http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2702911-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-14
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-36
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filingDate 1977-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75f33554e9eb94e0b60d6badd636eb73
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7d31296d4ab95cff2c5c2062e030baf
publicationDate 1978-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2702911-A1
titleOfInvention NEW PHENYL ACID DERIVATIVES
abstract Phenylacetic acid derivs. of formula (I) are new. In the formula, n is 1-3; R1 is halogen, CF3, NO2 or amino; R2 and R3 are each H or lower alkyl, or together are ethylene; X1 is H2 or O; and Y1 is CN, CONHOH, CONH2, 5-tetrazolyl or COOH (I) are opt. in the form of a salt, ester or amide with a physiologically acceptable base, alcohol or amine). (I) are pharmacologically active cpds. or intermediates for these. They are esp. used as systemic antiinflammatory agents with good gastric compatibility and resorbability low toxicity-rapid onset of action and high and lasting activity. They can be used for treating polyarthritis, neurodermites, bronchial asthma, hay fever etc. Dose is e.g. 1-250 mg orally.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0007319-A1
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priorityDate 1977-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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