http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2003078248-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-66
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-381
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-66
filingDate 2002-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_846d139d3c18fe78ce7159d78454c4e3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1387ffc082a7a8d1b3c11bb4593efa6d
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publicationDate 2003-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2003078248-A1
titleOfInvention 2-amino-3-aroyl-4,5 alkylthiophenes: agonist allosteric enhancers at human A1 adenosine receptors
abstract The present invention relates to a compound of formula (I): n n n wherein: n R 3 is selected from the group consisting of 1-napthyl, 2-napthyl and cycloalkylphenyl; and n R 4 and R 5 taken together form a ring having from 5 to 10 carbon atoms. n Additionally, the invention provides a therapeutic method for preventing or treating a pathological condition or symptom in a mammal subject, such as a human, wherein increased angiogenesis is desired, comprising administering to a mammal in need of such therapy an effective amount of the aforementioned thiophene selective adenosine A 1 allosteric enhancer.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2003212082-A1
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priorityDate 2001-05-18-04:00^^<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: 417.