Trifolirhizin

Trifolirhizin
Product Name Trifolirhizin
CAS No.: 6807-83-6
Catalog No.: CFN97160
Molecular Formula: C22H22O10
Molecular Weight: 446.4 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Cryst.
Targets: Adrenergic Receptor | COX | TNF-α | IL Receptor
Source: The roots of Sophora flavescens L.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price: $128/20mg
Trifolirhizin possesses potential anti-inflammatory and anti-cancer activities, it inhibits acetylcholine mediated airway smooth muscle (ASM) contraction or directly relaxes pre-contracted ASM independent of β 2 -adrenoceptors. Trifolirhizin may be a a candidate as skin-whitening agents, it exerts varying degrees of inhibition on tyrosinase-dependent melanin biosynthesis.
Inquire / Order: manager@chemfaces.com
Technical Inquiries: service@chemfaces.com
Tel: +86-27-84237783
Fax: +86-27-84254680

Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
  • J Ethnopharmacol. 2017 Feb 2;
  • Cell Physiol Biochem.2017;43(4):1425-1435.
  • Journal of Functional FoodsMarch 2017
  • Anticancer Res.2014 Jul;34(7):3505-9.
  • Journal of Life Science2017.2;
  • Mol Immunol. 2016 Oct;78:121-132.
  • PLoS One. 2015 May 15.
  • J Exp Bot. 2016 May 18.
  • Phytother Res.2015 Apr 17.
  • Braz J Med Biol Res. 2016 Jul 4;49(7).
  • Hematoxylin

    Catalog No: CFN96490
    CAS No: 517-28-2
    Price: $30/20mg
    3,9-Dihydroxypterocarpan

    Catalog No: CFN97043
    CAS No: 61135-91-9
    Price: Inquiry(manager@chemfaces.com)
    Isomedicarpin

    Catalog No: CFN97226
    CAS No: 74560-05-7
    Price: Inquiry(manager@chemfaces.com)
    Medicarpin

    Catalog No: CFN98411
    CAS No: 32383-76-9
    Price: $338/5mg
    Medicarpin 3-O-glucoside

    Catalog No: CFN89498
    CAS No: 52766-70-8
    Price: Inquiry(manager@chemfaces.com)
    Glycinol

    Catalog No: CFN95122
    CAS No: 69393-95-9
    Price: $398/5mg
    6alpha-Hydroxymedicarpin

    Catalog No: CFN96029
    CAS No: 61135-92-0
    Price: Inquiry(manager@chemfaces.com)
    Homopterocarpin

    Catalog No: CFN97720
    CAS No: 606-91-7
    Price: Inquiry(manager@chemfaces.com)
    (-)-Variabilin

    Catalog No: CFN97945
    CAS No: 370102-93-5
    Price: Inquiry(manager@chemfaces.com)
    Methylnissolin

    Catalog No: CFN90838
    CAS No: 733-40-4
    Price: $388/10mg
    J Agric Food Chem. 2009 Jun 10;57(11):4580-5.
    Anti-Inflammatory and antiproliferative activities of trifolirhizin, a flavonoid from Sophora flavescens roots.[Pubmed: 19402641 ]
    Trifolirhizin, a pterocarpan flavonoid, was isolated from the roots of Sophora flavescens, and its chemical structure was confirmed by (1)H and (13)C NMR and MS spectra.
    METHODS AND RESULTS:
    Its anti-inflammatory activity was examined in lipopolysaccharide (LPS)-stimulated mouse J774A.1 macrophages. Trifolirhizin not only dose-dependently inhibited LPS-induced expression of pro-inflammatory cytokines including tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) but also inhibited lipopolysaccharide (LPS)-induced expression of cyclooxygenase-2 (COX-2). In addition, Trifolirhizin showed in vitro inhibitory effects on the growth of human A2780 ovarian and H23 lung cancer cells.
    CONCLUSIONS:
    These results suggest that Trifolirhizin possesses potential anti-inflammatory and anticancer activities.
    Biol Pharm Bull. 2008 Jan;31(1):154-8.
    Inhibitory effects of kurarinol, kuraridinol, and trifolirhizin from Sophora flavescens on tyrosinase and melanin synthesis.[Pubmed: 18175961]
    Previously, it was reported that some prenylated flavonoids contained in the dichloromethane fraction of the ethanolic extract of Sophora flavescens, such as kuraridin, sophoraflavanone G, kurarinone, and kushenol F, are tyrosinase inhibitors; however, based on the level of these inhibitors in the extract, its inhibitory effect on tyrosinase activity was higher than expected. This has led us to further investigate other possible constituents that may contribute to the extract's strong inhibitory activity.
    METHODS AND RESULTS:
    The results of this study indicate that kurarinol (1), kuraridinol (2), and Trifolirhizin (3), from the ethyl acetate fraction of Sophora extract, can inhibit tyrosinase activity. Compared with kojic acid (16.22+/-1.71 microM), compounds 1-3 possessed potent tyrosinase inhibitory activity with IC(50) values of 8.60+/-0.51, 0.88+/-0.06, and 506.77+/-4.94 microM, respectively. These three compounds were further tested for their inhibitory effects on melanogenesis. In cultured B16 melanoma cells, 1-3 markedly inhibited (>50%) melanin synthesis at 50 microM.
    CONCLUSIONS:
    This is the first study indicating that 1-3 exert varying degrees of inhibition on tyrosinase-dependent melanin biosynthesis, and therefore, are candidates as skin-whitening agents.
    Oncol Rep. 2004 Dec;12(6):1183-8.
    Induction of apoptosis by maackiain and trifolirhizin (maackiain glycoside) isolated from sanzukon (Sophora Subprostrate Chen et T. Chen) in human promyelotic leukemia HL-60 cells.[Pubmed: 15547735 ]
    We have investigated the effects of maackiain and Trifolirhizin (maackiain glycoside) isolated from sanzukon (Sophora Subprostrate Chen et T. Chen) on DNA of human promyelotic HL-60 leukemia cells.
    METHODS AND RESULTS:
    It was found that extent of induction of apoptosis by maackiain was larger than that by Trifolirhizin in human leukemia HL-60 cells. Morphological changes showing apoptotic bodies were observed in the HL-60 cells treated with maackiain and Trifolirhizin. The fragmentations of DNA by maackiain and Trifolirhizin to oligonucleosomal-sized fragments that is a characteristic of apoptosis was observed to be concentration- and time-dependent in the HL-60 cells.
    CONCLUSIONS:
    The data of the present study show that the suppressions by maackiain and trifolrhizin of growth of the HL-60 cells result from the induction of apoptosis by these compounds, and that the extent of growth suppression and induction of apoptosis by maackiain was greater than that by the glycoside (Trifolirhizin).
    Phytochemistry. 2013 Nov;95:259-67.
    The Sophora flavescens flavonoid compound trifolirhizin inhibits acetylcholine induced airway smooth muscle contraction.[Pubmed: 23993294]
    Asthma is a serious health problem worldwide, particularly in industrialized countries. Despite a better understanding of the pathophysiology of asthma, there are still considerable gaps in knowledge as well as a need for classes of drugs. ASHMI™ (Anti-asthma Herbal Medicine Intervention) is an aqueous extract of Ganoderma lucidum (Fr.) P. Karst (Ling Zhi), Sophora flavescens Aiton (Ku Shen) and Glycyrrhiza uralensis Fisch. ex DC (Gan Cao).
    METHODS AND RESULTS:
    It prevents allergic asthma airway hyper-reactivity in mice and inhibits acetylcholine (ACh) induced airway smooth muscle (ASM) contraction in tracheal rings from allergic asthmatic mice. The purpose of this research was to identify individual herb(s) and their active compound(s) that inhibit ASM contraction. It was found that S. flavescens, but not G. lucidum or G. uralensis aqueous extracts, inhibited ASM contraction in tracheal rings from asthmatic mice.
    CONCLUSIONS:
    Bioassay-guided isolation and identification of flavonoid fractions/compound(s) via methylene chloride extraction, preparative HPLC fractionation, and LC-MS and NMR spectroscopic analyses showed that Trifolirhizin is an active constituent that inhibits acetylcholine mediated ASM contraction or directly relaxes pre-contracted ASM independent of β2-adrenoceptors.
    Isochlorogenic acid C

    Catalog No: CFN99120
    CAS No: 32451-88-0
    Price: $100/20mg
    Fargesin

    Catalog No: CFN98174
    CAS No: 31008-19-2
    Price: $128/20mg
    6-Methoxywogonin

    Catalog No: CFN98403
    CAS No: 3162-45-6
    Price: $368/5mg
    Picrasidine Q

    Catalog No: CFN92205
    CAS No: 101219-61-8
    Price: $388/10mg
    Ganoderic acid G

    Catalog No: CFN90801
    CAS No: 98665-22-6
    Price: $400/10mg
    Parishin A

    Catalog No: CFN93112
    CAS No: 62499-28-9
    Price: $120/20mg
    Secologanic acid

    Catalog No: CFN95028
    CAS No: 60077-46-5
    Price: $318/10mg
    20-O-Glucoginsenoside Rf

    Catalog No: CFN95036
    CAS No: 68406-27-9
    Price: $368/10mg
    Gancaonin N

    Catalog No: CFN95066
    CAS No: 129145-52-4
    Price: $463/5mg
    6''-O-acetylsaikosaponin A

    Catalog No: CFN95086
    CAS No: 64340-46-1
    Price: $268/10mg