New 2-Acetyl-3-aminophenyl-1,4-naphthoquinones: Synthesis and <i>In Vitro</i> Antiproliferative Activities on Breast and Prostate Human Cancer Cells

<div>Typical cyclic voltammogram of compound 23 in 0.1 M Et<sub>4</sub>NBF<sub>4</sub>/acetonitrile obtained in Pt electrode, scan rate 100 mV/s. The cathodic (c) and anodic (a) peaks are indicated in the figure.</div>

Oxidative Medicine and Cellular Longevity

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Figure 4

Figure 4: New 2-Acetyl-3-aminophenyl-1,4-naphthoquinones: Synthesis and <i>In Vitro</i> Antiproliferative Activities on Breast and Prostate Human Cancer Cells 

Figure 4 | New 2-Acetyl-3-aminophenyl-1,4-naphthoquinones: Synthesis and In Vitro Antiproliferative Activities on Breast and Prostate Human Cancer Cells 