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Merck
CN

Pilot screening programme for small molecule activators of p53.

International journal of cancer (2005-02-25)
Rachel G Berkson, Jonathan J Hollick, Nicholas J Westwood, Julie A Woods, David P Lane, Sonia Lain
摘要

Activation of the p53 tumour suppressor is predicted to have therapeutically beneficial effects. Many current anti-cancer therapies activate the p53 response via DNA damage. Non-genotoxic activation of the p53 pathway would open the way to long-term and possibly prophylactic treatments. We have established a simple protocol to screen small compound libraries for activators of p53-dependent transcription, and to select and characterise the most interesting hits, which include non-genotoxic activators. These compounds or their derivatives are of potential clinical interest. This approach may also lead to the identification of novel p53-activating compound families and possibly to the description of novel molecular pathways regulating p53 activity.

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Sigma-Aldrich
MDMX Inhibitor, NSC207895, The MDMX Inhibitor, NSC207895 controls the biological activity of MDMX. This small molecule/inhibitor is primarily used for Cancer applications.