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    CAS No. 16625-57-3 Price
    Catalog No.CFN96081Purity>=98%
    Molecular Weight295.4Type of CompoundAlkaloids
    FormulaC19H21NO2Physical DescriptionOil
    Download     COA    MSDSSimilar structuralComparison (Web)
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    Featured Products
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    Polygalaxanthone III

    Catalog No: CFN90208
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    Biological Activity
    Description: 1. Argentinine exhibits significant activity against Trypanosoma cruzi.
    Targets: Antifection
    Argentinine Description
    Source: The herbs of Piper longum
    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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    Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.

    PMID: 29328914

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.

    PMID: 29149595

    Scientific Reports 2017 Dec 11;7(1):17332.
    doi: 10.1038/s41598-017-17427-6.

    PMID: 29230013

    Molecules. 2017 Oct 27;22(11). pii: E1829.
    doi: 10.3390/molecules22111829.

    PMID: 29077044

    J Cell Biochem. 2018 Feb;119(2):2231-2239.
    doi: 10.1002/jcb.26385.

    PMID: 28857247

    Phytomedicine. 2018 Feb 1;40:37-47.
    doi: 10.1016/j.phymed.2017.12.030.

    PMID: 29496173
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.3852 mL 16.9262 mL 33.8524 mL 67.7048 mL 84.631 mL
    5 mM 0.677 mL 3.3852 mL 6.7705 mL 13.541 mL 16.9262 mL
    10 mM 0.3385 mL 1.6926 mL 3.3852 mL 6.7705 mL 8.4631 mL
    50 mM 0.0677 mL 0.3385 mL 0.677 mL 1.3541 mL 1.6926 mL
    100 mM 0.0339 mL 0.1693 mL 0.3385 mL 0.677 mL 0.8463 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.
    Argentinine References Information
    Citation [1]

    Nat Prod Res. 2004 Jun;18(3):265-8.

    A new dehydroaporphine alkaloid from Papaver fugax.[Pubmed: 15143838]
    A new dehydroaporphine alkaloid (-)-6a,7-dehydrofloripavidine has been isolated from the aerial parts of Papaver fugax Poir. (Papaveraceae) collected from Erzurum (Eastern Anatolia). (-)-Floripavidine (aporphine) and (-)-mecambrine (proaporphine) were isolated as major alkaloids. Other bases present were (+)-salutaridine (promorphinane) and Argentinine (phenanthrene). The presence of Argentinine has been shown for the first time in the Papaveraceae.
    Citation [2]

    Chem Pharm Bull (Tokyo). 2002 Dec;50(12):1613-5.

    Chromone and phenanthrene alkaloids from Dennettia tripetala.[Pubmed: 12499602]
    Dennettine, a new 2,6-dimethoxychromone and three known phenanthrene alkaloids (uvariopsine, stephenanthrine and Argentinine) in addition to the phenolic and known compound vanillin were isolated from the roots of Dennettia tripetala. Their structures were determined by physical and spectroscopical one dimensional (1D) and 2D-NMR analysis, including heteronuclear multiple bond correlation and nuclear Overhauser enhancement spectroscopy.
    Citation [3]

    J Nat Prod. 1994 Jul;57(7):890-5.

    New aporphine alkaloids from guatteria foliosa.[Pubmed: 7964785]
    Four new alkaloids were obtained from Guatteria foliosa, namely, the noraporphines (-)-3-methoxyputerine [1] and (+)-norguattevaline [2], the more highly oxidized (+)-3-methoxyguattescidine [3], and the oxoaporphine 3-methoxyoxoputerine [4]. Among several other known alkaloids also found in this same plant, (-)-3-hydroxynornuciferine, (-)-isoguattouregidine, and Argentinine exhibited significant activity against Trypanosoma cruzi.