CAY10681

CAY10681

CAT N°: 15573
Price:

From 109.00 92.65

Inactivation of the tumor suppressor p53 commonly coincides with increased signaling through NF-?B in cancer. CAY10681 is a dual modulator of p53-MDM2 interaction and NF-?B signaling.{25314} It potently binds MDM2 (Ki = 250 nM), reducing MDM2-mediated turnover of p53.{25314} CAY10681 also inhibits phosphorylation of I?B? and dose-dependently reduces nuclear accumulation of p65.{25314} It blocks the proliferation of cancer cell lines (IC50s range from 33 to 37 µM).{25314} CAY10681 exhibits excellent oral bioavailability and inhibits tumor growth in A549 xenografts in nude mice.{25314}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • 4-(4-bromophenyl)-4,5-dihydro-5-[3-(1H-imidazol-1-yl)propyl]-3-phenyl-1-(phenylmethyl)-pyrrolo[3,4-c]pyrazol-6(1H)-one
  • Correlated keywords
    • biochemical inhibitor cancer intracellular signaling gene regulation inflammation NF-?B dual modulator p53-MDM2 interaction bind mediated turnover inhibit phosphorylation I?B? reduce reduction nuclear accumulation p65 block proliferation cell line oral bioavailability bioavailable tumor growth A549 xenograft in vivo vitro
  • Product Overview:
    Inactivation of the tumor suppressor p53 commonly coincides with increased signaling through NF-?B in cancer. CAY10681 is a dual modulator of p53-MDM2 interaction and NF-?B signaling.{25314} It potently binds MDM2 (Ki = 250 nM), reducing MDM2-mediated turnover of p53.{25314} CAY10681 also inhibits phosphorylation of I?B? and dose-dependently reduces nuclear accumulation of p65.{25314} It blocks the proliferation of cancer cell lines (IC50s range from 33 to 37 µM).{25314} CAY10681 exhibits excellent oral bioavailability and inhibits tumor growth in A549 xenografts in nude mice.{25314}

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