http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013173679-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2e85961bb2dd7bc5dc990953233d799e
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-407
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-052
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-551
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5377
filingDate 2012-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0518c15aa66f4a97001ace55ed8c6b48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_066f0fe2f776dcb8c9071bbe287a3754
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8de91f13389fe71e564186cd5aac1962
publicationDate 2013-09-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2013173679-A
titleOfInvention Novel chromenoindole derivative, method for producing the derivative, and anticancer agent containing the derivative
abstract A compound having excellent antitumor activity is provided. A chromenoindole derivative (A) represented by the formula (A) or a pharmaceutically acceptable salt thereof. In the formula (A), R 1 is a halogen, an alkyl group or an alkoxy group, n is an integer of 0 to 4, and R 2 is a specific substituted amino group or a cyclic amino group. [Selection figure] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102373435-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20160111595-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108276420-A
priorityDate 2012-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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