Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bb75b0b19820e3833ebdcb31603b242b |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D505-00 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D505-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D505-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-535 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D505-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D505-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5365 |
filingDate |
1977-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate |
1980-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84b111fb5c1a05685d6146c4cef6e47f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_15833e9037e75c946510d2c69246aab4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9aac8a7e33596f82753e3a85a4cbbcde http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f52e8e2e5b087da5f5cd820a81d66094 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5396d9847ac39e91ab6a58c40935253 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d3bda0d9faf1be02fc93487b232158d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9425c06b3cd837bd368baa37125dda8 |
publicationDate |
1980-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
SU-786901-A3 |
titleOfInvention |
Method of preparing 7-substituted aminoacetamidooxadethiacephalosporins |
abstract |
Antibacterial 7-substituted aminoacetamido oxadethiacephalosporins of the formula: <IMAGE> [wherein R is substituted amino, substituted phenyl, or 5- or 6-membered hetero ring; Ar is aryl; Y is hydrogen or methoxy; Het is 5- or 6-membered aromatic hetero ring; and Z is hydroxy or carboxy protecting group] preparable e.g. by acylation of 7 alpha -methoxy-7 beta -amino-3-heterocyclic thiomethyl-3-cephem-4-carboxylic acid derivatives, are highly active against gram-positive and gram-negative bacteria, especially those resistant to other cephalosporins and penicillins. |
priorityDate |
1976-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |