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fxr antagonist dy268  (MedChemExpress)


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    MedChemExpress fxr antagonist dy268
    Fxr Antagonist Dy268, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fxr+antagonist+dy268/pm41819510-68-0-8?v=MedChemExpress
    Average 94 stars, based on 1 article reviews
    fxr antagonist dy268 - by Bioz Stars, 2026-08
    94/100 stars

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    94
    MedChemExpress fxr antagonist dy268
    Fxr Antagonist Dy268, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fxr+antagonist+dy268/pm41819510-68-0-8?v=MedChemExpress
    Average 94 stars, based on 1 article reviews
    fxr antagonist dy268 - by Bioz Stars, 2026-08
    94/100 stars
      Buy from Supplier

    90
    Axon Medchem LLC dy268 (fxr antagonist)
    Effect of seladelpar on the FXR pathway in primary mouse hepatocytes. Primary mouse hepatocytes were treated with either seladelpar (10 μM) or the FXR agonist GW4064 (10 μM) in combination with either DMSO or the FXR antagonist <t>DY268</t> (10 μM) for 48 h, and gene expression analysis was performed. Data are presented as mean ± S.E.M. of at least three independent replicates. ∗ p < 0.05 and ∗∗ p < 0.01 denote the significant difference between control and seladelpar or GW4064 in each condition. FXR, Farnesoid X receptor.
    Dy268 (Fxr Antagonist), supplied by Axon Medchem LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fxr+antagonist+dy268/pmc09214809-132-0-5?v=Axon+Medchem+LLC
    Average 90 stars, based on 1 article reviews
    dy268 (fxr antagonist) - by Bioz Stars, 2026-08
    90/100 stars
      Buy from Supplier

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    Effect of seladelpar on the FXR pathway in primary mouse hepatocytes. Primary mouse hepatocytes were treated with either seladelpar (10 μM) or the FXR agonist GW4064 (10 μM) in combination with either DMSO or the FXR antagonist DY268 (10 μM) for 48 h, and gene expression analysis was performed. Data are presented as mean ± S.E.M. of at least three independent replicates. ∗ p < 0.05 and ∗∗ p < 0.01 denote the significant difference between control and seladelpar or GW4064 in each condition. FXR, Farnesoid X receptor.

    Journal: The Journal of Biological Chemistry

    Article Title: Selective PPARδ agonist seladelpar suppresses bile acid synthesis by reducing hepatocyte CYP7A1 via the fibroblast growth factor 21 signaling pathway

    doi: 10.1016/j.jbc.2022.102056

    Figure Lengend Snippet: Effect of seladelpar on the FXR pathway in primary mouse hepatocytes. Primary mouse hepatocytes were treated with either seladelpar (10 μM) or the FXR agonist GW4064 (10 μM) in combination with either DMSO or the FXR antagonist DY268 (10 μM) for 48 h, and gene expression analysis was performed. Data are presented as mean ± S.E.M. of at least three independent replicates. ∗ p < 0.05 and ∗∗ p < 0.01 denote the significant difference between control and seladelpar or GW4064 in each condition. FXR, Farnesoid X receptor.

    Article Snippet: DY268 (FXR antagonist) was from Axon Medchem.

    Techniques: Gene Expression, Control