p53 Inhibitors: Products

p53 is well known for its key role as a tumor suppressor protein. It is 393 amino acids (aa) in length with a predicted molecular weight of 44 kDa. It belongs to the p53 family that also includes p63 and p73. Structurally, p53 is characterized by an N-terminal transactivation domain, central DNA-binding and oligomerization domains, and a C-terminal regulatory domain. It is thought to exist as a homotetramer, and it exhibits approximately 72% and 76% aa identity with its mouse and rat orthologs, respectively. Mutations in the p53 gene are one of the most frequent genomic events accompanying oncogenic transformation. p53 responds to signals such as DNA damage or cell stress primarily through its actions as a transcription factor. Among its gene targets are a range factors that promote DNA repair mechanisms or apoptosis including cell cycle regulatory proteins and members the Bcl-2 family. Because of its critical role in genomic homeostasis, p53 activities are tightly regulated by a network of protein-protein interactions, microRNAs, and a range of post-translational modifications, including phosphorylation, acetylation, methylation, and ubiquitination. A widely studied regulator is Murine Double Minute 2 (MDM2). MDM2 is known to suppress p53 activity through direct binding or through its actions as a Ubiquitin ligase (E3) that catalyzes p53 ubiquitination and proteasome-mediated degradation.

Showing 1-9 out of 9 p53 Inhibitors Products

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Pifithrin-α hydrobromide


p53 inhibitor. Also aryl hydrocarbon receptor agonist
12672  
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Pifithrin-μ


Inhibitor of p53-mitochondrial binding
26534  
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Nutlin-3


MDM2 antagonist; inhibits MDM2-p53 interaction
39841  
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Cyclic Pifithrin-α hydrobromide


p53 inhibitor
3843 
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HLI 373


Hdm2 inhibitor; activates p53-dependent transcription
3503 
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SJ 172550


MDMX inhibitor. Disrupts MDMX-p53 interaction
3929 
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RITA


MDM2-p53 interaction inhibitor
24431  
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NSC 66811


MDM2 antagonist. Disrupts MDM2-p53 interaction
2936 
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SP 141


High affinity MDM2 inhibitor
5332 
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