http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BG-51621-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2d8c925859b6134256f29b8bc52a46a5 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-64 |
filingDate | 1992-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81d2aaf6e103b6fdcdff0d574bc2665d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_afed9162e401ffb34eb8f35f2690d5b1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_78912a07b023a233b74be691efed682d |
publicationDate | 1993-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | BG-51621-A1 |
titleOfInvention | Penicillin analogues and method for their preparation |
abstract | The compounds belong to the penicillin group and may be applied as active substances in the composition of medications with antibacterial effect. They are prepared following a simplified technology and have the following general formula:<IMAGE>where Pyr is pyrrole residue with the following structure:<IMAGE>where, if R is H, R1 is COOCH3 and when R is CH3, R1 is CH3CO or COOC2H5. They are prepared through acylation of the amino group of 6-aminopenicillanic acid with mixed anhydride, obtained from the respective pyrrolic acid and alkylchloroformiate. |
priorityDate | 1992-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 19.