PPAR


PPARs (peroxisome proliferator-activated receptors) are a group of nuclear receptor proteins that function as transcription factors regulating the expression of genes. PPARs play essential roles in the regulation of cellular differentiation, development, and metabolism (carbohydrate, lipid, protein), and tumorigenesis of higher organisms.
  • Rosiglitazone EY1422

    Rosiglitazone (罗格列酮; BRL-49653) 是PPARγ高亲和性激动剂。

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  • Pioglitazone HCl EY1405

    Pioglitazone hydrochloride (盐酸吡格列酮; U 72107A; AD 4833) 是PPARγ刺激剂。

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  • GW0742 EY1156

    GW0742是一种有效的,选择性PPARβ/δ激动剂,IC50为1 nM,比作用于hPPARα和hPPARγ选择性高1000倍。

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  • Pioglitazone EY0997

    Pioglitazone是一种选择性过氧化物酶体增殖物激活受体γ激动剂。

    More
  • T0070907 EY0423

    T0070907 (T007), a potent and selective PPARγ inhibitor, can reduce α and β tubulin proteins in some cancer cell lines. T0070907是一种选择性的PPARγ抑制剂,IC50为1 nM,比作用于PPARα和PPARδ选择性高800倍以上。

    More
  • Rosiglitazone EY1422

    Rosiglitazone (罗格列酮; BRL-49653) 是PPARγ高亲和性激动剂。

    More
  • Pioglitazone HCl EY1405

    Pioglitazone hydrochloride (盐酸吡格列酮; U 72107A; AD 4833) 是PPARγ刺激剂。

    More
  • GW0742 EY1156

    GW0742是一种有效的,选择性PPARβ/δ激动剂,IC50为1 nM,比作用于hPPARα和hPPARγ选择性高1000倍。

    More
  • Pioglitazone EY0997

    Pioglitazone是一种选择性过氧化物酶体增殖物激活受体γ激动剂。

    More
  • T0070907 EY0423

    T0070907 (T007), a potent and selective PPARγ inhibitor, can reduce α and β tubulin proteins in some cancer cell lines. T0070907是一种选择性的PPARγ抑制剂,IC50为1 nM,比作用于PPARα和PPARδ选择性高800倍以上。

    More
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