙酸哥纳香二醇酯; Goniodiol 7-acetate CFN97921 96422-53-6 C15H16O5 = 276.3 5mg QQ客服:2056216494
    8-乙酸哥纳香二醇酯; Goniodiol 8-acetate CFN97915 144429-71-0 C15H16O5 = 276.3 5mg QQ客服:1413575084
    二乙酸哥纳香二醇酯; Goniodiol diacetate CFN96047 136778-40-0 C17H18O6 = 318.3 5mg QQ客服:2159513211
    Altholactone; Altholactone CFN97914 65408-91-5 C13H12O4 = 232.2 5mg QQ客服:215959384
    Isoaltholactone; Isoaltholactone CFN97957 124868-11-7 C13H12O4 = 232.2 5mg QQ客服:2159513211

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