http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004517819-A

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Predicate Object
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H17-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H17-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7048
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
filingDate 2001-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2004-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2004517819-A
titleOfInvention Ketolide antibacterial agent
abstract The present invention provides a compound of the formula: wherein X is hydrogen or a halogen group; R 2 is hydrogen, acyl, or a hydroxy protecting group; R 6 is hydrogen, hydroxyl, or —OR a [wherein , Ra are C 1 -C 10 alkyl, C 2 -C 10 alkenyl, C 2 -C 10 alkynyl, aryl, heterocyclo, aryl (C 1 -C 10 ) alkyl, aryl (C 2 -C 10 ) alkenyl, A substituted or unsubstituted moiety selected from the group consisting of aryl (C 2 -C 10 ) alkynyl, heterocyclo (C 1 -C 10 ) alkyl, heterocyclo (C 2 -C 10 ) alkenyl and heterocyclo (C 2 -C 10 ) alkynyl R 13 is hydrogen, or a moiety is methyl; C 3 -C 10 alkyl, C 2 -C 10 alkenyl, C 2 -C 10 alkynyl, aryl, heterocyclo, aryl (C 1 -C 10 ) alkyl, aryl (C 2 -C 10 ) alkenyl, aryl (C 2 -C 10 ) alkynyl, heterocyclo (C 1 -C 10 ) alkyl, heterocyclo R is hydrogen or a moiety that is C 1 -C 10 alkyl, C 1 -C 10 alkyl, C 2 -C 10 alkenyl and a substituted or unsubstituted moiety selected from the group consisting of heterocyclo (C 2 -C 10 ) alkynyl; 2 -C 10 alkenyl, C 2 -C 10 alkynyl, aryl, heterocyclo, aryl (C 1 -C 10) alkyl, aryl (C 2 -C 10) alkenyl, aryl (C 2 -C 10) alkynyl, heterocyclo (C 1 -C 10) alkyl, heterocyclo (C 2 -C 10) alkenyl And a substituted or unsubstituted moiety selected from the group consisting of heterocyclo (C 2 -C 10 ) alkynyl and pharmaceutically acceptable salts, esters and prodrug forms thereof. These compounds have anti-infective activity and are useful for the treatment of bacterial and protozoal infections.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008508322-A
priorityDate 2000-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 392.