http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20060127901-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-14
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
filingDate 2004-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad30f409b3b7aafcd30610666d4bfedb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22ade05927631e25fd93ee976fa8ddc3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d5a12f5ee0400ffcb6c679daf09a74f
publicationDate 2006-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20060127901-A
titleOfInvention Amide Derivatives and Medicines
abstract An object of the present invention is to provide an amide derivative or salt thereof having excellent inhibitory activity of BCR-ABL tyrosine kinase.n n n The present invention comprises an amide derivative represented by the following formula (1) or a salt thereof and a pharmaceutical composition comprising these as an active ingredient:n n n n Formula 1n n n n n n n n n In the formula, R 1 represents -CH 2 -R 11 (R 11 represents a nitrogen-containing saturated heterocyclic group) and the like, R 2 represents alkyl, halogen, haloalkyl and the like, R 3 represents hydrogen and the like, Het1 is And the like, and Het2 represents pyrimidinyl and the like.n n n The compounds of the present invention are useful as BCR-ABL tyrosine kinase inhibitors.
priorityDate 2003-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 572.