http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010273848-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a94cc448c9840e65d6cbe922b79f68c6
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-46
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4166
filingDate 2008-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55550b8719e1dde49bd331da7a121dca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_737f29ab4d898a6e3d3c8278f83c34d9
publicationDate 2010-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2010273848-A1
titleOfInvention Iminopyrrolidone thiol amino acid conjugates, pharmaceutical compositions and methods for the treatment of cancer
abstract Compounds, compositions and methods for the treatment of cancer are disclosed herein. Embodiments of the present invention include compounds having the formula: (I), wherein R1 is selected from hydrogen or substituted or unsubstituted (C 1 -C 6 ) alkyl or (C 3 -C 6 ) cycloalkyl, R 2 and R 3 are independently selected from hydrogen, substituted or unsubstituted (C 1 -C 6 ) alkyl, (C 4 -C 6 ) cycloalkyl, or taken together with the N atom to which they are attached form a 3-6 membered heterocycloalkyl, and n is 1-5. Embodiments of the present invention also include pharmaceutical compositions comprising compounds of Formula (I) or pharmaceutically acceptable salts thereof, and methods of treating cancer via the administration of such compounds to patients in need of such treatment.
priorityDate 2007-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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