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Q59237520-0E351EF4-8BE9-4309-B9C5-EBF2A52D6F43
Q59237520-0E351EF4-8BE9-4309-B9C5-EBF2A52D6F43
BestRank
Statement
http://www.wikidata.org/entity/statement/Q59237520-0E351EF4-8BE9-4309-B9C5-EBF2A52D6F43
Isolation, biological activity and synthesis of the natural product ellipticine and related pyridocarbazoles
P2860
Q59237520-0E351EF4-8BE9-4309-B9C5-EBF2A52D6F43
BestRank
Statement
http://www.wikidata.org/entity/statement/Q59237520-0E351EF4-8BE9-4309-B9C5-EBF2A52D6F43
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Statement
wasDerivedFrom
4e028a831e151ad1a0d4d05166d671937274d140
P2860
The anticancer drug ellipticine forms covalent DNA adducts, mediated by human cytochromes P450, through metabolism to 13-hydroxyellipticine and ellipticine N2-oxide.