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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-62
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-28
filingDate 1988-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf18e6fae7fbf9e6ca6198ca0cf53ef2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81ce59525e29c1d44a40c412c9788b8a
publicationDate 1991-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-202555-B
titleOfInvention Process for producing peptid-alcohol derivatives of anticoagulant activity
abstract Human proinsulin in crystalline form which comprises a salt of a complex of human proinsulin and divalent zinc ion, the cation of said salt being selected from the group consisting of lithium, calcium, sodium, potassium, ammonium, magnesium, and barium. The preparation comprisesn (a) preparing an aqueous mixture containing from about 5 to about 50 mg/ml human proinsulin, from about 0.1 to about 5 mg/ml of a phenolic substance, from about 0.03 to about 0.6 milliequivalents/ml of a salt of a cation selected from the group consisting of lithium, calcium, sodium, potassium, ammonium, magnesium, and barium, and from about 0.2 to about 5 milliequivalents of Zn⁺² cation; (b) adjusting the aqueous mixture to a pH in the range of from about 5.4 to about 6.5; (c) allowing crystal formation to occur; and (d) recovering crystalline human proinsulin from the aqueous mixture.
priorityDate 1987-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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