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BzATP triethylammonium salt

BzATP, Benzoylbenzoyl-ATP, 2′(3′)-O-(4-Benzoylbenzoyl)adenosine 5′-triphosphate triethylammonium salt
An Agonist of P2X7 Receptors
Cat #: A-385
Alternative Name BzATP, Benzoylbenzoyl-ATP, 2′(3′)-O-(4-Benzoylbenzoyl)adenosine 5′-triphosphate triethylammonium salt
  • Lyophilized Powder
  • Bioassay Tested
    • Source Synthetic
    MW: 1018.97
    Purity: >95%
    Effective concentration 0.5-300 µM.
    Chemical name [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy(phosphonooxy)phosphoryl]oxyphosphoryl]oxymethyl]oxolan-3-yl] 4-benzoylbenzoate;N,N-diethylethanamine.
    Molecular formula C24H24N5O15P3 · C18H45N3.
    CAS No.: 112898-15-4.
    PubChem CID 71308559
    Activity BzATP triethylammonium salt is an agonist of the purinergic P2X7 receptor, more potent than ATP, with EC50 varying from 0.7 to 285 µM, depending on receptor species, buffer composition, serum constituents and repeated exposure to ATP. Shows partial agonist activity on other P2 receptors. Can be used as a photoaffinity label for ATPase1-3.
    Shipping and storage Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C.
    Solubility Soluble up to 100 mM in water. Centrifuge all products before handling (10000 x g 5 min).
    Storage of solutions -20°C. It is recommended to aliquot stock solutions to prevent repeated thawing and freezing.
      • Alomone Labs BzATP triethylammonium salt activates human P2X7 receptors expressed in HEK-293 cells.
        Dose response curve of hP2X7 activation by BzATP triethylammonium salt (#A-385). Cells were loaded with Fluo-8 NW dye, and stimulated with increasing concentrations of BzATP triethylammonium salt. Changes in intracellular Ca2+ following agonist application were detected as changes in maximum relative fluorescence (RLU) using FLIPRTETRA™.

      • BzATP triethylammonium salt is an agonist of the purinergic P2X7 receptor that is ten times more potent than ATP1. On rat P2X7 receptor, BzATP triethylammonium salt demonstrates an EC50 value of 6.8 µM2. The compound also shows partial agonist activity on other P2X receptors1.

        P2X receptors are a family of ion channels gated by ATP, a ligand that mediates numerous physiological functions. P2X receptors are widely localized in cell types of almost every origin, including neuronal, muscular, epithelial and immune and have been shown to play a pivotal role in models of various pain conditions2.
    Target P2X7 receptors
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    Last update: 18/07/2019

    BzATP triethylammonium salt (#A-385), is a highly pure, synthetic, and biologically active compound.

    For research purposes only, not for human use
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