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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D301-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-33
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H15-20
filingDate 2005-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2006-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100658002-B1
titleOfInvention Isolation and Purification of Matyr Resinol and Actigenin from Forsythia Fruits
abstract The present invention relates to a method for isolating and purifying matyresinol and actinigen from forsythia fruit, and inactive lignans present in the ducts by treating the degreasing methanol extract of ducts with a mixed enzyme containing pectinase and cellulase. The glycosides of matyrethinosides and actin were converted to the active aglycone component matyrethinol and actigenin, followed by diion HP-20 ion resin or silica gel column chromatography, and finally Sephadex LH-20 column chromatography. It is effective in effectively separating and purifying matairesinol and actigenin. Therefore, the separation and purification method of the present invention can not only mass produce phytohormone-like components of matyrethinol and actigenin from ducts, but also widely use these components as cancer, heart disease and osteoporosis therapeutics and cosmetic new materials for skin aging. Can be used.n n n n Forsythia, Pectinase, Cellulase, Diaion HP-20 Ion Resin, Silica Gel, Sephadex LH-20 Column Chromatography, Matyr Resinol, Actigenin
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103432207-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101438332-B1
priorityDate 2005-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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