http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008114976-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K7-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-06
filingDate 2008-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb03cc5d7aabb2ac760803c0fffd5890
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f5aa3da390ef81f00ba9572ae712615c
publicationDate 2008-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2008114976-A1
titleOfInvention Spinorphin derivatives as potent and selective human p2x3 receptor antagonist
abstract The present invention relates to a spinorphin derivative useful as a potent and selective human P2X<SUB>3</SUB> receptor antagonist. More particularly, the present invention provides a spinorphin derivative useful as a potent and selective human P2X<SUB>3</SUB>receptor antagonist selected from peptide AVVYPWT, peptide LAVYPWT, peptide LVAYPWT, peptide LVVAPWT and/ or cyclic peptide LWYPWT. Human P2X<SUB>3</SUB> receptor antagonist has been developed on the electrophysiological evaluation of spinorphin peptide derivatives, truncated peptide analogues, cyclic peptides and a retroinverso peptide at human P2X<SUB>3</SUB> receptors to determine the channel blocking activity.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010062159-A1
priorityDate 2007-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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