http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007143507-A3

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7333a9700d96ba02d498fa22f82b9067
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H17-08
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-70
filingDate 2007-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63ee96544bef199f2f52359f48c56a04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49ea74e430e32f76e36d6a4bace277ad
publicationDate 2008-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2007143507-A3
titleOfInvention Preparation and utility of substituted erythromycin analogs
abstract The present disclosure is directed to novel macrolide antibiotics of Formula (I) and pharmaceutically acceptable salts and prodrugs thereof; and the chemical syntheses and medical uses of these novel macrolide antibiotics for the treatment and/or management of infections caused by various aerobic and anaerobic gram-positive and gram-negative microorganisms as well as various mycobacteria.
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priorityDate 2006-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 405.