http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SE-8406517-L
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4acae202b6a15394281949545e70d2f6 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-587 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-59 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-546 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-545 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-46 |
| filingDate | 1984-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26f707c480adc0c0d57119cb9c87a8f0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2c7f4893b4a4f6ec5b67c62063d87977 |
| publicationDate | 1984-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | SE-8406517-L |
| titleOfInvention | ALKYLOXIMS-SUBSTITUTED 7- (2-AMINO-4-THIAZOLYL) -ACETAMIDO-CEPHALOSPORANIC ACID DERIVATIVES, PREPARATION AND USE OF SUCH MEDICINAL PRODUCTS AND COMPOSITIONS CONTAINING THESE COMPOUNDS |
| abstract | Novel syn isomers of 7-(2-amino-4-thiazolyl)-acetamido-cephalosporanic acid compounds of the formula <IMAGE> I wherein R is selected from the group consisting of -(CH2)n-S-R2, -CHF2 and -(CH2)n-S-CN, R2 is selected from the group consisting of optionally protonated <IMAGE> n is an integer from 1 to 4, R1 is selected from the group consisting of hydrogen, chlorine, methoxy, alkyl and alkylthio of 1 to 5 carbon atoms, cycloalkyl of 3 to 5 carbon atoms, azidomethyl, acetoxymethyl, carbamoyloxymethyl, <IMAGE> and -CH2-S-R', Alk is alkyl of 1 to 4 carbon atoms, R' is selected from the group consisting of an optionally substituted nitrogen containing heterocycle and an acyl of an aliphatic acid of 2 to 4 carbon atoms, A is selected from the group consisting of hydrogen and an easily cleavable ester and when R is -(CH2)n-SR2, the COOA group may be the anion -COO-and when R is -(CH2)n-SCN or -CHF2, A may further be selected from the group consisting of an equivalent of an alkali metal, an alkaline earth metal, magnesium, -NH4 and a non-toxic, pharmaceutically acceptable organic amine and their non-toxic, pharmaceutically acceptable acid addition salts having antibiotic properties and a novel process and novel intermediates for their preparation. |
| priorityDate | 1979-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 31.