http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5728080-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_97ddd4d1d0ebc8a7d2c8e7d214d08cf3
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-58
filingDate 1980-07-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f1a8b8b787b3a5460e0cf7f21dd9d62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d8501a389511627d2d75270c8c5cd70e
publicationDate 1982-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5728080-A
titleOfInvention Novel chromene type compound
abstract NEW MATERIAL:A compound shown by the formula (R 1 is H or lower alkyl; R 2 is H or lower aliphatic acyl group). n EXAMPLE: 2, 7-Dimethyl-2- ( 4,8-dimethylnona-3, 7-dienyl ) -5-hydroxy-2H-1-benzopyran-6-carboxylic acid (dauri chromenic acid). n USE: An antibacterial agent against Gram-positive bacteria, and a relaxing agent for smooth muscle. n PROCESS: The leaves of Rhododendron dauric um Linn., an ericaceous plant, for example, are soaked in methanol for two weeks to carry out methanol extraction. Methanol is removed from the methanol extracted solution, the residue is fractionated by silica gel column, and a fraction having antibacterial activity is fractioned by silica gel thin layer. The fraction having activity is fractionated again by silica gel column and purified, to give a compound shown by the formula. n COPYRIGHT: (C)1982,JPO&Japio
priorityDate 1980-07-25-04:00^^<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: 21.