http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7276576-B1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-06
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H21-04
filingDate 1997-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a789a5cc7682e191baa73458d4c62b68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_886e18e3951eda5eaca243be8461188f
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publicationDate 2007-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7276576-B1
titleOfInvention Mammalian ICYP (iodocyanopindolol) receptor and its applications
abstract An isolated and substantially pure mammal polypeptide different from known adrenergic, serotonine and dopamine receptors, existing at least on mammalian muscle and eosinophils membranes, for instance in rat, guinea pig and humans. The invention also relates to plasmids containing the genes coding for said polypeptide, to host cells transformed by genes coding for the above mentioned polypeptide, to nucleotide probes capable of hybridizing with the genes coding for the above mentioned polypeptide, and to polyclonal and monoclonal antibodies directed against the above mentioned polypeptide. Said polypeptide is characterized in that it contains sites such that when said sites are exposed at the surface of a cell, they are able of binding iodocyanopindolol (ICYP) under blockage of α, β1, β2, β3-AR, serotonine 5-HT 1A and serotonine 5-HT 1B receptors, said binding being saturable, reversible, able to be displaced by a β-adrenergic receptor agonist SM-11044 with stereoselectivity but not by isoproterenol, norepi-nephrine, epinephrine, serotonine, dopamine or BRL-37344, and not being blocked by propranolol, said polypeptide (1) having an apparent molecular weight of about 30-40 kDa when labeled with 125 I-iodocyanopindolol after photoaffinity labeling and separation by electrophoresis and an apparent molecular weight of about 60-80 kDa in Western blot, and (2) generating a fragment having the following formula DPX 1 FFQHRIHX 2 FSIFNX 3 by acidic cleavage, wherein X 1 represents S (SEQ ID NO.5) or X (SEQ ID NO.6), X 2 represents V (SEQ ID NO.6) or W (SEQ ID NO.5) and X 3 represents S (SEQ ID NO.5) or H (SEQ ID NO.6), said polypeptide being present at least on muscles and eosinophils membranes and being a non-adrenergic receptor.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8927589-B2
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priorityDate 1996-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129225149
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ295T3
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4828
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7021821
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID248
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226409332
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129143706
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1255525
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9RLA0
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10476
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCO93745
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8097
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9RLB6
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226457254

Total number of triples: 313.