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  • 樱花亭

    Sakuranetin

    樱花亭
    产品编号 CFN98366
    CAS编号 2957-21-3
    分子式 = 分子量 C16H14O5 = 286.3
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Flavonoids
    植物来源 The leaves of Oryza sativa L.
    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
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    产品名称 产品编号 CAS编号 包装 QQ客服
    樱花亭 CFN98366 2957-21-3 10mg QQ客服:1413575084
    樱花亭 CFN98366 2957-21-3 20mg QQ客服:1413575084
    樱花亭 CFN98366 2957-21-3 50mg QQ客服:1413575084
    樱花亭 CFN98366 2957-21-3 100mg 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
  • Universite Libre de Bruxelles (Belgium)
  • Chiang Mai University (Thailand)
  • Tohoku University (Japan)
  • Vin?a Institute of Nuclear Sciences (Serbia)
  • University of Pretoria (South Africa)
  • St. Jude Children Research Hospital (USA)
  • Helmholtz Zentrum München (Germany)
  • Ain Shams University (Egypt)
  • Medizinische Universit?t Wien (Austria)
  • Chungnam National University (Korea)
  • Utah State University (USA)
  • Kazusa DNA Research Institute (Japan)
  • University of Hawaii Cancer Center (USA)
  • University of Parma (Italy)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Evid Based Complement Alternat Med.2018, 2018:4259603
  • Food Chem.2020, 327:126992.
  • Chem Biodivers.2023, 20(10):e202300741.
  • Cardiovasc Toxicol.2021, 21(11):947-963.
  • Applied Biological Chemistry2023, 66:85.
  • VNU Journal of Science2023, No. 20.
  • Bio-protocol2018, 9(14):e3301
  • Journal of Chromatography A2020, 460942
  • Horticulture Research2023, uhad164.
  • Phytochemistry.2017, 141:162-170
  • BMC Complement Altern Med.2018, 18(1):221
  • Food Chem.2019, 276:768-775
  • Antioxidants (Basel).2020, 9(2):E120
  • Antiviral Res.2021, 193:105142.
  • Institute of Food Science & Technology2021, 56(11).
  • Chem Biol Interact.2019, 315:108910
  • J Sci Food Agric.2023, 103(1):213-220.
  • Evid Based Complement Alternat Med.2020, 2020:2584783.
  • J Clin Med.2019, 8(10):E1664
  • Plants (Basel).2021, 10(11):2525.
  • Kaohsiung J Med Sci.2023, 10.1002/kjm2.12764
  • Phytomedicine.2018, 40:37-47
  • Antibiotics.2022, 11(4), 510.
  • ...
  • 生物活性
    Description: Sakuranetin, a flavanone phytoalexin from ultraviolet-irradiated rice leaves, it has antifungal, antimutagenic, anti-inflammatory and antioxidant effects, it shows a suppressive effect on umu gene expression of SOS response in Salmonella typhimurium TA1535/pSK1002 against the mutagen furylfuramide. Sakuranetin may contribute to maintain glucose homeostasis in animals, it can strongly induce differentiation of 3T3-L1 preadipocytes, stimulate glucose uptake in differentiated 3T3-L1 adipocytes.Sakuranetin stimulates melanogenesis in B16 melanoma cells via inhibition of ERK1/2 and PI3K/AKT signaling pathways, which lead to upregulation of Tyr, TRP1, and TRP2.
    Targets: PPAR | NF-kB | VEGFR | ERK | PI3K | Akt | Tyrosinase | p38MAPK | GSK-3 | Antifection | TRP | Tyr
    In vitro:
    Molecules. 2014 Aug 4;19(8):11404-18.
    Analysis on blast fungus-responsive characters of a flavonoid phytoalexin sakuranetin; accumulation in infected rice leaves, antifungal activity and detoxification by fungus.[Pubmed: 25093982]
    To understand the role of the rice flavonoid phytoalexin (PA) Sakuranetin for blast resistance, the fungus-responsive characteristics were studied.
    METHODS AND RESULTS:
    Young rice leaves in a resistant line exhibited hypersensitive reaction (HR) within 3 days post inoculation (dpi) of a spore suspension, and an increase in Sakuranetin was detected at 3 dpi, increasing to 4-fold at 4 dpi. In the susceptible line, increased Sakuranetin was detected at 4 dpi, but not at 3 dpi, by which a large fungus mass has accumulated without HR. Induced expression of a PA biosynthesis gene OsNOMT for naringenin 7-O-methyltransferase was found before accumulation of Sakuranetin in both cultivars. The antifungal activity of Sakuranetin was considerably higher than that of the major rice diterpenoid PA momilactone A in vitro and in vivo under similar experimental conditions. The decrease and detoxification of Sakuranetin were detected in both solid and liquid mycelium cultures, and they took place slower than those of momilactone A. Estimated local concentration of Sakuranetin at HR lesions was thought to be effective for fungus restriction, while that at enlarged lesions in susceptible rice was insufficient.
    CONCLUSIONS:
    These results indicate possible involvement of Sakuranetin in blast resistance and its specific relation to blast fungus.
    Biochem Biophys Res Commun. 2008 Aug 8;372(4):835-9.
    Sakuranetin induces adipogenesis of 3T3-L1 cells through enhanced expression of PPARgamma2.[Pubmed: 18522800 ]
    Sakuranetin (5,4'-dihydroxy-7-methoxyflavone) belongs to the flavanone class of polyphenols predominantly known as phytoalexin in rice plant.
    METHODS AND RESULTS:
    In this study, we demonstrate that Sakuranetin strongly induces differentiation of 3T3-L1 preadipocytes, as evidenced by increased triglyceride accumulation and glycerol-3-phosphate dehydrogenase (GPDH) activity. In addition, even in the absence of adipogenic hormonal stimuli, Sakuranetin strongly induced adipogenesis and expression of genes that are critical for the adipocytes phenotype. Time-course analyses indicated that Sakuranetin induces PPARgamma2 expression without prior induction of C/EBPbeta, a transcriptional regulator of PPARgamma2 in adipogenesis. In 3T3-L1 preadipocytes, the transcriptional factors GATA-2 and GATA-3 are known to down-regulate adipogenesis by direct binding to the C/EBPbeta protein and to the GATA-binding site on the PPARgamma2 promoter. We found that Sakuranetin significantly reduced the expression of GATA-2. Moreover, we observed that Sakuranetin stimulated glucose uptake in differentiated 3T3-L1 adipocytes.
    CONCLUSIONS:
    These results suggest that Sakuranetin may contribute to maintain glucose homeostasis in animals.
    J. Food Sci., 2003, 68(68):52-6.
    Antimutagenic Activity of Sakuranetin from Prunus Jamasakura.[Reference: WebLink]
    Sakuranetin (compound 1) from bark of Prunus jamasakura showed a suppressive effect on umu gene expression of SOS response in Salmonella typhimurium TA1535/pSK1002 against the mutagen furylfuramide.
    METHODS AND RESULTS:
    Gene expression was suppressed 83% at a concentration of 0.70 μmol/mL. The ID50 value of compound 1 was 0.30 μmol/mL. This compound showed the suppression of 4NQO, MNNG, Trp-P-1, AfB1, activated Trp-P-1, and UV irradiation-induced SOS response. The methylated derivative (compound 2) of compound 1 showed less suppressive effect against all mutagens than compound 1. The antimutagenic activities of compounds 1 and 2 against furylfuramide, Trp-P-1, and activated Trp-P-1 were assayed by the Ames test using the S. typhimurium TA100 strain.
    In vivo:
    Acta Histochem. 2016 Jul;118(6):615-624.
    Sakuranetin reverses vascular peribronchial and lung parenchyma remodeling in a murine model of chronic allergic pulmonary inflammation.[Pubmed: 27425653 ]
    Asthma is a disease of high prevalence and morbidity that generates high costs in hospitalization and treatment. Although the airway is involved in the physiopathology of asthma, there is also evidence of the importance of vascular and lung parenchyma inflammation and remodeling, which can contribute to the functional pulmonary alterations observed in asthmatic patients. Our aim was to evaluate treatment using sakuranetin, a flavone isolated from the twigs of Baccharis retusa (Asteraceae), on vascular and lung parenchyma alterations in an experimental murine model of asthma.
    METHODS AND RESULTS:
    Male BALB/c mice were subjected to a sensitization protocol with ovalbumin for 30days and were treated with or without sakuranetin (20mg/kg/mice) or dexamethasone (5mg/kg/mice); then, the lungs were collected for histopathological analysis. We evaluated extracellular matrix remodeling (collagen and elastic fibers), inflammation (eosinophils and NF-kB) and oxidative stress (8-isoprostane) in the pulmonary vessels and lung parenchyma. The thickness of the vascular wall was quantified, as well as the vascular endothelial growth factor (VEGF) levels. We demonstrated that sakuranetin reduced the number of eosinophils and elastic fibers in both the pulmonary vessels and the lung parenchyma, probably due to a reduction of oxidative stress and of the transcription factor NF-kB and VEGF levels in the lung. In addition, it reduced the thickness of the pulmonary vascular wall. The treatment had no effect on the collagen fibers. In most of the parameters, the effect of sakuranetin was similar to the dexamethasone effect.
    CONCLUSIONS:
    Sakuranetin had anti-inflammatory and antioxidant effects, preventing vascular and distal parenchyma changes in this experimental model of asthma.
    Am J Physiol Lung Cell Mol Physiol . 2017 Feb 1;312(2):L217-L230.
    Prophylactic and therapeutic treatment with the flavonone sakuranetin ameliorates LPS-induced acute lung injury[Pubmed: 27881407]
    Abstract Sakuranetin is the main isolate flavonoid from Baccharis retusa (Asteraceae) leaves and exhibits anti-inflammatory and antioxidative activities. Acute respiratory distress syndrome is an acute failure of the respiratory system for which effective treatment is urgently necessary. This study investigated the preventive and therapeutic effects of sakuranetin on lipopolysaccharide (LPS)-induced acute lung injury (ALI) in mice. Animals were treated with intranasal sakuranetin 30 min before or 6 h after instillation of LPS. Twenty-four hours after ALI was induced, lung function, inflammation, macrophages population markers, collagen fiber deposition, the extent of oxidative stress, and the expression of matrix metalloprotease-9 (MMP-9), tissue inhibitor of MMP-9 (TIMP-1) and NF-κB were evaluated. The animals began to show lung alterations 6 h after LPS instillation, and these changes persisted until 24 h after LPS administration. Preventive and therapeutic treatment with sakuranetin reduced the neutrophils in the peripheral blood and in the bronchial alveolar lavage. Sakuranetin treatment also reduced macrophage populations, particularly that of M1-like macrophages. In addition, sakurnaetin treatment reduced keratinocyte-derived chemokines (IL-8 homolog) and NF-κB levels, collagen fiber formation, MMM-9 and TIMP-1-positive cells, and oxidative stress in lung tissues compared with LPS animals treated with vehicle. Finally, sakuranetin treatment also reduced total protein, and the levels of TNF-α and IL-1β in the lung. This study shows that sakuranetin prevented and reduced pulmonary inflammation induced by LPS. Because sakuranetin modulates oxidative stress, the NF-κB pathway, and lung function, it may constitute a novel therapeutic candidate to prevent and treat ALI. Keywords: LPS; acute lung injury; inflammation; sakuranetin.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.4928 mL 17.4642 mL 34.9284 mL 69.8568 mL 87.321 mL
    5 mM 0.6986 mL 3.4928 mL 6.9857 mL 13.9714 mL 17.4642 mL
    10 mM 0.3493 mL 1.7464 mL 3.4928 mL 6.9857 mL 8.7321 mL
    50 mM 0.0699 mL 0.3493 mL 0.6986 mL 1.3971 mL 1.7464 mL
    100 mM 0.0349 mL 0.1746 mL 0.3493 mL 0.6986 mL 0.8732 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
    4'-甲氧基黄烷酮; 4'-Methoxyflavanone CFN70492 97005-76-0 C16H14O3 = 254.3 5mg QQ客服:215959384
    甘草素; Liquiritigenin CFN99156 578-86-9 C15H12O4 = 256.25 20mg QQ客服:2056216494
    6,4'-Dihydroxy-7-methoxyflavanone; 6,4'-Dihydroxy-7-methoxyflavanone CFN89523 189689-32-5 C16H14O5 = 286.27 5mg QQ客服:1413575084
    Furano(2'',3'',7,6)-4'-hydroxyflavanone; Furano(2'',3'',7,6)-4'-hydroxyflavanone CFN96537 1454619-70-5 C17H12O4 = 280.27 5mg QQ客服:2159513211
    柚皮素; 4',5,7-三羟基黄烷酮; Naringenin CFN98742 480-41-1 C15H12O5 = 272.3 20mg QQ客服:1457312923
    4',7-二乙酸橘皮素酯; Naringenin-4',7-diacetate CFN99848 18196-13-9 C19H16O7 = 356.3 5mg QQ客服:2056216494
    三乙酸柚皮素酯; Naringenin triacetate CFN98603 3682-04-0 C21H18O8 = 398.4 5mg QQ客服:1413575084
    5-O-甲基柚皮素; 5-O-Methylnaringenin CFN97060 61775-19-7 C16H14O5 = 286.3 5mg QQ客服:1413575084
    樱花亭; Sakuranetin CFN98366 2957-21-3 C16H14O5 = 286.3 20mg QQ客服:2159513211
    异樱花亭; Isosakuranetin CFN98743 480-43-3 C16H14O5 = 286.3 20mg QQ客服:3257982914

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