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filingDate 1991-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8038469391b9a585b8255f6835545bd9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_308598092074ce0ac1a892dc9ee9cc8d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_45f36019efba41494840c128e423c288
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a62dffc9d0c2f47bea0ad6182d96c61
publicationDate 1993-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0543568-A
titleOfInvention Tetronic acid derivative, production method and use thereof
abstract (57) [Summary] (Modified) [Purpose] To find a novel substance having phospholipase A 2 inhibitory activity, which is useful as an anti-inflammatory agent. [Structure] General formula [Chemical formula 1] [In the formula, R 1 represents hydrogen, a halogen atom, an acyl group having 2 to 25 carbon atoms which may have a substituent, or an alkyl group which may have a substituent, and R 2 represents a hydrogen or an alkyl group. , An aralkyl group or an acyl group having 2 to 25 carbon atoms, and R 3 represents an optionally substituted hydroxyl group or a halogen atom. ] A method for producing a compound represented by the following, or a salt thereof, and a microorganism belonging to the genus Streptomyces and capable of producing the above-mentioned tetronic acid derivative are cultured, and the compound is collected from the culture. [Effect] The compound of the present invention has low toxicity and is an inflammatory disease, It can be expected to be used for treatment or prevention of allergic diseases, thrombotic diseases, arteriosclerosis and the like.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6060600-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5977169-A
priorityDate 1990-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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