http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EA-023360-B1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-715
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-48
filingDate 2013-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7af7e4908b106a4a741d0ca2605f4a9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af93e04d5c059f01e23aa4e606454fe3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d583a3a5daff65c6057c6e9ccc6bb31a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51ecac778461fe29aebf6af86ece73fc
publicationDate 2016-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EA-023360-B1
titleOfInvention LINEAR ACYLASIDE PEGYLING AGENT, METHOD FOR ITS OBTAINING AND METHOD FOR OBTAINING PEGYLED INTERFERON
abstract The invention relates to the pharmaceutical industry, in particular to a pegylating agent capable of joining free amino groups of proteins to form an amide bond through an azide condensation reaction, as well as a method for producing it and a method for tahilating biologically active proteins, for example, interferons. The invention provides methods for producing a linear acyl azide pegylating agent and corresponding methods for pegylating interferons (IFN), in particular IFN α-2b. The technical result of the invention is a pegylating agent - a derivative of PEG-phenylalanine, capable of joining free amino groups of proteins with the formation of an amide bond through azide condensation without causing racemization of the substrate, which can be easily identified in the UV region from the aromatic fragment and quantified.
priorityDate 2013-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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