http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0108627-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C17-208
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-545
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-546
filingDate 1983-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f761552d82127dc86658061aacf85138
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_770d304b5831152a6c1ff030b194bec3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d388648d430138376da43c0d70a230c1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9925541794ffa84711b9ccfdaa03a954
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8a16a0908da029bfb78c4345fd1ff424
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8e96bb7177c75c0cbebe34b33a2e4c6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63bec1a020f2d19734999dd51421f677
publicationDate 1984-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0108627-A2
titleOfInvention Cephalosporin derivatives and process for producing the same
abstract A compound of the general formula:n wherein A represents an unsubstituted thiazolyl or substituted thiazolyl residue having at least one substituent which is halogen, alkyl, amino or acylamido; R' represents hydrogen or alkyl, carboxymethyl or alkoxycarbonylmethyl, R 2 represents hydrogen or methyl, hydroxymethyl, acyloxymethyl or alkylthiomethyl, or represents thiadiazolylthiomethyl optionally alkyl substituted, or represents tetrazolylthiomethyl residue optionally substituted by alkyl, alkylaminoalkyl or carboxymethyl; and R 3 represents unsubstituted allyl or substituted allyl having at least one substituent which is halogen, alkyl, cycloalkyl, haloalkyl, acyloxy alkyl, alkoxycarbonyl, phenyl or substituted phenyl, or salts thereof have excellent chemical stability and are very satisfactorily absorbed to exhibit an excellent therapeutic effect on the patients having bacterial infectious diseases when administered by a method other than injection, such as oral administration. Various methods are disclosed for the preparation and formulation of the new compounds.
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priorityDate 1982-11-05-04:00^^<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: 737.