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  • 蓟苦素

    Cnicin

    蓟苦素
    产品编号 CFN70320
    CAS编号 24394-09-0
    分子式 = 分子量 C20H26O7 = 378.4
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Sesquiterpenoids
    植物来源 The herbs of Centaurea maculosa
    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
    蓟苦素 CFN70320 24394-09-0 1mg QQ客服:3257982914
    蓟苦素 CFN70320 24394-09-0 5mg QQ客服:3257982914
    蓟苦素 CFN70320 24394-09-0 10mg QQ客服:3257982914
    蓟苦素 CFN70320 24394-09-0 20mg QQ客服:3257982914
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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
  • University of Toulouse (France)
  • University of East Anglia (United Kingdom)
  • Kamphaengphet Rajabhat University (Thailand)
  • Florida A&M University (USA)
  • University of Eastern Finland (Finland)
  • Nicolaus Copernicus Uniwersity (Poland)
  • University of Auckland (New Zealand)
  • University of Padjajaran (Indonesia)
  • Deutsches Krebsforschungszentrum (Germany)
  • University of Bordeaux (France)
  • Johannes Gutenberg University Mainz (JGU) (Germany)
  • Yale University (USA)
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  • Universidade do Porto (Portugal)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Biosci Rep.2018, 38(4)
  • Int J Mol Sci.2018, 19(9):E2601
  • Phytomedicine2022, 104:154318
  • Journal of Third Military Medical University2018, 40(12):1073-1078
  • Tropical J. of Pha. Research2017, 16(3):543-552
  • Cells.2022, 11(8), 1311.
  • Nutrients.2017, 10(1)
  • Food Sci Nutr.2023, 00:1-10.
  • J Med Food.2016, 19(12):1155-1165
  • Front Pharmacol.2021, 12:615157.
  • Biomol Ther (Seoul).2023, 31(1):40-47.
  • Oncol Rep.2021, 46(2):166.
  • Mediators Inflamm.2016, 2016:7216912
  • J Breast Cancer.2015, 18(2):112-118
  • Food Res Int.2021, 148:110607.
  • PLoS One.2018, 13(4):e0195642
  • Int J Mol Sci.2021, 22(2):770.
  • Journal of Functional Foods2022, 98:105271.
  • JEJU National University2022, 24032.
  • Nature Ecology & Evolution2020, doi: 10.1038
  • Sci Rep.2018, 8:15059
  • Evid Based Complement Alternat Med.2016, 2016:4357656
  • Int J Mol Sci.2020, 21(24):9369.
  • ...
  • 生物活性
    Description: Cnicin has anti-inflammatory, antibiotic, antibacterial and cytotoxic activities. It blocks the water uptake by roots inhibiting subsequent seedling growth but has no effect during germination.
    Targets: NF-κB | NOS | Antifection
    In vitro:
    Journal of Chemical Ecology, 01 Apr 1994, 20(4):929-942.
    Influence of cnicin, a sesquiterpene lactone ofCentaurea maculosa (Asteraceae), on specialist and generalist insect herbivores.[Reference: WebLink]
    The sesquiterpene lactone cnicin was extracted fromCentaurea maculosa andCentaurea vallesiaca. We examined its effects on the ovipositional response and larval development of generalist and specialist insect herbivores associated withC. maculosa.
    METHODS AND RESULTS:
    For the oviposition trials, three plant species (C. maculosa, Achillea millefolium, andCichorium intybus), half of which were sprayed with 3% of cnicin, were exposed to the specialist mothsStenodes straminea, Agapeta zoegana, andPterolonche inspersa in field cages. All three species significantly preferredC. maculosa to other plants andP. inspersa significantly preferred cnicin-sprayed plants to untreated plants for oviposition. Tested over all species, cnicin significantly increased the number of eggs laid on a given plant. A larval diet test examined the toxicity of cnicin for larvae of the generalist noctuid mothSpodoptera littoralis. Cnicin concentrations of 3% and 6% were lethal and 1% and 0.5% seriously inhibited growth and development. The larvae of theC. maculosa specialistStenodes straminea survived at 6% cnicin, but none of the pupae hatched.Agapeta zoegana was able to survive at 1% and 3% cnicin. Both specialists had difficulties with the artificial diet, but weight increase and survival was not further reduced when cnicin was present compared with on the control diet.
    CONCLUSIONS:
    In conclusion, cnicin influenced host recognition by the specialist species, and larvae of the generalist did not survive on natural levels of cnicin. Growth and survival of the specialist were not influenced by cnicin but were considerably hampered on artificial diet.
    Pharmaceutical Biology, 2010,49(8):840-849.
    Secondary metabolites of Centaurea calolepis and evaluation of cnicin for anti-inflammatory, antioxidant, and cytotoxic activities.[Reference: WebLink]
    Secondary metabolite determination, isolation and structure elucidation of pure compounds were performed on C. calolepis. Cnicin, which is the main component of several Centaurea species, was tested for its in vitro anti-inflammatory, antioxidant and cytotoxic activities.
    METHODS AND RESULTS:
    Chloroform and methanol extracts of the aerial parts of C. calolepis were subjected to isolation process using column chromatography. The structures of the compounds were characterized by 1D- and 2D-NMR experiments. Thin–layer chromatography and high performance liquid chromatography were used in determination of phenolics. Cnicin was subjected to a panel of cellular assays to test for inhibition of nuclear factor κB (NF-κB), inducible nitric oxide synthase (iNOS), reactive oxygen species and cytotoxicity. Cnicin, lucenin-2, schaftoside and 3-O-feruloylquinic acid were isolated from C. calolepis extracts. Vicenin-2, vitexin, isovitexin, homoorientin, rutin, orientin, luteolin-7-O-glycoside and chlorogenic acid were determined in fractions. Cnicin showed inhibition of NF-κB and inhibition of iNOS activity with IC50 Values of 1.8 and 6.5 µM, respectively. Cytotoxic activity of cnicin was observed toward pig kidney epithelial (LLC-PK11), human malignant melanoma (SK-MEL) and human ductal carcinoma (BT-549) cells with IC50 values of 23.3, 14.0 and 18.3 µM, respectively.
    CONCLUSIONS:
    This is the first detailed report of secondary metabolites of C. calolepis. Evaluation of biological activity of cnicin establishes the potential of this compound as an anti-inflammatory and cytotoxic agent.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.6427 mL 13.2135 mL 26.4271 mL 52.8541 mL 66.0677 mL
    5 mM 0.5285 mL 2.6427 mL 5.2854 mL 10.5708 mL 13.2135 mL
    10 mM 0.2643 mL 1.3214 mL 2.6427 mL 5.2854 mL 6.6068 mL
    50 mM 0.0529 mL 0.2643 mL 0.5285 mL 1.0571 mL 1.3214 mL
    100 mM 0.0264 mL 0.1321 mL 0.2643 mL 0.5285 mL 0.6607 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
    表大戟二烯醇; Tirucallol CFN89512 514-46-5 C30H50O = 426.71 5mg QQ客服:1413575084
    新补骨脂异黄酮; Neobavaisoflavone CFN92222 41060-15-5 C20H18O4 = 322.4 20mg QQ客服:1457312923
    柚皮素; 4',5,7-三羟基黄烷酮; Naringenin CFN98742 480-41-1 C15H12O5 = 272.3 20mg QQ客服:2159513211
    二乙酸丁香三环烷二醇酯; Clovanediol diacetate CFN98309 2649-68-5 C19H30O4 = 322.4 5mg QQ客服:2056216494

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