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    CAS No. 51-67-2 Price $50 / 20mg
    Catalog No.CFN96470Purity>=98%
    Molecular Weight137.18Type of CompoundAlkaloids
    FormulaC8H11NOPhysical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)
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    Featured Products
    Mulberroside F

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    Arteannuin B

    Catalog No: CFN98807
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    Tyramine Description
    Source: The herbs of Uncaria rhynchophylla
    Biological Activity or Inhibitors: 1. Tyramine is a major mutagen precursor in soy sauce, being convertible to a mutagen by nitrite.
    2. Tyramine is a genuine neurotransmitter in other invertebrates and possibly in vertebrates as well.
    3. Tyramine is the biological precursor of octopamine, both compounds are independent neurotransmitters, acting through various G-protein coupled receptors, they are antagonistic modulators of behavior and metabolism.
    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.
    Recent ChemFaces New Products and Compounds
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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.

    PMID: 29496173
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 7.2897 mL 36.4485 mL 72.8969 mL 145.7938 mL 182.2423 mL
    5 mM 1.4579 mL 7.2897 mL 14.5794 mL 29.1588 mL 36.4485 mL
    10 mM 0.729 mL 3.6448 mL 7.2897 mL 14.5794 mL 18.2242 mL
    50 mM 0.1458 mL 0.729 mL 1.4579 mL 2.9159 mL 3.6448 mL
    100 mM 0.0729 mL 0.3645 mL 0.729 mL 1.4579 mL 1.8224 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.
    Tyramine References Information
    Citation [1]

    Neuron, 2005 ,46 (2) :247-60.

    Tyramine Functions independently of octopamine in the Caenorhabditis elegans nervous system.[Reference: WebLink]
    Octopamine biosynthesis requires tyrosine decarboxylase to convert tyrosine into Tyramine and Tyramine beta-hydroxylase to convert Tyramine into octopamine. We identified and characterized a Caenorhabditis elegans tyrosine decarboxylase gene, tdc-1, and a Tyramine beta-hydroxylase gene, tbh-1. The TBH-1 protein is expressed in a subset of TDC-1-expressing cells, indicating that C. elegans has Tyraminergic cells that are distinct from its octopaminergic cells. tdc-1 mutants have behavioral defects not shared by tbh-1 mutants. We show that Tyramine plays a specific role in the inhibition of egg laying, the modulation of reversal behavior, and the suppression of head oscillations in response to anterior touch. We propose a model for the neural circuit that coordinates locomotion and head oscillations in response to anterior touch. Our findings establish Tyramine as a neurotransmitter in C. elegans, and we suggest that Tyramine is a genuine neurotransmitter in other invertebrates and possibly in vertebrates as well.
    Citation [2]

    Arch Insect Biochem Physiol. 2003 Sep;54(1):1-13.

    Tyramine and octopamine: antagonistic modulators of behavior and metabolism.[Pubmed: 12942511 ]
    The phenolamines Tyramine and octopamine are decarboxylation products of the amino acid tyrosine. Although Tyramine is the biological precursor of octopamine, both compounds are independent neurotransmitters, acting through various G-protein coupled receptors. Especially, octopamine modulates a plethora of behaviors, peripheral and sense organs. Both compounds are believed to be homologues of their vertebrate counterparts adrenaline and noradrenaline. They modulate behaviors and organs in a coordinated way, which allows the insects to respond to external stimuli with a fine tuned adequate response. As these two phenolamines are the only biogenic amines whose physiological significance is restricted to invertebrates, the attention of pharmacologists was focused on the corresponding receptors, which are still believed to represent promising targets for new insecticides. Recent progress made on all levels of octopamine/Tyramine research enabled us to better understand the molecular events underlying the control of complex behaviors.
    Citation [3]

    Gan. 1984 Jan;75(1):1-3.

    Tyramine is a major mutagen precursor in soy sauce, being convertible to a mutagen by nitrite.[Pubmed: 6373470]
    Tyramine was identified as a new mutagen precursor in Japanese soy sauce, becoming mutagenic after treatment with nitrite under acidic conditions. The mutagenic compound was identified as 4-(2-aminoethyl)-6-diazo-2,4- cyclohexadienone , and its specific mutagenic activity was 112 revertants/micrograms towards Salmonella typhimurium TA100 without S9 mix.