http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2018173409-A

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filingDate 2018-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3688e2b8e5da96bbd94421660679a491
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2720522f4fa41a0227b1b4ae68455406
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ce4e78035ca56c6c82d848b4415215e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd53f3c98da2efb97bf79f789e6f7e0d
publicationDate 2018-11-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2018173409-A
titleOfInvention Cell-free PYRIN inflammasome / NOD2 nodosome reconstruction drug discovery technology
abstract Disclosed is a compound that modulates the function of a NOD-like receptor family, for example, PYRIN inflammasome / NOD2 nodosome, and is effective for the treatment and / or prevention of related diseases. SOLUTION: PYRIN and ASC constituting a PYRIN inflammasome are synthesized by wheat cell-free protein synthesis technology, combined with an amplified luminogenic proximity assay, and an in vitro cell-free PYRIN inflammasome reconstitution system is constructed. Nod2 and RIPK2 composing NOD2 nodosome were synthesized by wheat cell-free protein synthesis technology, combined with amplified luminous proximity assay to construct in vitro in vitro cell-free NOD2 nodosome reconstitution system and PYRIN inflammasome The compound to modulate. [Selection figure] None
priorityDate 2017-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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