http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103665044-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1e059b4e2268ae09ba48bfce7f3b9b86
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6561
filingDate 2013-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e47a3697b0aa2f753afe8bceb5198163
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3e0aaa376832dae0e237d54cd947d0bd
publicationDate 2015-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103665044-B
titleOfInvention Adefovir dipivoxil compound
abstract The invention relates to the field of pharmacy and in particular relates to an adefovir dipivoxil compound. Adefovir dipivoxil is a crystal; an X-ray powder diffraction pattern measured through Cu-Ka is represented by the figure 10. The purity of the adefovir dipivoxil compound disclosed by the invention can be up to 99.95-99.9 percent. According a crystallization method disclosed by the invention, the solvent content is low, and the adefovir dipivoxil compound is safe and reliable in clinical application. A stability test shows that the adefovir dipivoxil crystal compound disclosed by the invention is high in stability, and a preparation of the adefovir dipivoxil crystal compound is high in dissolution rate.
priorityDate 2013-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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