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filingDate 1999-08-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a2411bdc5bb109f7f025656260ee3f5a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ea1b4cc3e81bf10da9146b0c6732777
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e51a79609fec341b2d3475e9809f989
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6181a46977e99129787c67535b221414
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b3eb650817635f0dff5a560c1a3ca299
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1c4c0c9d175b6930737197175c277172
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aefac0bfcaa76d5d4b976b4c58d30730
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e4b40f2760ed4d7cf2220f4bf4c6ea6c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8e3359dc8d946038a9b7d42068a99cf8
publicationDate 2001-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1109800-A1
titleOfInvention Novel cdk inhibitors having flavone structure
abstract The present invention relates to a novel flavone derivative, pharmaceutically acceptable salt, hydrate, solvate and isomer thereof which is useful as an inhibitor against Cyclin Dependent Kinase (CDK), a process for preparation thereof, and a composition of anti-cancer agent or agent for treating neurodegenerative disease comprising this compound as an active ingredient.
priorityDate 1998-09-01-04:00^^<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/protein/ACCF1MA87
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Total number of triples: 1009.