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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-1077
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-7155
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-715
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-107
filingDate 1998-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_74aeb2fd813cc7b806d97cce51d1371b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55c251ff0302346a66794ffba13222cd
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publicationDate 1998-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2277011-A1
titleOfInvention Membrane-permeable derivatives converted intracellularly into active peptides
abstract The present invention relates to membrane-permeable peptides which are intracellular agonists and/or antagonists of chemotactic factor receptors are rendered hydrophobic through acylation and acetoxymethylation of their amine and acid functional groups. The modified peptides of the present invention are loaded into cells. The acetoxymethyl esters are cleaved by non-specific esterases rendering the peptides active in the intracellular compartments of the cells. The effects of the introduction of transformed specific peptides corresponding to intracellular regions common to the major chemokine receptors are illustrated. These peptides completely inhibited chemotactic factor and chemokine-induced calcium mobilization. Furthermore, leukocytes of mice intravenously injected with these peptides failed to migrate towards chemokines(IL-8).
priorityDate 1997-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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