http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2011124602-A1

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filingDate 2007-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a7f5d556d6707e3c05c79fa55db01bb
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publicationDate 2011-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2011124602-A1
titleOfInvention Stat3 Inhibitor Having Anti-Cancer Activity and Methods
abstract A small-molecule Stat3 dimerization inhibitor, S3I-M2001, is described and the dynamics of intracellular processing of activated Stat3 within the context of the biochemical and biological effects of the Stat3 chemical probe inhibitor are elucidated. S3I-M2001 is a newly-identified oxazole-based peptidomimetic of the Stat3 Src Homology (SH) 2 domain-binding phosphotyrosine peptide that selectively disrupts active Stat3:Stat3 dimers. Stat3-dependent malignant transformation, survival, and migration and invasion of mouse and human cancer cells harboring persistently-activated Stat3 were inhibited by S3I-M2001. S3I-M2001 inhibited Stat3-dependent transcriptional regulation of tumor survival genes, such as Bcl-xL. The disclosed compound is useful as a new potential treatment for certain cancers.
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