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filingDate 2001-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49ecc0ec1b568ddafab71599c73a4f8e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f46e94879610f097e895cd55d18fc5bf
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_74ab1459ad460f725a2f21a4782f1049
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_524da2d17b19c020d6cf03823d872a34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a784d8abcc86f94056e779e52f74d50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c86d0c2b55667368e03405c27c5fbff6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4185267e7ee6256bc89eb9b4487d7226
publicationDate 2003-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1353672-A2
titleOfInvention Synthesis of 3-amino-thalidomide and its enantiomers
abstract The invention provides new and useful analogs of 4-amino-thalidomide. These analogs include S(−)-4-amino-thalidomide and R(+)-4-amino-thalidomide. The invention also provides processes for making these analogs. Further, the invention provides methods for inhibiting angiogenesis and treating angiogenesis-associated diseases, including cancer and macular degeneration, by administering these compounds.
priorityDate 2000-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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