http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100540021-B1

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H17-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-7048
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-351
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-351
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7048
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H17-08
filingDate 2001-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2005-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100540021-B1
titleOfInvention Erythromycin derivative having novel crystal structures and processes for their production
abstract The present invention relates to N-demethyl-N-isopropyl-12-methoxy-11-oxo-anhydroerythromycin having a strong diffraction peak at diffraction angles (2θ) of 5.6 ° and 10.4 ° by powder X-ray diffraction. E form crystals of A-6,9-halfacetal fumaric acid salts, E form crystals prepared by treating C form crystals of fumaric acid salts of the compounds at 20 ° C. to 40 ° C. in a mixed solvent consisting of ethyl acetate and water, and E form crystals Provides Form D crystals that are made via light oil. The crystal contains little residual solvent and is suitable for pharmaceutical preparation.
priorityDate 2000-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5959088-A
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8857
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425258636

Total number of triples: 24.