Literature DB >> 20100001

Patented inhibitors of p53-Mdm2 interaction (2006 - 2008).

Lutz Weber1.   

Abstract

IMPORTANCE OF THE FIELD: Induction of apoptosis by reactivation of p53 in cancer cells is an emerging therapeutic concept for the treatment of cancer. The discovery and design of novel small molecules that block the p53-Mdm2 protein interaction, thereby activating p53, has provided interesting drug candidates that have currently entered clinical trials or are at the preclinical development stage. AREAS COVERED IN THIS REVIEW: A selection of the interesting patents focusing on small molecule inhibitors of the p53-Mdm2 interaction, recorded from 2006 until 2009, is presented together with a review of the related structural chemistry space. WHAT THE READER WILL GAIN: Readers will rapidly gain an overview of the majority of patented scaffolds of small molecule inhibitors of the p53-Mdm2 protein-protein interaction and learn about current limitations and properties of these compounds. TAKE HOME MESSAGE: The discovery p53-Mdm2 protein-protein interaction inhibitors have delivered new potential options for a targeted cancer therapy with drug-like, non-toxic small molecules. If successful, this approach could gain considerably more attention in the pharmaceutical industry by targeting a variety of validated intracellular protein-protein interactions.

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Year:  2010        PMID: 20100001     DOI: 10.1517/13543770903514129

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  12 in total

1.  miR-605 joins p53 network to form a p53:miR-605:Mdm2 positive feedback loop in response to stress.

Authors:  Jiening Xiao; Huixian Lin; Xiaobin Luo; Xiaoyan Luo; Zhiguo Wang
Journal:  EMBO J       Date:  2011-01-07       Impact factor: 11.598

Review 2.  The structure-based design of Mdm2/Mdmx-p53 inhibitors gets serious.

Authors:  Grzegorz M Popowicz; Alexander Dömling; Tad A Holak
Journal:  Angew Chem Int Ed Engl       Date:  2011-02-21       Impact factor: 15.336

3.  Senotherapeutic drugs for human intervertebral disc degeneration and low back pain.

Authors:  Hosni Cherif; Daniel G Bisson; Matthew Mannarino; Oded Rabau; Jean A Ouellet; Lisbet Haglund
Journal:  Elife       Date:  2020-08-21       Impact factor: 8.140

4.  Identification of FDA-approved drugs that computationally bind to MDM2.

Authors:  Wayne A Warner; Ricardo Sanchez; Alex Dawoodian; Esther Li; Jamil Momand
Journal:  Chem Biol Drug Des       Date:  2012-07-23       Impact factor: 2.817

5.  The p53-MDM2/MDMX axis - A chemotype perspective.

Authors:  Kareem Khoury; Grzegorz M Popowicz; Tad A Holak; Alexander Dömling
Journal:  Medchemcomm       Date:  2011       Impact factor: 3.597

Review 6.  Targeting p53-MDM2-MDMX loop for cancer therapy.

Authors:  Qi Zhang; Shelya X Zeng; Hua Lu
Journal:  Subcell Biochem       Date:  2014

7.  Swimming into peptidomimetic chemical space using pepMMsMIMIC.

Authors:  Matteo Floris; Joel Masciocchi; Marco Fanton; Stefano Moro
Journal:  Nucleic Acids Res       Date:  2011-05-27       Impact factor: 16.971

8.  MDM2 SNP309 promoter polymorphism and p53 mutations in urinary bladder carcinoma stage T1.

Authors:  Hans Olsson; Per Hultman; Johan Rosell; Peter Söderkvist; Staffan Jahnson
Journal:  BMC Urol       Date:  2013-01-28       Impact factor: 2.264

9.  Overexpression of the catalytically impaired Taspase1 T234V or Taspase1 D233A variants does not have a dominant negative effect in T(4;11) leukemia cells.

Authors:  Carolin Bier; Rouven Hecht; Lena Kunst; Sabine Scheiding; Désirée Wünsch; Dorothée Goesswein; Günter Schneider; Oliver H Krämer; Shirley K Knauer; Roland H Stauber
Journal:  PLoS One       Date:  2012-05-03       Impact factor: 3.240

Review 10.  Chemical Variations on the p53 Reactivation Theme.

Authors:  Carlos J A Ribeiro; Cecília M P Rodrigues; Rui Moreira; Maria M M Santos
Journal:  Pharmaceuticals (Basel)       Date:  2016-05-13
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