http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2330037-C1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_535e7dbf801667176c11df53f97f039d
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-22
filingDate 2006-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_45f656635c2b3b1c3db44ab38995eaf0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eac220dab086963a8fd114326bfd60c7
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publicationDate 2008-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2330037-C1
titleOfInvention METHOD OF CHLORINE e6 PRODUCTION
abstract FIELD: medicine; pharmacology. n SUBSTANCE: invention refers to pharmacology, namely to production of biologically active compounds, specifically to improved method of chlorine e6 production applied for production of photosensitisers for photodynamic cancer therapy. Method is performed by processing sulphuric acid concentrated spirulina methanolic suspensions followed by filtration, dilution with water, alkali neutralisation by, filtration of settled deposition through celite layer followed with washing in hot water and petroleum-ether, elution with acetone celite, silica gel based chromatography, recrystallisation of mixed chloride methylene- methanol, release of produced alkylpheophorbide and its dilution with acetone, alkali processing, hydrochloric acid neutralisation, a filtration through celite layer, washing in water, aqueous ammonia, lyophilisation, dilution with aqueous alkali, filtration through sephadex layer, neutralisation, centrifugation and lyophilisation. n EFFECT: production of pure product with reagents taken in small amounts. n 1 cl, 6 ex
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2646477-C1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2568597-C1
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priorityDate 2006-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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