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Table 1 Structure of the synthesized chalcones 1–10

From: In vitro anti-malarial efficacy of chalcones: cytotoxicity profile, mechanism of action and their effect on erythrocytes

ChalconeR’B
12′,4′,6′-Trimethoxy-3,4-Dimethoxyphenyl-
22′,5′-Dimethoxy-4-Methoxyphenyl-
32′,5′-Dimethoxy-3,4-Methylenedioxyphenyl-
43′,4′,5′-Trimethoxy-4-Fluorophenyl-
53′,4′,5′-Trimethoxy-4-Dimethylaminophenyl-
63′,4′,5′-Trimethoxy-4-Methoxyphenyl-
73′,4′,5′-Trimethoxy-3,4-Dimethoxyphenyl-
83′,4′,5′-Trimethoxy-3,4-Methylenedioxyphenyl-
94′-Chloro-1H-Indole-2-yl-
104′-Iodo-1H-Indole-2-yl-