http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5441885-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_91ce16ac3dbceb38cb5e6983c8c15a5a
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7042
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7048
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H17-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-70
filingDate 1977-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1272f5d374f12f366f0ab168dc9f131b
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publicationDate 1979-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5441885-A
titleOfInvention Antibiotic of 3-deacyloxy-sixteen-membered macrolide
abstract NEW MATERIAL:Compounds of formulaI(R 1 is lower alkanoyl; A is vinylene, ethylene, B is 1, 3-butadienylene, tetramethylene) and their salts. n EXAMPLE: 3-Deacetoxy-2, 3-didehydroleucomycin A 3 . n USE: Antibiotics. It has an antibiotic spectra against grampositive and negative bacteria similar to conventional macrolide antibiotics. Further it has no bitter taste and it can be orally dosed especially useful as syrup for infants. n PREPARATION: A conventional biotic such as leucomycin A 3 or gosamycin, of formula II (R 2 is acetyl, propionyl) is subjected to deacyloxylation on the 3-position in a hydrophilic organic solvent to afford said compound of formula III. n COPYRIGHT: (C)1979,JPO&Japio
priorityDate 1977-09-02-04:00^^<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: 23.