http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2481285-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
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filingDate 1981-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6f252a438a9ffc1a03d9579c4ff03c5
publicationDate 1981-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2481285-A1
titleOfInvention NOVEL PYRAZOLO (1,2-A) (1,2,4) BENZOTRIAZINES, IN PARTICULAR USEFUL AS ANTI-INFLAMMATORY AGENTS, AND PROCESS FOR THE PREPARATION THEREOF
abstract THE INVENTION CONCERNS NEW PYRAZOLO1,2-A-1,2,4BENZOTRIAZINES USEFUL AS ANTI-INFLAMMATORY AND THEIR PREPARATION. THE MEDICINAL PRODUCTS OF THE INVENTION CONTAIN AS ACTIVE COMPOUND AN EFFECTIVE QUANTITY OF AT LEAST ONE COMPOUND OF GENERAL FORMULA (CF DRAWING IN BOPI) IN WHICH R IS A HYDROGEN ATOM OR A LOWER ALKYL GROUP, NITRO, AMINO, (LOWER ALKYLOERIEUR) AMINO , DI (LOWER ALKYL) AMINO, -SR, -OR OR A HALOGEN; R IS HYDROGEN, OR A LOWER ALKYL OR ARYLALKYL GROUP; R IS HYDROGEN, A LOWER ALKYL GROUP OR A SALIFIING ION; R IS HYDROGEN OR A LOWER ALKYL AND Y IS OXYGEN OR SULFUR. APPLICATIONS: ORAL OR PARENTERAL ADMINISTRATION IN UNIT DOSES OF APPROXIMATELY 10 TO 250 MG OF AN ACTIVE COMPOUND, OR LOTIONS, OINTMENTS OR CREAMS CONTAINING ABOUT 0.1 TO 3 OF THE ACTIVE COMPOUND.
priorityDate 1980-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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