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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-91
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
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filingDate 1987-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de2e61de6fd98374d109abde7eab31b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb7ffd133db56882bdf0f3dedb785b9c
publicationDate 1989-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6455183-A
titleOfInvention Production of antitumor active substance
abstract PURPOSE:To mass-produce a vascular endothelial cell growth inhibitory factor with hardly any side effects, by cultivating a cellular strain derived from human chondrosarcoma in a specific culture medium. CONSTITUTION:Tissues collected from human chondrosarcoma are treated with trypsin to separate human chondrosarcoma-derived cellular strain (HCS) and provide individual cells, which are then inoculated into an MEM culture medium containing 20% FCS, etc., and subcultured at 37 deg.C while exchanging the culture medium every 2-4 days to afford the aimed HCS cells capable of exhibiting stable growth. 1-2X10<7> resultant cells are subsequently seeded onto a 800cm<2> plate and cultivated in Dulbecco's MEM culture medium containing 10% FCS added thereto for 3-4 weeks and then in serum-free Dulbecco's MEM culture medium for 48hr to recover the obtained culture fluid and provide a cultivation supernatant sample, which is subsequently dissolved in an aqueous solution of a salt, such as guanidine, at pH5-7. The obtained solution is then subjected to fractionation treatment with a membrane to afford the aimed vascular endothelial cell growth inhibitory factor contained in a fraction having >=10,000 molecular weight.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H04226274-A
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