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Synthesis and anticancer potential of aminomethyl derivatives of methyl-substituted asymmetrical curcumin mono-carbonyl

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Figure

Figure 1. (A) Methoxy-substituted, (B) Methyl-substituted, and (C) Diethylaminomethyl derivatives of methyl-substituted of AMACs (Prasetyaningrum et al., 2018).
Table 2. The cytotoxicity (IC50 values) of compound 3a, 3d, 3e, 3f, curcumin, and 5-fluorouracil against MCF-7, WiDr, and Chang Liver cells
Figure 2. Cytotoxicity of compounds 3a, 3b, 3e, and 3f, curcumin (Curc) as a comparative compound, and 5-fluorouracil (5-FU) as a positive control, against MCF-7, WiDr, and Chang Liver cells

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