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filingDate 1996-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa6386d5a98fe67e05e18c7a5dbae115
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c79d7802257fc9b71558e198287f285
publicationDate 1996-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9640740-A1
titleOfInvention Peptide and method of obtaining it
abstract The invention pertains to medicine, specifically to methods of obtaining biologically active substances with immunoregulatory properties, and can be used in medicine, veterinary science and experimental biochemistry. The problem addressed by the invention is that of producing a novel synthetic biologically active peptide with immunoregulatory properties of formula X-A-D-Trp-Y, in which A is D-Glu, iD-GLu; X is H or Gly, Ala, Leu, Ile, Val, Nval, Pro, Tyr, Phe, Trp, D-Ala, D-Leu, D-Ile, D-Val, D-NVal, D-Pro, D-Tyr, D-Phe, D-Trp, η-aminobutyric acid, κ-aminocaproic acid; Y is Gly, Ala, Leu, Ile, Val, Nval, Pro, Tyr, Phe, Trp, D-Ala, D-Leu, D-Ile, D-Val, D-NVal, D-Pro, D-Tyr, D-Phe, D-Trp, η-aminobutyric acid, κ-aminocaproic acid, -OH or substituted amide (C1-C3). The method of producing the peptide involves the synthesis of glutamil-containing peptides in solution by scission of an internal anhydride of tributyloxycarbonyl glutamic (D or L) acid with the appropriate k-salt of D-Trp-Y. This is followed by chromatographic separation of the α- and η isomers. Further synthesis was carried out by building up a peptide chain using activated esters of tributyloxycarbonylamino acids.
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priorityDate 1995-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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