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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-60
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filingDate 1987-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ffa7c58b6723278ee201cf4e3e7c7e1
publicationDate 1989-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6416775-A
titleOfInvention Sesterterpenoids
abstract NEW MATERIAL:The sesterterpenoids of formula [R is (substituted)furyl or 2-oxo-5-hydroxy-2,5-dihydrofuryl]. EXAMPLE:20-beta-Furyl-16-sodium sulfinoxy-(E)-13,18-dehydro-18(S)-methylcleistan. USE:A medicine having aldose reductase inhibiting action and useful e.g. as a remedy for neuropathy, retinopathy, cataract, etc., caused by diabetes. PREPARATION:Collected sponge is immediately frozen with liquid nitrogen or liquid air and crushed with a crusher or homogenizer, etc., at <=-150 deg.C. The obtained fine powder is freeze-dried and extracted with an organic solvent. The objective compound is obtained by concentrating the extract and fractionating by adsorption chromatography, etc.
priorityDate 1987-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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