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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d709e3167fa2f99a1803c9cfeb0aca63
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D498-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-08
filingDate 1981-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1981-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-2073737-A
titleOfInvention Rifamycins
abstract New rifamycin compounds of the formulae I and II <IMAGE> Y=H or CH3CO; R1 is C1-C7 alkyl or C3-C4 alkenyl, R2 is C1-C7 alkyl, C2-C4 chloroalkyl, C3-C4 alkenyl, Cycloalkyl having 3 to 7 C atoms in the ring, cycloalkyl alkyl having 3 to 6 C atoms in the ring, phenyl, bornyl, or C7-C8 aralkyl, unsubstituted or mono-substituted by a halogen atom in the aryl group; or NR1R2 is a cyclic moiety having 5 to 8 C atoms unsubstituted or substituted by 1 or 2 CH3 group(s), 4-alkyl-1-piperzinyl, morpholino or 1,2,3,4- tetrahydroisoquinolinyl, which inhibit the growth of gram positive bacteria and mycobacterium tuberculosis, are prepared by formation of the imino group.
priorityDate 1980-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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