p53

p53 (TP53) is a transcription factor whose protein levels and post-translational modification state alter in response to cellular stress (e.g. hypoxia, DNA and spindle damage). Activation of p53 occurs by several mechanisms including phosphorylation by ATM, ATR, Chk1 and MAPKs.

Products for p53

  1. Cat.No. Product Name Information/Activity
  2. BCC2241 Pifithrin-α (PFTα) Pifithrin-α hydrobromide is a p53 inhibitor which blocks its transcriptional activity and prevents cells from apoptosis. Pifithrin-α hydrobromide is also an aryl hydrocarbon receptor (AhR) agonist. Pifithrin-α (PFTα) chemical structure
  3. BCC2407 Cyclic Pifithrin-α hydrobromide Pifithrin-β hydrobromide (PFT β hydrobromide) is a potent p53 inhibitor with an IC50 of 23 μM. Cyclic Pifithrin-α hydrobromide chemical structure
  4. BCC2412 Pifithrin-μ Pifithrin-μ is an inhibitor of p53 and HSP70, with antitumor and neuroprotective activity. Pifithrin-μ chemical structure
  5. BCC2408 HLI 373 Hdm2 inhibitor; activates p53-dependent transcription HLI 373 chemical structure
  6. BCC2410 NSC 146109 hydrochloride NSC 146109 hydrochloride is a small-molecule p53 activator that target MDMX and could be of value in treating breast cancer. NSC 146109 hydrochloride is a pseudourea derivative, promotes breast cancer cells to undergo apoptosis through activating p53 and inducing expression of proapoptotic genes[1]. NSC 146109 hydrochloride chemical structure
  7. BCC2242 NSC 319726 NSC319726 (ZMC1) is a mutant p53R175 reactivator; inhibits growth of fibroblasts expressing the p53R175 mutation (IC50 = 8 nM); shows no inhibition for p53 wild-type cells. NSC 319726 chemical structure
  8. BCC2255 NSC 66811 MDM2 inhibitor. Disrupts MDM2-p53 interaction NSC 66811 chemical structure
  9. BCC2238 RITA (NSC 652287) RITA is an inhibitor of p53-HDM-2 interaction, binds to p53dN, with a Kd of 1.5 nM, and also induces DNA-DNA cross-links. RITA (NSC 652287) chemical structure
  10. BCC2416 SJ 172550 SJ-172550 is a small molecule inhibitor of MDMX; competes for the wild type p53 peptide binding to MDMX with an EC50 of 5 μM. SJ 172550 chemical structure
  11. BCC2239 Tenovin-1 Tenovin-1 is an inhibitor of sirtuin 1 and sirtuin 2, an activator of p53 and may have potential in the management of cancer. Tenovin-1 chemical structure

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