http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S57102194-A

Outgoing Links

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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-91
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P17-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-04
filingDate 1980-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e31d4a1c95a3940ec0c29baef2cabe32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f6bcddeec65c12bf82f7db200a6fffe3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6531d43d37527c3f80971d8ea7955453
publicationDate 1982-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S57102194-A
titleOfInvention Preparation of cephalotaxine and ester thereof
abstract PURPOSE: To prepare the titled substance in a short time, by cultivating cells of a plant belonging to the genus Cephalotaxus, producing and accumulating the titled substance in the culture, and collecting the titled substance. n CONSTITUTION: A stem, leaf, root or other tissual slices or cellular groups of a plant belonging to the genus Cephalotaxus of the family Cephalotaxaceae, e.g. Cephalotaxus harringtonia or Cephalotaxus drupaceae Sieb. et Zucc. var. koraiana Makino, are sterilized, and then cultivated in the Murashige and Skoog culture medium to induce calluses. The resultant calluses are then cultivated on a solid culture medium or in a liquid culture medium by the same method as in the ordinary cultivation of microorganisms to multiply the aimed substance expressed by the formula. The aimed substance is separated by freeze-drying the cultivated cells, adding 95% ethanol thereto, and extracting the aimed substance at 30W35°C. n COPYRIGHT: (C)1982,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002507615-A
priorityDate 1980-12-17-04:00^^<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: 22.