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  • 棉花素

    Gossypetin

    棉花素
    产品编号 CFN91897
    CAS编号 489-35-0
    分子式 = 分子量 C15H10O8 = 318.24
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Flavonoids
    植物来源 The herbs of Rhodiola rosea
    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
    棉花素 CFN91897 489-35-0 1mg QQ客服:2056216494
    棉花素 CFN91897 489-35-0 5mg QQ客服:2056216494
    棉花素 CFN91897 489-35-0 10mg QQ客服:2056216494
    棉花素 CFN91897 489-35-0 20mg QQ客服:2056216494
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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
  • The Institute of Cancer Research (United Kingdom)
  • Almansora University (Egypt)
  • Institute of Pathophysiology Medical University of Vienna (Austria)
  • VIT University (India)
  • Monash University Malaysia (Malaysia)
  • University of Melbourne (Australia)
  • Universidad de Buenos Aires (Argentina)
  • University of Bordeaux (France)
  • Korea Institute of Oriental Medicine (Korea)
  • Sapienza University of Rome (Italy)
  • Sri Sai Aditya Institute of Pharmaceutical Sciences and Research (India)
  • University of Otago (New Zealand)
  • Ain Shams University (Egypt)
  • University of British Columbia (Canada)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Pharmacognosy Journal, 2021, 13(5).
  • Evid Based Complement Alternat Med.2018, 2018:4259603
  • Plants (Basel).2020, 9(11):1555.
  • Int J Nanomedicine.2022, 17:6513-6525.
  • Evid Based Complement Alternat Med.2016, 2016:1739760
  • Vietnam Journal of Food Control.2022, 5(2): 115-128.
  • Molecules.2022, 27(22):7887.
  • Molecules.2019, 24(17):E3127
  • Front Chem.2023, 11:1245071.
  • BMC Plant Biol.2021, 21(1):60.
  • Food Chem.2019, 276:768-775
  • Appl. Sci.2020, 10(4),1304
  • Ann Transl Med.2019, 7(23):731
  • Food Chem.2020, 327:126992.
  • Appl. Sci.2020, 10(20),7374.
  • J Korean Med Obes Res.2023, 23:10-7
  • J Appl Microbiol.2022, 132(2):949-963.
  • J Biosci.2020, 45:46.
  • J Enzyme Inhib Med Chem.2019, 34(1):134-143
  • J. of The Korean Society of Food Culture2017, 144-149
  • Free Radic Biol Med.2016, 97:307-319
  • Research Square2021, March 3rd.
  • Molecules.2021, 26(9):2802.
  • ...
  • 生物活性
    Description: Gossypetin has anti-mutagenic, anti-atherosclerotic, antioxidant, as well as cytoprotective and antimicrobial effects, it inhibits bone resorption through down-regulating lysosomal cathepsin K activity and autophagy-related protein induction in actin ring-bearing osteoclasts. Gossypetin ameliorates ionizing radiation-induced oxidative stress in mice liver, it shows radioprotective action against gamma (γ)-radiation-induced oxidative stress. Gossypetin is an inducer of apoptotic and autophagic cell death in LNCaP cells, and provide a new mechanism for its anticancer activity.
    Targets: PI3K | ATPase | MMP(e.g.TIMP) | NF-kB | Nrf2 | JNK
    In vitro:
    Journal of Functional Foods, 2016, 24:390-402.
    Dietary compound gossypetin inhibits bone resorption through down-regulating lysosomal cathepsin K activity and autophagy-related protein induction in actin ring-bearing osteoclasts[Reference: WebLink]
    Gossypetin, usually isolated from the flowers and the calyx of Hibiscus sabdariffa, possesses anti-microbial and anti-atherosclerotic effects. However, anti-osteoporotic effects of Gossypetin have not been elucidated.
    METHODS AND RESULTS:
    Gossypetin attenuated RANKL-induced multinucleated osteoclast formation with enhanced TRAP activity and blunted bone resorption active in osteoclasts. Gossypetin inhibited the actin ring formation and αvβ3 integrin induction for sealing zones. This compound suppressed the induction of CAII, V-ATPase, ClC-7 and Ae2, all required for secretion of proton and chloride ions into resorption lacunae. Furthermore, Gossypetin reduced lysosomal cathepsin K transcription and MMP-9 activity, blunting accumulation of lysosomes in osteoclasts displaying an actin ring. The presence of Gossypetin deterred the induction of Rab7, and Atg12–Atg5 conjugate and Atg7 involved in LC3 lipidation, all prerequisites to osteoclast ruffled border formation.
    CONCLUSIONS:
    These observations demonstrate for the first time that Gossypetin was effective in retarding ruffled border formation and acidification in a sealed microenvironment of osteoclast resorption lacunae.
    Medicinal Chemistry,2016, 6(2).
    Protective Role of Gossypetin against Cyclophosphamide Toxicity in Human Lymphocyte Culture In vitro[Reference: WebLink]
    Gossypetin is a flavonoid which has anti-mutagenic, anti-atherosclerotic, antioxidant, as well as cytoprotective and antimicrobial effects. The objective of this study was to investigate the cytoprotective role of Gossypetin (GP) against cyclophosphamide (CP) toxicity in the human lymphocyte culture.
    METHODS AND RESULTS:
    Cytotoxic, necrotic and apoptotic effects of CP (1mM), GP (25, 50 and 100 μM) and combination of them (CP+GP) were studied by using MTT assay and Flow cytometry analysis. It was detected that CP significantly decreased cell viability rate via arresting cell cycle and increasing apoptosis/necroptosis. However, GP treatment reduced negative effects of CP at different concentrations. The most effective concentration of GP against CP toxicity was 25 μM. This concentration GP increased live cell number and cell viability, in addition decreased necrotic and late apoptotic cell quantity which were treated with CP.
    CONCLUSIONS:
    These results suggest that GP could attenuate the cytotoxic effects of CP and protect the healthy cells when it is used during chemotherapy.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.1423 mL 15.7114 mL 31.4228 mL 62.8457 mL 78.5571 mL
    5 mM 0.6285 mL 3.1423 mL 6.2846 mL 12.5691 mL 15.7114 mL
    10 mM 0.3142 mL 1.5711 mL 3.1423 mL 6.2846 mL 7.8557 mL
    50 mM 0.0628 mL 0.3142 mL 0.6285 mL 1.2569 mL 1.5711 mL
    100 mM 0.0314 mL 0.1571 mL 0.3142 mL 0.6285 mL 0.7856 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
    槲皮素3,4'-二甲醚; 5,7,3'-三羟基-3,4'-二甲氧基黄酮; Quercetin 3,4'-dimethyl ether CFN98429 33429-83-3 C17H14O7 = 330.3 5mg QQ客服:2159513211
    商陆素; 3,5 ,3'-三羟基-7,4'-二甲氧基黄酮; Ombuin CFN98876 529-40-8 C17H14O7 = 330.3 5mg QQ客服:2056216494
    阿亚黄素,缎木素; Ayanin CFN96157 572-32-7 C18H16O7 = 344.3 10mg QQ客服:215959384
    矢车菊黄素; Centaureidin CFN90433 17313-52-9 C18H16O8 = 360.31 5mg QQ客服:2159513211
    甲氧基万寿菊素; Axillarin CFN89530 5188-73-8 C17H14O8 = 346.28 5mg QQ客服:2159513211
    蔓荆子黄素; Vitexicarpin CFN98172 479-91-4 C19H18O8 = 374.34 20mg QQ客服:3257982914
    异鼠李素; Isorhamnetin CFN98735 480-19-3 C16H12O7 = 316.3 20mg QQ客服:3257982914
    槲皮素-3,3'-二甲醚; Quercetin 3,3'-dimethyl ether CFN89506 4382-17-6 C17H14O7 = 330.28 5mg QQ客服:1413575084
    槲皮素3,5,3'-三甲基醚; Quercetin 3,5,3'-trimethyl ether CFN91556 13459-09-1 C18H16O7 = 344.3 5mg QQ客服:215959384
    甲基鼠李素; Rhamnazin CFN70409 552-54-5 C17H14O7 = 330.3 5mg QQ客服:3257982914

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