http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100392468-B1

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Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-30
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-04
filingDate 2000-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2003-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2003-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100392468-B1
titleOfInvention 3-Hydroxychromene-4-on derivatives useful as cyclin dependendent kinase inhibitors
abstract The present invention relates to 3-hydroxychromen-4-one derivatives of the general formulas (1), (2) or (3) below, which are useful as inhibitors of cyclin dependent kinases (CDKs), pharmaceutically acceptable salts, hydrates, solvates and isomers thereof. . The present invention also provides a method for preparing a compound of formula 1, 2 or 3 and cancer, inflammation, vascular stenosis, characterized in that it contains a compound of formula 1, 2 or 3 as an active ingredient together with a pharmaceutically acceptable carrier and The present invention relates to inhibitors and therapeutic agents for diseases related to cell proliferation such as angiogenesis.n n n [Formula 1]n n n n n n n n [Formula 2]n n n n n n n n [Formula 3]n n n n n n n n In the above formula,n n n R 1 is hydrogen, alkyl, amino alkyl or hydroxy alkyl group,n n n R 2 is hydrogen, methyl, trifluoromethyl or halogen,n n n R3 represents an alkyl, amino alkyl or hydroxy alkyl group,n n n X represents a halogen.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100614379-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101178894-B1
priorityDate 2000-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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