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  • 橙黄决明素

    Aurantio-obtusin

    橙黄决明素
    产品编号 CFN99732
    CAS编号 67979-25-3
    分子式 = 分子量 C17H14O7 = 330.29
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Anthraquinones
    植物来源 The seeds of Cassia obtusifolia 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
    提供自定义包装
    产品名称 产品编号 CAS编号 包装 QQ客服
    橙黄决明素 CFN99732 67979-25-3 10mg QQ客服:1413575084
    橙黄决明素 CFN99732 67979-25-3 20mg QQ客服:1413575084
    橙黄决明素 CFN99732 67979-25-3 50mg QQ客服:1413575084
    橙黄决明素 CFN99732 67979-25-3 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
  • Deutsches Krebsforschungszentrum (Germany)
  • University of Oslo (Norway)
  • Universidad Miguel Hernández (Spain)
  • University of Wollongong (Australia)
  • Florida International University (USA)
  • University of South Australia (Australia)
  • Florida A&M University (USA)
  • Monash University Sunway Campus (Malaysia)
  • Universit?t Basel (Switzerland)
  • Sapienza University of Rome (Italy)
  • Lodz University of Technology (Poland)
  • National Chung Hsing University (Taiwan)
  • Center for protein Engineering (CIP) (Belgium)
  • The Vancouver Prostate Centre (VPC) (Canada)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Mol Divers.2022, s11030-022-10586-3.
  • Food Science and Biotechnology2015, 2205-2212
  • Molecules.2017, 22(11)
  • The Korea Journal of Herbology2020, 35(3):33-45.
  • Evid Based Complement Alternat Med.2021, 2021:6687513.
  • J Clin Med.2022, 11(13):3662.
  • Evid Based Complement Alternat Med.2022, 2022:1307173.
  • Food and Fermentation Industries2019, 45(7):45-51
  • Chem Biol Interact.2018, 283:59-74
  • J Hematol Oncol.2018, 11(1):112
  • Green Chemistry2021, ISSUE 2.
  • Plants (Basel).2022, 11(21):2947.
  • Evid Based Complement Alternat Med.2018, 2018:1073509
  • J Ethnopharmacol.2017, 197:157-164
  • Front Pharmacol.2023, 14:1244655.
  • J Chromatogr B Analyt Technol Biomed Life Sci.2021, 1187:123012.
  • Sci Rep.2019, 9(1):6429
  • J Appl Toxicol.2020, 40(7):965-978.
  • Front Immunol. 2020, 11:62.
  • Int J Med Sci.2021, 18(10):2155-2161.
  • Molecules.2021, 26(19):6032.
  • J Korean Med Obes Res.2023, 23:10-7
  • GENENCELL2023, 25:4356740
  • ...
  • 生物活性
    Description: Aurantio-obtusin possesses anti-allergic, vasorelaxation, hypotensive and hypolipidemic effects, it is a promising osteoanabolic compound with potential therapeutic applications in the prevention of osteoporosis and other metabolic bone diseases. Aurantio-obtusin can inhibit allergic responses in IgE-mediated mast cells and anaphylactic models, it suppresses degranulation, histamine production, and reactive oxygen species generation and inhibits the production and mRNA expression of tumor necrosis factor-α and interleukin-4, and also suppresses the prostaglandin E2 production and expression of cyclooxygenase 2.
    Targets: TNF-α | NO | Akt | NOS | PI3K | Serine | COX | ROS | PGE | IL Receptor
    In vitro:
    J Agric Food Chem. 2015 Oct 21;63(41):9037-46.
    Cassia tora Seed Extract and Its Active Compound Aurantio-obtusin Inhibit Allergic Responses in IgE-Mediated Mast Cells and Anaphylactic Models.[Pubmed: 26434611 ]
    Cassia tora seed is widely used due to its various biological properties including anticancer, antidiabetic, and anti-inflammatory effects. However, there has been no report of the effects of C. tora seed extract (CTE) on immunoglobulin E (IgE)-mediated allergic responses.
    METHODS AND RESULTS:
    In this research, we demonstrated the effects of CTE and its active compound aurantio-obtusin on IgE-sensitized allergic reactions in mast cells and passive cutaneous anaphylaxis (PCA). CTE and aurantio-obtusin suppressed degranulation, histamine production, and reactive oxygen species generation and inhibited the production and mRNA expression of tumor necrosis factor-α and interleukin-4. CTE and aurantio-obtusin also suppressed the prostaglandin E2 production and expression of cyclooxygenase 2. Furthermore, CTE and aurantio-obtusin suppressed IgE-mediated FcεRI signaling such as phosphorylation of Syk, protein kinase Cμ, phospholipase Cγ, and extracellular signal-regulated kinases. CTE and aurantio-obtusin blocked mast cell-dependent PCA in IgE-mediated mice.
    CONCLUSIONS:
    These results suggest that CTE and aurantio-obtusin are a beneficial treatment for allergy-related diseases.
    Planta Med. 2014 May;80(7):544-9.
    Aurantio-obtusin stimulates chemotactic migration and differentiation of MC3T3-E1 osteoblast cells.[Pubmed: 24841966]
    Osteoporosis is one of the major metabolic bone diseases and is among the most challenging noncommunicable diseases to treat. Although there is an increasing interest in identifying bioactive molecules for the prevention and management of osteoporosis, such studies principally focus only on differentiation and mineralization of osteoblasts or inhibition of osteoclast activity. Stimulation of osteoblast migration must be a promising osteoanabolic strategy for improved metabolic bone disease therapy.
    METHODS AND RESULTS:
    In this study, we show that an anthraquinone derivative, Aurantio-obtusin, stimulated chemotactic migration of MC3T3-E1 osteoblast cells in a concentration-dependent manner. The use of a real-time chemotaxis analyzing system, TAXIScan, facilitated the evaluation of both velocity and directionality of osteoblast migration in response to the compound. Besides migration, the compound stimulated osteoblast differentiation and mineralization.
    CONCLUSIONS:
    Taken together, the data presented in this paper demonstrate that Aurantio-obtusin is a promising osteoanabolic compound of natural origin with potential therapeutic applications in the prevention of osteoporosis and other metabolic bone diseases.
    2018 Nov 27;23(12):3093.
    Anti-Inflammatory Effects of Aurantio-Obtusin from Seed of Cassia obtusifolia L. through Modulation of the NF-κB Pathway[Pubmed: 30486383]
    Abstract Aurantio-obtusin, an anthraquinone compound, isolated from dried seeds of Cassia obtusifolia L. (syn. Senna obtusifolia; Fabaceae) and Cassia tora L. (syn. Senna tora). Although the biological activities of Semen Cassiae have been reported, the anti-inflammatory mechanism of aurantio-obtusin, its main compound, on RAW264.7 cells, remained unknown. We investigated the anti-inflammatory effect of aurantio-obtusin on lipopolysaccharide- (LPS)-induced RAW264.7 cells in vitro and elucidated the possible underlying molecular mechanisms. Nitric oxide production (NO) and prostaglandin E₂ (PGE₂) were measured by the Griess colorimetric method and enzyme-linked immunosorbent assay (ELISA), respectively. Protein expression levels of cyclooxygenase 2 (COX-2) were monitored by cell-based ELISA. Interleukin 6 (IL-6) and tumor necrosis factor-alpha (TNF-α) synthesis were analyzed using ELISA. The mRNA expression of nitric oxide synthase (iNOS), COX-2, and the critical pro-inflammatory cytokines (IL-6 and TNF-α) were detected by quantitative real-time PCR. Aurantio-obtusin significantly decreased the production of NO, PGE₂, and inhibited the protein expression of COX-2, TNF-α and IL-6, which were similar to those gene expression of iNOS, COX-2, TNF-α and IL-6 (p < 0.01). Consistent with the pro-inflammatory gene expression, the Aurantio-obtusin efficiently reduced the LPS-induced activation of nuclear factor-κB in RAW264.7 cells. These results suggested that aurantio-obtusin may function as a therapeutic agent and can be considered in the further development of treatments for a variety of inflammatory diseases. Further studies may provide scientific evidence for the use of aurantio-obstusin as a new therapeutic agent for inflammation-related diseases.
    In vivo:
    Journal of Analytical Science,2016, 32(2):178-82.
    Metabolomics-based Study of the Lipid Regulating Effect of Aurantio-obtusin on Hyperlipidemia Rats.[Reference: WebLink]
    The influences of Aurantio-obtusin on endogenous metabolites in blood of hyperlipemia rats were investigated by metabonomics method in order to find the related biomarkers.
    METHODS AND RESULTS:
    The rat model was established by hyperlipidemia rats that were raised by high fat diet and then treated with intragastric administration of Aurantio-obtusin.Metabolites in plasma of hyperlipidemia rats were accurately analyzed by gas chromatography-mass spectrometry.In order to find out the potential biomarkers,principal component analysis,partial least squares discriminant analysis and random forest algorithm were used to study the changes of endogenous metabolite profiles in rats before modeling after modeling and after drug treatments.Ten potential biomarkers were obtained as the final achievement:alanine,glycine,valine,isoleucine,fumaric acid,serine,1,5-anhydro-D-ghlcitol,linoleic acid,stearic acid and cholesterol.
    CONCLUSIONS:
    This investigation demonstrates that aurantio has a good lipid regulating effect mainly by affecting the body amino acid and fatty acid metabolism.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.0276 mL 15.1382 mL 30.2764 mL 60.5528 mL 75.6911 mL
    5 mM 0.6055 mL 3.0276 mL 6.0553 mL 12.1106 mL 15.1382 mL
    10 mM 0.3028 mL 1.5138 mL 3.0276 mL 6.0553 mL 7.5691 mL
    50 mM 0.0606 mL 0.3028 mL 0.6055 mL 1.2111 mL 1.5138 mL
    100 mM 0.0303 mL 0.1514 mL 0.3028 mL 0.6055 mL 0.7569 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
    决明蒽醌; 美决明子素; Obtusifolin CFN90394 477-85-0 C16H12O5 = 284.27 20mg QQ客服:215959384
    6-羟基茜草素; 6-Hydroxyrubiadin CFN97444 87686-86-0 C15H10O5 = 270.2 5mg QQ客服:2159513211
    乳癖蒽醌; 2-甲基-3,6-二羟基-1-甲氧基-9,10-蒽醌; Rubianthraquinone CFN96569 644967-44-2 C16H12O5 = 284.26 5mg QQ客服:2159513211
    3-羟基巴戟醌; 3-hydroxymorindone CFN80104 80368-74-7 C15H10O6 = 286.24 10mg QQ客服:3257982914
    芦荟大黄素; Aloeemodin CFN98749 481-72-1 C15H10O5 = 270.2 20mg QQ客服:2159513211
    羟基大黄素; Citreorosein CFN98750 481-73-2 C15H10O6 = 286.2 5mg QQ客服:215959384
    2-羟基-1,5-二甲氧基-6-(甲氧基甲基)-9,10- 蒽二酮; 1,5,15-Tri-O-methylmorindol CFN97518 942609-65-6 C18H16O6 = 328.3 5mg QQ客服:2159513211
    橙黄决明素; Aurantio-obtusin CFN99732 67979-25-3 C17H14O7 = 330.29 20mg QQ客服:1413575084
    决明素; Obtusin CFN93032 70588-05-5 C18H16O7 = 344.31 5mg QQ客服:1457312923
    黄决明素; Chrysoobtusin CFN91661 70588-06-6 C19H18O7 = 358.34 5mg QQ客服:1457312923

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