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AMI 1, protein arginine methyltransferase inhibitor (ab141472)

Key features and details

  • Potent, selective and reversible protein arginine methyltransferase inhibitor
  • CAS Number: 20324-87-2
  • Purity: > 97%
  • Soluble in water to 100 mM and in DMSO to 100 mM
  • Form / State: Solid
  • Source: Synthetic

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Overview

  • Product name

    AMI 1, protein arginine methyltransferase inhibitor
  • Description

    Potent, selective and reversible protein arginine methyltransferase inhibitor
  • Biological description

    Potent, selective and reversible protein arginine methyltransferase inhibitor (IC50 = 1.63 μM). ROS° scavenger with antioxidant effects (IC50 = 8.3 μM). Inhibits arginine in vitro without competing for the AdoMet binding site. Modulates nuclear receptor-regulated transcription in vivo. Cell-permeable.

  • Purity

    > 97%
  • CAS Number

    20324-87-2
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    7,7'-(Carbonyldiimino)bis[4-hydroxy2-naphthalenesulfonic acid] disodium salt
  • Molecular weight

    548.45
  • Molecular formula

    C21H14N2Na2O9S2
  • PubChem identifier

    88489
  • Storage instructions

    Store at -20°C. It is important to note that this product is reported to be light sensitive. Store In the Dark. Store under desiccating conditions.
  • Solubility overview

    Soluble in water to 100 mM and in DMSO 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

    C1=CC2=C(C=C(C=C2C=C1NC(=O)NC3=CC4=CC(=CC(=C4C=C3)O)S(=O)(=O)[O-])S(=O)(=O)[O-])O.[Na+].[Na+]
  • Source

    Synthetic

  • Research areas

    • Cell Biology
    • Cell Cycle
    • Cell Cycle Inhibitors
    • p53
    • Cell Biology
    • Apoptosis
    • Intracellular
    • p53 Pathway
    • Epigenetics and Nuclear Signaling
    • Chromatin Modifying Enzymes
    • Methylation
    • Epigenetics and Nuclear Signaling
    • Chromatin Modifying Enzymes
    • Acetylation
    • Microbiology
    • Interspecies Interaction
    • Host Virus Interaction
    • Tags & Cell Markers
    • Subcellular Markers
    • Nucleus
    • Other Nuclear Bodies
    • Epigenetics and Nuclear Signaling
    • Nuclear Signaling Pathways
    • Nuclear Receptors
    • Co-activators/co-repressors
    • Epigenetics and Nuclear Signaling
    • Cell cycle
    • Cell Cycle Inhibitors
    • p53
    • Epigenetics and Nuclear Signaling
    • Transcription
    • Co-factors
    • Epigenetics and Nuclear Signaling
    • Chromatin Modifying Enzymes
    • Methylation
    • Arginine Methylation
    • Epigenetics and Nuclear Signaling
    • Chromatin Modifying Enzymes
    • Acetylation
    • HDACs
    • Class III / Sir2 class
    • Cancer
    • Cell cycle
    • Cell cycle inhibitors
    • p53 pathway
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    • Product Range
    • Just Add Water
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    • Biochemicals
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    • Signaling
    • Epigenetics
    • Histone Acetyltransferases (HATs)
    • Biochemicals
    • Pharmacology
    • Signaling
    • Epigenetics
    • Histone Methyltransferase (HMT)
    • Biochemicals
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    • Transferase
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    • Biochemicals
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    • Cancer
    • Epigenetics
    • Histone Acetyltransferases (HATs)
    • Biochemicals
    • Research Area
    • Cancer
    • Epigenetics
    • Histone Methyltransferase
    • Biochemicals
    • Research Area
    • Epigenetics
    • Histone Acetyltransferases (HATs)
    • Biochemicals
    • Research Area
    • Epigenetics
    • Histone Methyltransferase
    • Biochemicals
    • Pharmacology
    • Enzymes
    • Transferase
    • Histone Methyltransferase (HMT)
    • Protein arginine methyltransferase (PRMT)

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