http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2651395-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c24684033fba97d1ad845ce453a57e3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-20
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-545
filingDate 1976-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b6b0342b63c0ef0bcfe11652429e9a10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6337eb964d3ef723d277c3cea4f77487
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9f3941c3afbb65e35a3482f78defa74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f9afab28820555d2fb9052628b62d0a
publicationDate 1978-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2651395-A1
titleOfInvention CEPHEMDER DERIVATIVES AND PROCESS FOR THEIR PRODUCTION
abstract Cephalosporins of formula (I): (where n = 0 or 1, R1-3 are H or 1-5C alkyl but not 4-5C alkyl when n = 1, R4 is H, opt. substd. alkyl, phthalidyl or a cation, R5 is H or 1-3C alkyl A is H, alkoxy, halogen, or CH2Y, Y is H, acyloxy, alkoxy, opt. substd. pyridinium, opt. substd. carbamoyloxy or SR6, R6 is acyl, alkyl or an opt. substd. 5- or 6-membered heterocycle opt. fused with a 5- or 6-membered aromatic ring) are novel. Cpds. (I) are antibiotics active against Gram-positive and -negative bacteria, including penicillinase-producing Staphylococci. A typical cpd. is 7-(3-butenylamino)-cephalosporanic acid. In an example, this is prepd. from 3-butenoic acid and 7-aminocephalosporanic acid.
priorityDate 1976-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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