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  • 雏菊叶龙胆酮

    Bellidifolin

    雏菊叶龙胆酮
    产品编号 CFN89132
    CAS编号 2798-25-6
    分子式 = 分子量 C14H10O6 = 274.22
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Xanthones
    植物来源 The plants of Gentiana species.
    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
    雏菊叶龙胆酮 CFN89132 2798-25-6 1mg QQ客服:1457312923
    雏菊叶龙胆酮 CFN89132 2798-25-6 5mg QQ客服:1457312923
    雏菊叶龙胆酮 CFN89132 2798-25-6 10mg QQ客服:1457312923
    雏菊叶龙胆酮 CFN89132 2798-25-6 20mg QQ客服:1457312923
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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 Fribourg (Switzerland)
  • Universiti Malaysia Pahang (Malaysia)
  • Melbourne University (Australia)
  • Martin Luther University of Halle-Wittenberg (Germany)
  • University of Queensland (Australia)
  • University of East Anglia (United Kingdom)
  • Universidade Católica Portuguesa (Portugal)
  • Uniwersytet Jagielloński w Krakowie (Poland)
  • Aarhus University (Denmark)
  • Weizmann Institute of Science (Israel)
  • Anna University (India)
  • University of Medicine and Pharmacy (Romania)
  • University of Pretoria (South Africa)
  • University of Zurich (Switzerland)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Biol Pharm Bull.2020, 43(10):1534-1541.
  • Appl. Sci. 2021, 11(8),3437.
  • J Nat Med.2020, 74(1):65-75
  • Planta Med.2019, 85(9-10):766-773
  • Journal of Food and Drug Analysis2023, 31(3), 9.
  • Front Cell Dev Biol.2021, 9:588093.
  • Nat Prod Sci.2018, 24(2):109-114
  • Phytother Res.2018, 32(12):2551-2559
  • Toxicol Appl Pharmacol.2022, 434:115815.
  • BMC Complement Med Ther.2023, 23(1):264.
  • Chem Res Toxicol.2023, 36(2):213-229.
  • Pharmaceuticals (Basel). 2021, 14(10):986.
  • J Nat Prod.2019, 82(4):1002-1008
  • J of App. Res. on Med&Aromatic Plants2020, 100291.
  • BMC Plant Biol.2018, 18(1):122
  • Int J Immunopathol Pharmacol.2019, 33:2058738419857537
  • Journal of Plant Growth Regulation2022, 10705-2.
  • Microorganisms.2021, 9(12):2514.
  • Cancers (Basel).2023, 15(1):37.
  • J AOAC Int.2021, 104(6):1634-1651.
  • Plant Cell Tiss Org2020, 1-16
  • J Med Food.2021, 24(3):209-217.
  • Anat Rec (Hoboken).2021, 304(2):323-332.
  • ...
  • 生物活性
    Description: Bellidifolin has anti-oxidation, hepatoprotective, anti-inflammatory and antitumor actions, it may contribute to the protective effects associated with nerve injury initiated by hypoxia by mechanisms related to inhibition of cell apoptosis independent of the ERK pathway. Bellidifolin shows interesting inhibitory activity of monoamine oxidases (MAO) A, it could be useful for treating type-2 diabetes, likely via the improvement of insulin resistance (IR). Bellidifolin also shows an antifungal effect (MIC values of 50 microg/mL).
    Targets: ERK | p38MAPK | Caspase | ROS | PI3K | LDL | MAO
    In vitro:
    J Ethnopharmacol. 2014 May 14;153(3):854-63.
    Two xanthones from Swertia punicea with hepatoprotective activities in vitro and in vivo.[Pubmed: 24690777 ]
    Swertia punicea Hemsl. (Gentianaceae) is more commonly known as "Ganyan-cao" and used mainly as a traditional Chinese folk medicine for the treatment of acute bilious hepatitis, cholecystitis, fever, intoxification and jaundice.
    METHODS AND RESULTS:
    The active hepatoprotective constituents of Swertia punicea were purified using various column chromatography techniques. The structures of two isolated compounds were determined on the basis of spectroscopic data interpretation such as NMR analysis. The hepatoprotective activities of isolated compounds were evaluated by using hepatotoxicity in vitro and dimethylnitrosamine-induced rat hepatic fibrosis in vivo, respectively. Two xanthones, 1, 7-dihydroxy-3, 4, 8-trimethoxyxanthone (1) and bellidifolin (2) were isolated from the stems of Swertia punicea. The compounds 1 and 2 exhibited notable hepatoprotective activities against carbon tetrachloride (CCl4) -induced HepG2 cell damage, and effectively alleviated the levels of aspartate transaminase (AST), lactate dehydrogenase (LDH), superoxide dismutase (SOD) and malonic dialdehyde (MDA) induced by CCl₄ in a concentration-dependent manner. Co-treatment with compound 2 significantly increased the cell viability compared with N-acetyl-p-aminophenol (APAP) treatment. Compound 2 also alleviated APAP-induced hepatotoxicity by increasing glutathione (GSH) content and decreasing hydroxyl free radical (·OH) levels and reactive oxygen specises (ROS) production. In addition, the protective effect of compound 1 significantly alleviated DMN-induced liver inflammation and fibrosis. Oral administration of compound 1 recovered the reduction of albumin (ALB) and reversed the elevation of serum alanine transaminase (ALT), AST and total bilirubin (TBIL) in dimethylnitrosamine (DMN)-induced fibrotic rats. Severe oxidative stress induced in fibrotic rats was evidenced by a 1.5-fold elevation in MDA and a fall in the SOD activity, and treatment with compound 1 protected against these adverse effects. Recovery of rat liver tissue against DMN-induced hepatocellular necrosis, inflammatory changes and hepatic fibrosis by compound 1 is also confirmed by H&E and Masson stained histopathological evaluation of liver tissue.
    CONCLUSIONS:
    Two xanthones from Swertia punicea exhibited hepatoprotective activities in vitro (compounds 1 and 2) and in vivo (compound 1), respectively.
    Z Naturforsch C. 2012 Jan-Feb;67(1-2):29-38.
    Antimicrobial and antioxidant activities of Gentianella multicaulis collected on the Andean Slopes of San Juan Province, Argentina.[Pubmed: 22486039]
    The infusion of the aerial parts of Gentianella multicaulis (Gillies ex Griseb.) Fabris (Gentianaceae), locally known as 'nencia', is used in San Juan Province, Argentina, as stomachic and as a bitter tonic against digestive and liver problems.
    METHODS AND RESULTS:
    The bioassay-guided isolation of G. multicaulis extracts and structural elucidation of the main compounds responsible for the antifungal and free radical scavenging activities were performed. The extracts had strong free radical scavenging effects in the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay (45-93% at 10 microg/mL) and ferric-reducing antioxidant power (FRAP) assay at 200 microg/mL. Demethylbellidifolin (4) had high antioxidant activity in the DPPH and FRAP assay. The dermatophytes Microsporum gypseum, Trichophyton mentagrophytes, and T. rubrum were moderately inhibited by the different extracts (MIC values of 125-250 microg/mL). Demethylbellidifolin (4), bellidifolin (5), and isobellidifolin (6) showed an antifungal effect (MIC values of 50 microg/mL), while swerchirin (3) was less active with a MIC value of 100 microg/mL. In addition, oleanolic acid (1) and ursolic acid (2) were also isolated.
    CONCLUSIONS:
    These findings demonstrate that Gentianella multicaulis collected in the mountains of the Province of San Juan, Argentina, is an important source of compounds with antifungal and antioxidant activities.
    In vivo:
    Phytomedicine. 2010 Jun;17(7):533-9.
    Anti-diabetic effect of methylswertianin and bellidifolin from Swertia punicea Hemsl. and its potential mechanism.[Pubmed: 19962285 ]

    METHODS AND RESULTS:
    In this study, we continued to investigate the hypoglycemic activity of Swertia punicea Helmsl., the hypoglycemic and hypolipidemic effects of methylswertianin and bellidifolin from the active ethyl acetate (EtOAc) fraction, and the potential mechanism(s) underlying the improvement of insulin resistance. Streptozotocin (STZ)-induced type 2 diabetic male BABL/c mice treated with methylswertianin and bellidifolin at different doses (orally, 200 and 100mg/kg body wt./day) for 4 weeks were analyzed in comparison to untreated mice. The results proved that methylswertianin and bellidifolin significantly reduced fasting blood glucose (FBG). The administration of both compounds also improved the oral glucose tolerance and lowered fasting serum insulin (FINS). Moreover, post-administration evaluation revealed lower serum total cholesterol (TC), low density lipoprotein cholesterol (LDL) and triglyceride (TG) levels and increased relative high density lipoprotein cholesterol (HDL) concentrations (HDL/TC). Methylswertianin and bellidifolin appeared to improve insulin resistance by enhancing insulin signaling. The expression levels of insulin-receptor alpha subunit (InsR-alpha), insulin-receptor substrate-1 (IRS-1), and phosphatidylinositol 3-kinase (PI3K) were also increased after administration. Meanwhile, methylswertianin and bellidifolin increased hepatic glycogen content, decreased glucokinase (GK) activities and increased glucose-6-phosphatase (G6Pase) activities.
    CONCLUSIONS:
    In conclusion, these result indicated that methylswertianin and bellidifolin could be useful for treating type-2 diabetes, likely via the improvement of insulin resistance (IR).
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.6467 mL 18.2335 mL 36.4671 mL 72.9341 mL 91.1677 mL
    5 mM 0.7293 mL 3.6467 mL 7.2934 mL 14.5868 mL 18.2335 mL
    10 mM 0.3647 mL 1.8234 mL 3.6467 mL 7.2934 mL 9.1168 mL
    50 mM 0.0729 mL 0.3647 mL 0.7293 mL 1.4587 mL 1.8234 mL
    100 mM 0.0365 mL 0.1823 mL 0.3647 mL 0.7293 mL 0.9117 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
    Montixanthone; Montixanthone CFN91903 876305-36-1 C14H10O6 = 274.23 5mg QQ客服:2056216494
    3,6-二羟基-1,7-二甲氧基呫吨酮; 3,6-Dihydroxy-1,7-dimethoxyxanthone CFN89303 262292-34-2 C15H12O6 = 288.25 5mg QQ客服:2056216494
    Onjixanthone II; Onjixanthone II CFN89276 136083-93-7 C15H12O7 = 304.25 5mg QQ客服:2056216494
    6-羟基-1,2,3,7-四甲氧基咕吨酮; 6-Hydroxy-1,2,3,7-tetramethoxyxanthone CFN89282 64756-87-2 C17H16O7 = 332.30 5mg QQ客服:215959384
    1,2,3,6,7-Pentamethoxyxanthone; 1,2,3,6,7-Pentamethoxyxanthone CFN89241 64756-86-1 C18H18O7 = 346.33 5mg QQ客服:2056216494
    狭花马钱碱 A; Angustin A CFN89373 1415795-50-4 C16H14O7 = 318.27 5mg QQ客服:2159513211
    狭花马钱碱 B; Angustin B CFN89374 1415795-51-5 C17H16O7 = 332.30 5mg QQ客服:3257982914
    7,8,9-Trimethoxy-10H-1,3-dioxolo[4,5-b]xanthen-10-one; 7,8,9-Trimethoxy-10H-1,3-dioxolo[4,5-b]xanthen-10-one CFN98533 24562-58-1 C17H14O7 = 330.29 5mg QQ客服:1413575084
    1,5,6-Trihydroxy-3,7-dimethoxyxanthone ; 1,5,6-Trihydroxy-3,7-dimethoxyxanthone CFN89047 65008-02-8 C15H12O7 = 304.25 5mg QQ客服:1457312923
    1,5,6-三羟基双苯吡酮; 1,5,6-Trihydroxyxanthone CFN89364 5042-03-5 C13H8O5 = 244.19 5mg QQ客服:1457312923

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