http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004259166-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-9121
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-1205
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-54
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filingDate 2004-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd1790f1030a29c75b4afa29d1d162da
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d5514214f5ba4fcf609e6e6862e44261
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ab2779a1b87439dca650839ec6280c3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f95d8ef015a4bc11552a06d8aeef08ec
publicationDate 2004-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004259166-A1
titleOfInvention Methods for designing inhibitors of serine/threonine kinases and tyrosine kinases
abstract The invention relates to methods for designing inhibitors of serine/threonine kinases and tyrosine kinases, particularly MAP kinases, through the use of ATP-binding site mutants of those kinases. The methods of this invention take advantage of the fact that the mutant kinases are capable of binding inhibitory compounds of other kinases with greater affinity than the corresponding wild-type kinase. The invention further relates to the mutant kinases themselves and crystallizable co-complexes of the mutant kinase and the inhibitory compound.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8097408-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2009170720-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8673268-B2
priorityDate 1998-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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