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    Natural Products
    Mulberrin
    Information
    CAS No. 62949-79-5 Price $288 / 20mg
    Catalog No.CFN97085Purity>=98%
    Molecular Weight422.5 Type of CompoundFlavonoids
    FormulaC25H26O6Physical DescriptionYellow powder
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    * Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
    According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
    Size /Price /Stock 10 mM * 1 mL in DMSO / $121.7 / In-stock
    Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
    Our products had been exported to the following research institutions and universities, And still growing.
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  • Package
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    Mulberrin

    Mulberrin
    Product Name Mulberrin
    CAS No.: 62949-79-5
    Catalog No.: CFN97085
    Molecular Formula: C25H26O6
    Molecular Weight: 422.5 g/mol
    Purity: >=98%
    Type of Compound: Flavonoids
    Physical Desc.: Yellow powder
    Targets: HIV | OATP2B1
    Source: The root barks of Morus alba L.
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price: $288 / 20mg
    Inquire / Order: manager@chemfaces.com
    Technical Inquiries: service@chemfaces.com
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    Fax: +86-27-84254680

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    1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
  • Pharmacogn Mag.2015, 11:S585-91
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  • Sci Rep. 2017, 17332(7)
  • J Nat Med.2020, 74(3):550-560.
  • Biomolecules.2020, 10(6):925.
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  • Korean Journal of Pharmacognosy2018, 49(3):270-277
  • Ann Transl Med.2019, 7(23):731
  • LWT2020, 130:109535
  • Related Screening Libraries
    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
    10 mM * 1 mL in DMSO / Inquiry / In-stock
    Related Libraries
  • Antiviral Compound Library
  • Antihyperglycemic Compound Library
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  • HIV Inhibitor Library
  • Biological Activity
    Description: Mulberrin is a strong inhibitor of organic anion-transporting polypeptide 2B1 (OATP2B1)-mediated estrone-3-sulfate (E3S) uptake with an IC50 value being 1.8 ±1.5 μM; it also as HIV-1 reverse transcriptase inhibitor. Mulberrin has significantly reduced role on blood sugar of type II diabetes model of rats.
    Targets: HIV | OATP2B1
    In vitro:
    Bioinformation. 2012;8(24):1206-10.
    Virtual screening of Indonesian herbal database as HIV-1 reverse transcriptase inhibitor.[Pubmed: 23275721]
    HIV-1 (Human immunodeficiency virus type 1) is a member of retrovirus family that could infect human and causing AIDS disease. AIDS epidemic is one of most destructive diseases in modern era. There were more than 33 million people infected by HIV until 2010. Various studies have been widely employed to design drugs that target the essential enzymes of HIV-1 that is, reverse transcriptase, protease and integrase.
    METHODS AND RESULTS:
    In this study, in silico virtual screening approach is used to find lead molecules from the library or database of natural compounds as HIV-1 reverse transcriptase inhibitor. Virtual screening against Indonesian Herbal Database using AutoDock4 performed on HIV-1 reverse transcriptase.
    CONCLUSIONS:
    From the virtual screening, top ten compounds were Mulberrin, plucheoside A, vitexilactone, brucine N-oxide, cyanidin 3-arabinoside, alpha-mangostin, guaijaverin, erycristagallin, morusin and sanggenol N.
    In vivo:
    Journal of Traditional Chinese Medicine University of Hunan, 2011, 31(5):26-8.
    Experimental study of mulberrin on blood glucose of Type Ⅱ diabetes model rats.[Reference: WebLink]
    The experiment had investigated the results by using Mulberrin on blood glucose,insulin,glycated hemoglobin,glucose tolerance of Type II diabetes model rats.
    METHODS AND RESULTS:
    According to Chinese herbal medicine research guide(oral) pharmacodynamics experiment demands,choose the normal mice(KM mice),spontaneous diabetic mice(NOD mice) and chain fosomycin heightening urea to heat feed type II diabetes rats,fill the stomach give different doses of mulberry element,research on the blood glucose,insulin,glycated hemoglobin influence.1.The concentration of blood glucose of regular lab rats has no visibly changed(P0.05)after using Mulberrin of 50.0,25.0,12.5 mg/kg by oral administration for 14 days.By contrast,the blood glucose were obviously lower and rates of Insulin were obviously higher(P0.05) in NOD rats.2.The concentration of blood glucose of has reduced obviously after using Mulberrin of 30.0,15.0,7.5 mg/kg).Compare with the regular group,the rates of Insulin and Glycosylated Hemoglobin were obviously lower(P0.05) after using Mulberrin of 30,15 mg/kg by oral administration for 14 days.
    CONCLUSIONS:
    Mulberrin has significantly reduced role on blood sugar of type II diabetes model of rats.
    Mulberrin Description
    Source: The root barks of Morus alba L.
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Storage: 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

    After receiving: 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.
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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.3669 mL 11.8343 mL 23.6686 mL 47.3373 mL 59.1716 mL
    5 mM 0.4734 mL 2.3669 mL 4.7337 mL 9.4675 mL 11.8343 mL
    10 mM 0.2367 mL 1.1834 mL 2.3669 mL 4.7337 mL 5.9172 mL
    50 mM 0.0473 mL 0.2367 mL 0.4734 mL 0.9467 mL 1.1834 mL
    100 mM 0.0237 mL 0.1183 mL 0.2367 mL 0.4734 mL 0.5917 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.
    Protocol
    Kinase Assay:
    Pharm Biol. 2016;54(2):293-302.
    Identification of natural products as modulators of OATP2B1 using LC-MS/MS to quantify OATP-mediated uptake.[Pubmed: 25858254 ]
    Organic anion-transporting polypeptide 2B1 (OATP2B1) which is highly expressed in enterocytes and hepatocytes could be a key determinant for the intestinal absorption and hepatic uptake of its substrate drugs. Natural products are commonly used in traditional Chinese medicine, foods, and beverages. The objective of this study is to determine the OATP2B1-mediated drug interactions that could occur between natural products and OATP2B1 substrate drugs.
    METHODS AND RESULTS:
    Human OATP2B1 was transiently expressed in human embryonic kidney (HEK293) cells and characterized by immunofluorescence, Western blot, and uptake assay. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods for detecting OATP2B1 substrates estrone-3-sulfate (E3S) and three statins had been developed and were employed to investigate the effects of 27 frequently used natural products on the function of OATP2B1. Uptake of 5 μM E3S and 1 μM statins in the absence or presence of natural products was measured at 37 °C for 2 min with empty vector- and OATP2B1-transfected HEK293 cells. The IC50 values of inhibitors for OATP2B1-mediated 5 μM E3S uptake were determined. Our results showed that Mulberrin, scutellarin, quercetin, and glycyrrhetinic acid were strong inhibitors of OATP2B1-mediate E3S uptake with IC50 values being 1.8, 2.0, 7.5, and 13.0 μM, which were comparable with their plasma concentrations in clinical trials. They also inhibited OATP-mediated uptake of atorvastatin, fluvastatin, and rosuvastatin. These results indicated that clinically relevant drug interactions could occur between these natural compounds and OATP2B1 substrate drugs.
    CONCLUSIONS:
    The information obtained from this study might be helpful to predict and to avoid potential OATP2B1-mediated drug interactions.
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