http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1290447-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f07ba5e7ff356b7eda43fdfc20eef4b0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-9406
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-107
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filingDate 2001-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14ade8a674a38a22b22573d8a06a1fdc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d12e0f5c07919bca78c7731578eb1861
publicationDate 2005-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1290447-B1
titleOfInvention Peptide potentiation of acid-sensory ion channel in pain
abstract An assay for determining agonists, antagonists, or modulators for acid-sensing ion channels. The assay is especially useful for screening analgesics. The screening assay can be provided in a kit form. The assay comprises administering the composition to be screened to cells expressing acid-gated channels and then determining whether the composition inhibits, enhances, or has no effect on the channels when acid is introduced. The determination can be performed by analyzing whether a current is sustained by the cells in the presence of the composition and the acid. This current can be compared to that sustained by the FMRFamide and related peptides.
priorityDate 2000-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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