http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S55153792-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D519-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-545
filingDate 1979-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_64bf4428d69a997e1caabf4a0f5289b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79482cdbb998e5892c120632db5cf851
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publicationDate 1980-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S55153792-A
titleOfInvention Cephalosporanic acid derivative
abstract NEW MATERIAL:The title compound of formula I [R<1> is H, formula II (R<3> is H or lower alkanoyl group); R<2> is lower alkanoyloxy group; etc.; -A- is -(CH2)n- CHR<6>-(R<6> is H, etc.; n is 1 or 2), or formula III]. EXAMPLE:7-[ 2-( 6,7-Dihydro-1-oxo-1H,5H-benzo[ ij ]quinolidine-2-carboxamido )- 2-phenylacetamido]-3-( acetyloxymethyl )-8-oxo-5-thia-1-azabicyclo[4,2,0]oct-2-ene- 2-carboxylic acid. USE:An antibacterial effective against Gram-positive and Gram-negative bacteria, with low toxicity, and capable of showing antibacterial actions on bacteria resistant to streptomycin. PROCESS:A compound of formula 10 (R<9> is lower alkyl group; X<2> is halogen) is reacted with a cephaloglycine of formula 11 to give the compound of formula I.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6525049-B2
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Total number of triples: 30.