http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-201333032-A

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filingDate 2012-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49ec6de748025fd72e1cb2fd472959d1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9cf7b5b0364e549d1ad20c3b152f5108
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publicationDate 2013-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-201333032-A
titleOfInvention Site-specific GLP-2 conjugate using immunoglobulin fragments
abstract The present invention relates to a glyphosate-peptide-2 (GLP-2) conjugate comprising a raw GLP-2 or a derivative thereof covalently linked via a non-peptide polymer and an immunoglobulin Fc fragment, wherein The C-terminus of the original GLP-2 or a derivative thereof has a thiol group, and one end of the non-peptide polymer is linked to an amino acid residue of GLP-2 other than the N-terminal amine group of GLP-2; A method of preparing the GLP-2 conjugate; a pharmaceutical composition comprising the GLP-2 conjugate; and a method of using the GLP-2 conjugate to treat or prevent intestinal disease, intestinal damage or gastrosia. Since the GLP-2 conjugate of the present invention has a significantly increased GLP-2 receptor binding affinity, it is shown to prolong the half-life in vivo and enhance the durability and stability in vitro. Thus, the GLP-2 conjugates of the invention can be administered at relatively low doses and exhibit enhanced drug compliance without fluctuating blood glucose concentrations. Therefore, the long-acting GLP-2 conjugate of the present invention can be effectively used for the prevention or treatment of intestinal diseases, intestinal damage or hyperacidity.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11530249-B2
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priorityDate 2011-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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