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filingDate 1997-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a7b21e02c7326eecd4a4946ab168a4e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46f35d87f883ebc59b0e9f45802a64c5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_27e9cdfec7f2260790a00b0799413afa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5716ba1c91f496a57ffd11d864e0ffb6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51dcb4bf9b7fce1cb999d60751721972
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77284231353f8f86d3b325604c3db15d
publicationDate 2003-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SK-283467-B6
titleOfInvention Quinoxalinediones, process and intermediates for their manufacture, their use and pharmaceutical compositions based thereon
abstract The quinoxalinediones of formula (I) wherein R is a 5-membered heteroaryl containing 3 or 4 N heteroatoms attached to the quinoxalinedione ring via a C or N ring, or a 6-membered heteroaryl containing 1 to 3 N heteroatoms, which is attached to the quinoxalinedione ring via ring C, each of which optionally has a fused benzo group and each of these groups, including the fused benzo group, is optionally substituted with 1 or 2 substituents; R 1 and R 2 are each independently H, F, Cl, Br, alkyl of 1 to 4 C or haloalkyl of 1 to 4 C; and pharmaceutically acceptable salts thereof; a process and intermediates for making these quinoxalinedions; pharmaceutical compositions based on these compounds and their use. à
priorityDate 1996-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 388.