http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0532671-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-04
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filingDate 1991-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07bd4530acb69b22b3379104b16723e9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_875408d26b1c9832c37741a5ead49696
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publicationDate 1993-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0532671-A
titleOfInvention Novel cem compound, its production method and antibacterial agent
abstract (57) [Summary] (Modified) [Purpose] Development of new cephalosporin derivatives with excellent antibacterial activity. A novel cephem compound represented by the following formula and a pharmacologically acceptable salt or physiologically hydrolyzable non-toxic ester thereof. [In the formula, R 1 is an optionally substituted lower alkyl group, A trityl group; R 2 is a hydrogen atom, a metal atom, a protecting group for a carboxyl group, etc .; R 3 , R 4 , R 5 and R 6 are hydrogen atoms, halogen atoms, lower alkyl groups, etc .; R 7 is a hydrogen atom , Halogen atom, CN or COOR 8 (R 8 is a hydrogen atom or a lower alkyl group); R 9 is an amino group which may be protected; Z is N or CH; and n is 0 or 1. [Effect] This compound has a strong antibacterial activity against Gram-positive bacteria and Gram-negative bacteria, and also has a wide range of balanced antibacterial activities up to Staphylococcus aureus and Pseudomonas aeruginosa which are resistant to all antibacterial agents. .
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9967256-A1
priorityDate 1990-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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