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  • 天冬宁B

    Shatavarin IV

    天冬宁B
    产品编号 CFN70458
    CAS编号 84633-34-1
    分子式 = 分子量 C45H74O17 = 887.1
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Steroids
    植物来源 The roots of Asparagus racemosus
    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
    天冬宁B CFN70458 84633-34-1 1mg QQ客服:1413575084
    天冬宁B CFN70458 84633-34-1 5mg QQ客服:1413575084
    天冬宁B CFN70458 84633-34-1 10mg QQ客服:1413575084
    天冬宁B CFN70458 84633-34-1 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
  • University of Limpopo (South Africa)
  • Warszawski Uniwersytet Medyczny (Poland)
  • Aarhus University (Denmark)
  • Macau University of Science and Technology (China)
  • University of East Anglia (United Kingdom)
  • Rio de Janeiro State University (Brazil)
  • Lund University (Sweden)
  • Korea Intitute of Science and Technology (KIST) (Korea)
  • Helmholtz Zentrum München (Germany)
  • University of the Basque Country (Spain)
  • Auburn University (USA)
  • National Chung Hsing University (Taiwan)
  • Tokyo Woman's Christian University (Japan)
  • Heinrich-Heine-University Düsseldorf (Germany)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • PLoS One.2017, 12(8):e0181191
  • World J Mens Health.2019, 10.5534
  • BMC Complement Med Ther.2023, 23(1):264.
  • Mol Microbiol.2019, 112(1):317-332
  • Am J Chin Med.2016, 44(8):1719-1735
  • Front Cell Dev Biol.2021, 9:764263.
  • Molecules.2019, 24(9):E1719
  • Plant Physiol Biochem.2023, 201:107795.
  • Molecules.2023, 28(16):6025.
  • J. Pharm. Res. Int.2022, 34(58): pp.1-14.
  • LWT2021, 147:111620.
  • Int J Anal Chem.2017, 2017:1254721
  • Front Plant Sci.2018, 9:1424
  • Evid Based Complement Alternat Med.2022, 2022:1307173.
  • Sains Malaysiana2022, 51(4):1143-1154
  • Biofactors.2018, 44(2):168-179
  • J Ethnopharmacol.2016, 192:370-381
  • Journal of functional foods2018, 171-182
  • Food Funct.2022, 13(14):7638-7649.
  • Evid Based Complement Alternat Med.2021, 2021:8850744.
  • Int J Biol Macromol.2019, 126:653-661
  • J Applied Biological Chemistry2021, 64(2):185-192
  • Phytomedicine.2019, 57:95-104
  • ...
  • 生物活性
    Description: Shatavarin IV shows in vitro anti-malassezia activity. Shatavarins (containing shatavarin IV) rich fraction (AR-2B) exhibits significant anticancer activity in both in vitro and in vivo experimental models.
    In vitro:
    International journal of cosmetic ence, 2013, 36(1):74-78.
    In vitro Anti-Malassezia Activity and Potential Use in Anti-dandruff Formulation of Asparagus racemosus.[Reference: WebLink]
    Malassezia species are frequently associated with dandruff and seborrhoeic dermatitis. The study was conducted to evaluate anti-fungal activities of the extracts obtained from the roots of Asparagus racemosus Willd against Malassezia furfur and M. globosa.
    METHODS AND RESULTS:
    Asparagus racemosus roots were successively extracted with the series of solvents, that is, hexane, ethanol and water, and also a saponin-enriched fraction was prepared. The amounts of saponin (equivalent to shatavarin IV) in the extracts were determined using ELISA. The extracts were tested for anti-fungal activity by disc diffusion and broth microdilution methods. By disc diffusion, only the ethanolic and saponin-enriched extracts demonstrated anti-fungal activity against M. furfur and M. globosa at the concentration of 1 mg per disc whereas the extracts with other solvents were ineffective. Multiple concentrations using the broth microdilution method against M. furfur and M. globosa yielded minimum inhibitory concentrations (MICs) of 25 mg mL(-1) for the ethanolic extract but much higher potency for the saponin-enriched extract: MICs to 0.20 and 0.40 mg mL(-1) for M. furfur and M. globosa, respectively. These extracts showed no antagonist effect with the anti-fungal agents, ketoconazole and zinc pyrithione.
    CONCLUSIONS:
    These studies revealed the antifungal activity of A. racemosus roots extracts. Because A. racemosus is also anti-inflammatory agent, it has the potential use as an active ingredient in an anti-dandruff formulation.
    In vivo:
    Indian Journal of Pharmacology, 2012, 44(6):732.
    Shatavarins (containing Shatavarin IV) with anticancer activity from the roots of Asparagus racemosus.[Reference: WebLink]
    The anticancer activity of shatavarins (containing shatavarin IV) isolated from the roots of Asparagus racemosus (Wild) was evaluated using in vitro and in vivo experimental models.
    METHODS AND RESULTS:
    The shatavarin IV was isolated from ethyl acetate insoluble fraction (AR-2B) of chloroform:methanol (2:1) (AR-2) extract of A. racemosus roots. The cytotoxicity (in vitro) of shatavarin IV and other shatavarins rich fraction was carried out using of MTT assay using MCF-7 (human breast cancer), HT-29 (human colon adenocarcinoma), and A-498 (human kidney carcinoma) cell lines. The in vivo anticancer activity of shatavarins (containing shatavarin IV) was evaluated against Ehrlich ascites carcinoma (EAC) tumor bearing mice. The isolated shatavarin IV (84.69 %) along with shatavarins rich fraction, coded AR-2B containing 5.05% shatavarin IV showed potent cytotoxicity. Oral administration of AR-2B to tumor bearing mice at doses of 250 and 500 mg/kg body weight for 10 days, showed significant reduction in percent increase in body weight, tumor volume, packed cell volume, viable tumor cell count, and increased non-viable cell count when compared to the untreated mice of the EAC control group. The restoration of hematological parameters towards normalcy was also observed.
    CONCLUSIONS:
    The result suggests that the shatavarins (containing shatavarin IV) rich fraction (AR-2B) exhibits significant anticancer activity in both in vitro and in vivo experimental models.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.1273 mL 5.6363 mL 11.2727 mL 22.5454 mL 28.1817 mL
    5 mM 0.2255 mL 1.1273 mL 2.2545 mL 4.5091 mL 5.6363 mL
    10 mM 0.1127 mL 0.5636 mL 1.1273 mL 2.2545 mL 2.8182 mL
    50 mM 0.0225 mL 0.1127 mL 0.2255 mL 0.4509 mL 0.5636 mL
    100 mM 0.0113 mL 0.0564 mL 0.1127 mL 0.2255 mL 0.2818 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
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    萜品油烯; Terpinolene CFN70155 586-62-9 C10H16 = 136.2 20mg QQ客服:2056216494
    留柯诺内酰胺; Leuconolam CFN97509 93710-27-1 C19H22N2O3 = 326.4 5mg QQ客服:215959384

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