http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S54106491-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_39ae96c0ecc22ff90ff986371a3cea0f
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D505-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6561
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D205-085
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D205-08
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/C07D277-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-397
filingDate 1978-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b16fba1c4295e9f6c464abd7c29efdfb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_829898a2dbe7e55e24482f1ab9885e63
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1b260029e752d6d58caa9cea646b4d6c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a686dbd019bcf6f4e4bac587cf75678
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18b7290303bf3b99f4a7a5d1ac52093f
publicationDate 1979-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S54106491-A
titleOfInvention Cephalosporin analog or its salt, their preparation, and prophylactics and remedies for microbisms consisting mainly of them
abstract NEW MATERIAL:A compound of formula Ia: (R 1a is an aralkanoyl, aryloxyalkanoyl group which may be substituted, etc.; R 2 is COOH or protected COOH; Y is H or lower alkoxy group) and of formula II: (R 1 is NH 2 or substituted NH 2 ; R is hydroxymethyl, formly group, etc.; R' is H; R" is OH, halogen, etc; or may form a group =0, etc. together with R') and its salt. n EXAMPLE: 7 β-(2-Methoxyimino-2-phenyl-acetamido)-1-oxadethia-3-cephem-4-carboxylic acid (syn-isomer). n USE: Antibacterials, and intermediates for their synthesis, effective against Gram- positive and Gram-megative bacteria. n PROCESS: A compound of formula II, which is obtained from a compound of formula III: (X is halogen; R 6 is lower alkyl group) via several steps, is subjected to ring closure or oxidation to give a compound of formula IV, which is acylated, if necessary, to afford the compound of formula Ia. n COPYRIGHT: (C)1979,JPO&Japio
priorityDate 1977-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397482

Total number of triples: 25.