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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J71-001
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P33-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J5-0038
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J5-00
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filingDate 1977-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a21fa494840c63368f2d51986105f62a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3da95067f90e6a52dd209b488e8223a0
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publicationDate 1979-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2753839-A1
titleOfInvention NEW CORTICOIDS
abstract Corticoids of formula (I) are new (..... indicates a single or double bond; X is beta-hydroxymethylene or CO; R1 is H or physiologically tolerable acid residue. R2 is F, Cl or CH3). They are prepd. e.g. by hydroxylation of 11-unsubstd. cpds. e.g. by fermentation. (I) are antiinflammatories with minimal thymolytic catabolic or mineral-corticoid side effects. They are useful for treating e.b. eczema, polyarthritis, hay fever, respiratory allergies etc. Typical oral doses contain 0.1-50 mg. (I) and typical aerosols for inhalation 0.01-2% (I). In an example, 11beta,-21-dihydroxy-6,16alpha-dimethyl-4,6-pregnadiene-3,20-dion- e was prepd. from the 21-hydroxy by fermentation with Curvularia lunata NRRL 2380.
priorityDate 1977-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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