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GW 9662, PPARgamma antagonist (ab141125)

  • Datasheet
  • SDS
  • COA
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Chemical Structure - GW 9662, PPARgamma antagonist (ab141125)

    Key features and details

    • Selective PPARγ antagonist
    • CAS Number: 22978-25-2
    • Purity: > 99%
    • Soluble in ethanol to 50 mM
    • Form / State: Solid
    • Source: Synthetic

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    Overview

    • Product name

      GW 9662, PPARgamma antagonist
    • Description

      Selective PPARγ antagonist
    • Biological description

      Selective PPARγ antagonist (IC50 values are 3.3, 32, >1000 nM for PPARγ, PPARα and PPARδ respectively). Apoptotic and antimetastatic activity in vitro.

    • Purity

      > 99%
    • CAS Number

      22978-25-2
    • Chemical structure

      Chemical Structure

    Properties

    • Chemical name

      2-Chloro-5-nitro-N-phenylbenzamide
    • Molecular weight

      276.68
    • Molecular formula

      C13H9ClN2O3
    • PubChem identifier

      644213
    • Storage instructions

      Store at +4°C. The product can be stored for up to 12 months.
    • Solubility overview

      Soluble in ethanol to 50 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.

      Refer to SDS for further information

      Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

    • SMILES

      O=C(Nc1ccccc1)c2cc(ccc2Cl)[N+]([O-])=O
    • Source

      Synthetic

    • Research areas

      • Cardiovascular
      • Lipids / Lipoproteins
      • Lipid Metabolism
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      • Transcription
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      • Neural Signal Transduction
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      • Transcription
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      • Epigenetics and Nuclear Signaling
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      • Estrogen
      • Epigenetics and Nuclear Signaling
      • Nuclear Signaling Pathways
      • Nuclear Receptors
      • Retinoic & Retinoid
      • Epigenetics and Nuclear Signaling
      • Nuclear Signaling Pathways
      • Nuclear Receptors
      • Testosterone
      • Epigenetics and Nuclear Signaling
      • Transcription
      • Other factors
      • Epigenetics and Nuclear Signaling
      • Transcription
      • Transcription Factors
      • Epigenetics and Nuclear Signaling
      • Nuclear Signaling Pathways
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      • Orphan Nuclear Receptors
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      • PPAR
      • Metabolism
      • Pathways and Processes
      • Mitochondrial Metabolism
      • Mitochondrial Biogenesis
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      • Pathways and Processes
      • Metabolic signaling pathways
      • Nucleotide metabolism
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    Images

    • Chemical Structure - GW 9662, PPARgamma antagonist (ab141125)
      Chemical Structure - GW 9662, PPARgamma antagonist (ab141125)
      2D chemical structure image of ab141125, GW 9662, PPARgamma antagonist

    Protocols

    To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

    Click here to view the general protocols

    Datasheets and documents

    • SDS download

    • Datasheet download

      Download
    • COA

    References (8)

    Publishing research using ab141125? Please let us know so that we can cite the reference in this datasheet.

    ab141125 has been referenced in 8 publications.

    • Huang W  et al. Sildenafil protects against pulmonary hypertension induced by hypoxia in neonatal rats via activation of PPAR?-mediated downregulation of TRPC. Int J Mol Med 49:N/A (2022). PubMed: 34935055
    • Shoaito H  et al. The Role of Peroxisome Proliferator–Activated Receptor Gamma (PPAR?) in Mono(2-ethylhexyl) Phthalate (MEHP)-Mediated Cytotrophoblast Differentiation. Environ Health Perspect 127:27003 (2019). PubMed: 30810372
    • Liu L  et al. Hydroxysafflor-Yellow A Induces Human Gastric Carcinoma BGC-823 Cell Apoptosis by Activating Peroxisome Proliferator-Activated Receptor Gamma (PPAR?). Med Sci Monit 24:803-811 (2018). PubMed: 29417935
    • García C  et al. Benefits of VCE-003.2, a cannabigerol quinone derivative, against inflammation-driven neuronal deterioration in experimental Parkinson's disease: possible involvement of different binding sites at the PPAR? receptor. J Neuroinflammation 15:19 (2018). PubMed: 29338785
    • Degrelle SA  et al. New Transcriptional Reporters to Quantify and Monitor PPAR?Activity. PPAR Res 2017:6139107 (2017). PubMed: 29225614
    • Zhu HY  et al. Peroxisome proliferator-activated receptor-? agonist troglitazone suppresses transforming growth factor-ß1 signalling through miR-92b upregulation-inhibited Axl expression in human keloid fibroblasts in vitro. Am J Transl Res 8:3460-70 (2016). PubMed: 27648136
    • Jin X  et al. Pioglitazone alleviates inflammation in diabetic mice fed a high-fat diet via inhibiting advanced glycation end-product-induced classical macrophage activation. FEBS J 283:2295-308 (2016). PubMed: 27062545
    • Zhu HY  et al. Peroxisome proliferator-activated receptor-? agonist inhibits collagen synthesis in human keloid fibroblasts by suppression of early growth response-1 expression through upregulation of miR-543 expression. Am J Cancer Res 6:1358-70 (2016). PubMed: 27429849

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