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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D499-48
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-48
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filingDate 1976-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f9afab28820555d2fb9052628b62d0a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9f3941c3afbb65e35a3482f78defa74
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publicationDate 1977-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2626418-A1
titleOfInvention LACTAMANTIBIOTICS AND THE PROCESS FOR THEIR MANUFACTURING
abstract Beta-Lactam derivs. of formula (I) are new. In (I) n = 1-4, Z = C(CH3)2 or -CH2.C(A)=R = H, opt. substd. alkyl, phthalide residue or a cation. A = H, alkoxy, halo or CH2Y. Y = H, acyloxy, alkoxy, opt. substd. pyridinium, opt. substd. carbamoyl (in which the substits. may complete a ring) or SR1. R1 = acyl, alkyl, or an opt. substd. 5 or 6 membered heterocycle which may be fused to a 5 or 6 membered aromatic ring. (I) are antibiotics effective against Gram positive and negative bacteria including penicillinase-producing Staphylococci. They are administered in usual oral or pref. parenteral formulations. In an example, 7-(3,3,3-trifluoropropionylamino)cephalosporanic acid was prepd. from 7-ACA and 3,3,3-trifluoropropionyl chloride.
priorityDate 1976-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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