http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01199977-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
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filingDate 1988-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0663b2f8fd1c88d1361881732b7e434e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c3195b01859566ac2d9114b7f7e39900
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publicationDate 1989-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01199977-A
titleOfInvention Crystal of cephalosporin derivative, production thereof and drug composition comprising said crystal as active ingredient
abstract NEW MATERIAL:Crystal of (6R,7R)-7-[ 2-( 2-amino-4-thiazolyl )-2-[ Z-[( 2- carboxy-4,5-dihydroxyp henyl )methyl ]oxyimino ]acetamido ]-3-[ (2-carboxy-5- methyl-S-triazol o[ 1,5-a ]pyrimidin-7-yl )thiomethyl ]-8-oxo-5-thia-1-azabicyclo[ 4,2,0 ]oct-2-enecarboxylic acid shown by the formula and a nontoxic salt thereof in a solvent form. n EXAMPLE: Crystal of a compound shown by formula-formic acid solvate. n USE: An active component for a drug composition. Being characterized by specific infrared absorption spectrum or specific diffraction pattern of powder X-ray crystal diffraction, having no absorbing properties, stable even in long-term preservation and useful for infectious diseases. n PREPARATION: A compound shown by the formula or a nontoxic salt thereof is dissolved in a solvent such as water or formic acid at -40W80°C and crystal is precipitated to give crystal of the compound shown by the formula. n COPYRIGHT: (C)1989,JPO&Japio
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priorityDate 1987-11-16-04:00^^<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: 33.