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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-14
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filingDate 2010-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8004e5c339fb4c909750e2fa185052ca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f1d31e95ff42f76b0a153e09f6373d7
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c19b94f6794874f5731484800b345654
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb3cc9e986b8988ffe0cf7dbb3d79191
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_27733c1db7e46f256ed90f362975383f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_02eded536fe12f5a98dd4de066cfd707
publicationDate 2014-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102548558-B
titleOfInvention Novel aminopyridine derivatives having Aurora A selective inhibitory action
abstract The present invention relates to a compound of formula (I): wherein: R1 is H or C1-2 alkyl; R2 is H or C1-3 alkyl; R3 and R4 are each independently H or C1-2 alkyl, where the alkyl may be substituted with one to three of the same or different substituents selected from R10; R5 is H, hydroxy, C1-2 alkyl, or OCH3; and R10 is F or Cl, or a pharmaceutically acceptable salt or ester thereof. The formula (I) is shown in the description.
priorityDate 2009-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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