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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6cbe17b80ea0cbeffc53630357beffaa
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-10
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D323-00
filingDate 2004-01-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_21a852212dbc182186878fe1f7bfea42
publicationDate 2006-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2006074251-A1
titleOfInvention Deoxoartemisinin analogs, process for their preparation, and anticancer agent comprising them
abstract The present invention relates to a new deoxoartemisinin dimer and trimer, which have excellent anticancer activity and lower toxicity and are stable to acids, to a new deoxoartemisinin monomer of intermediate thereof, to preparations thereof, and to anticancer agents comprising the deoxoartemisinin dimer or trimer.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010135427-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111372583-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2019104247-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11359112-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2021504302-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008127381-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010093651-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8884032-B2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2017173365-A1
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priorityDate 2003-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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