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Biochemicals

Apocynin, NADPH-oxidase inhibitor (ab120615)

Price and availability

30 153 ₸

Availability

Order now and get it on Thursday February 25, 2021

Apocynin, NADPH-oxidase inhibitor (ab120615)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Selective NADPH-oxidase inhibitor
  • CAS Number: 498-02-2
  • Purity: > 99%
  • Soluble in DMSO to 100 mM and in ethanol to 100 mM
  • Form / State: Solid
  • Source: Synthetic

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Overview

  • Product name

    Apocynin, NADPH-oxidase inhibitor
  • Description

    Selective NADPH-oxidase inhibitor
  • Biological description

    Selective NADPH-oxidase inhibitor (IC50 = 10 μM). Inhibits production of reactive oxygen species. Also elicits a range of in vitro and in vivo anti-inflammatory effects.

  • Purity

    > 99%
  • CAS Number

    498-02-2
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    4'-Hydroxy-3'-methoxyacetophenone
  • Molecular weight

    166.18
  • Molecular formula

    C9H10O3
  • PubChem identifier

    2214
  • Storage instructions

    Store at Room Temperature. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in DMSO to 100 mM and in ethanol to 100 mM
  • Handling

    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 -20°C. Generally, these will be useable for up to one month. 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 visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    CC(=O)C1=CC(=C(C=C1)O)OC
  • Source

    Synthetic

  • Research areas

    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Pharmacology
    • Enzymes
    • Oxidases
    • NADPH oxidase
    • Inhibitors
    • Metabolism
    • Pathways and Processes
    • Redox metabolism
    • Oxidative stress
    • Biochemicals
    • Pharmacology
    • Signaling
    • Signal transduction
    • Nitric oxide & oxidative stress
    • ROS
    • Biochemicals
    • Research Area
    • Cancer
    • Signal transduction
    • Nitric oxide & oxidative stress
    • ROS
    • Biochemicals
    • Pharmacology
    • Signaling
    • Immunomodulators
    • Immunomodulators & Immunosuppressants

Images

  • Functional Studies - Apocynin, NADPH-oxidase inhibitor (ab120615)
    Functional Studies - Apocynin, NADPH-oxidase inhibitor (ab120615)
    ab19534 staining glutathione in A549 cells treated with apocynin (ab120615), by ICC/IF. Increase in glutathione expression correlates with increased concentration of apocynin, as described in literature.
    The cells were incubated at 37°C for 24h in media containing different concentrations of ab120615 (apocynin) in DMSO, fixed with 4% formaldehyde for 10 minutes at room temperature and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with ab19534 (10 µg/ml) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight 488 goat anti-mouse polyclonal antibody (ab96879) at 1/250 dilution was used as the secondary antibody.
  • Functional Studies - Apocynin, NADPH-oxidase inhibitor (ab120615)
    Functional Studies - Apocynin, NADPH-oxidase inhibitor (ab120615) Image from Wang T et al., PloS one., 9(3): e91063. Fig 6.; doi: 10.1371/journal.pone.0091063 Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/

    A–B. Endothelial cells were transfected with Nef cDNA, incubated for further 6 hours and treated with apocynin (200 nM), trolox (200 nM), Nox2 inhibitor (1 uM) or IKKi (100 nM). After additional 18 hours supernatants were analyzed for Nef-induced MCP-1 production (A) and endothelial cells for apoptosis using TUNEL (B). C–D. Endothelial cells were cocultured with Nef-transfected Jurkat cells for 24 h, and then treated with apocynin (200 nM), trolox (200 nM), Nox2 inhibitor (1 uM) or IKKi (100 nM) and incubated an additional 18 h, then analyzed for Nef-induced MCP-1 production (C) and apoptosis of endothelial cells (D). Data were expressed as fold MCP-1 production and apoptosis, normalized to the mean of control measurements. Data represent mean±SD from 3 separate experiments in which measurements were made in triplicate. *P

    Wang T et al., PloS one., 9(3): e91063. Fig 6.; doi: 10.1371/journal.pone.0091063

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