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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D309-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-351
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-35
filingDate 1980-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1982-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_40d8ee487f2c76a1529b274ec6687b77
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_db75be5b1873223860704adf142f2b8c
publicationDate 1982-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4312867-A
titleOfInvention Antibacterial compounds, processes for their preparation and compositions containing them
abstract Compounds of formula (II): <IMAGE> (II) <IMAGE> +TR <IMAGE> Z represents a divalent radical derived from a C1-20 alkane, C3-8 cycloalkane, C2-20 alkene, arene, aralkane, cycloalkylalkane, heterocycle, or heterocylylalkane; and Rx and Ry are the same or different and each represent (a) hydrogen, or (b) C1-20 alkyl, C2-8 alkenyl, either of which may be optionally substituted with C3-7 cycloalkyl, halogen, carboxy, C1-6 alkoxycarbonyl, carbamyl, aryl, heterocyclyl, hydroxy, C1-6 alkanoyloxy, amino, mono- or di-(C1-6) alkylamino; or (c) C3-7 cycloalkyl optionally substituted with C1-6 alkyl; or (d) aryl; or (e) heterocyclyl; or (f) Rx and Ry together with the nitrogen atom to which they are attached represent a C5-7 heterocyclic ring, are useful as antibacterial and antimycoplasma agents.
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priorityDate 1979-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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