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. Author manuscript; available in PMC: 2016 Jun 5.
Published in final edited form as: Chem Biol Interact. 2014 Nov 21;234:154–161. doi: 10.1016/j.cbi.2014.11.010

Figure 1.

Figure 1

Two-electron reduction of doxorubicin to the putative cardiotoxic alcohol metabolite, doxorubicinol, at the 13th carbon. NADPH-dependent monomeric carbonyl reductase CBR1 is known to mediate this reaction. Here, we demonstrate that this reaction is also carried out by a protein that shares high sequence identity with Cbr1, carbonyl reductase 3.