http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0863148-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5d5bb9b9a6d998b72b154ceb1895a3f5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ec7aa9366c4867ba95ac5cd4fbbaec25
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-16
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-16
filingDate 1997-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c9be1c640073944203bbab38c7f4256
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bbe1edf13b84d15fa659be8cb9e668fd
publicationDate 1998-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0863148-A1
titleOfInvention Compounds derived from adenosine, use of such compound as a medicament, method for synthesizing such a compound and intermediates thereof
abstract The invention relates to compounds derivednfrom adenosine and analogs thereof, to the use of suchncompounds in pharmaceutical compositions as a cardiotonic,na renal protectant, a cognition enhancer and/ornan antiasthmatic, to a method and to intermediates fornsynthesizing such a compound. n The compounds according to the inventionnhave the general formula (I):n n wherein R 1 is a straight or branched alkyl,ncycloalkyl, aralkyl or aryl group or H; R 2 is a straight or branched alkyl, cycloalkyl,naralkyl, aryl group each of which is optionally substitutednby at least one C 1-4 alkyl, C 1-4 alkoxy, nitro group ornhalogen; R 3 is CH 2 R 4 or CONHR 5 ; R 4 is H, OH, OR 5 , SR 5 ; R 5 is H, an alkyl or a cycloalkyl group; or a pharmaceutically acceptable salt thereof.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2020509997-A
priorityDate 1997-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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