http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4324789-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D203-12
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D203-12
filingDate 1980-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1982-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46272f8fff9904defdef2781adfb365e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b47027c320dedcc996738089bfe5d53
publicationDate 1982-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4324789-A
titleOfInvention 1-Benzyl-5-nitro-4-(pyridyl or imidazolyl) alkylamino-1,2,3,6-tetrahydropyrimidines and blocking of histamine H2
abstract 2,3-Unsaturated nitrogen-containing heterocyclic compounds with a 3-nitro group and a 2-heterocyclyl alkylamino group. The alkyl group of 2-position substituents is preferably interrupted by sulfur or oxygen. The compounds of the invention are preferably dihydropyrroles or tetrahydropyrridines or pyrimidines. The compounds of the invention are histamine H2-receptor antagonists.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022034121-A1
priorityDate 1978-05-30-04:00^^<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: 476.