http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0028482-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ba090c867801ab7bccb082f1b694ad25 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-435 |
| filingDate | 1980-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67fd015f9ca7622cd4d4eaef75f41baf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b95556a608b527021e1d685e5d46deb |
| publicationDate | 1981-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0028482-A1 |
| titleOfInvention | Guanidine compounds, process for preparing them and compositions containing them |
| abstract | The invention provides compounds of formula (I):-n and pharmaceutically acceptable acid addition salts thereof, which are useful as histamine H 2 -antagonists. In formula (I) Z is sulphur or methylene and A is a covalent bond or methylene or ethane-1,2-diyl optionally substituted with one C 1-4 alkyl group and a second C 1-4 alkyl group or a phenyl C 1-4 alkyl group. n A particular compound of formula (I) is 2-[2- (2- guanidino-4-thiazolyl methylthio)ethylamino-]-3-nitro-1,4,5,6-tetrahydropyridine. |
| priorityDate | 1979-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 77.