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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

Chalcone

R’

B

1

2′,4′,6′-Trimethoxy-

3,4-Dimethoxyphenyl-

2

2′,5′-Dimethoxy-

4-Methoxyphenyl-

3

2′,5′-Dimethoxy-

3,4-Methylenedioxyphenyl-

4

3′,4′,5′-Trimethoxy-

4-Fluorophenyl-

5

3′,4′,5′-Trimethoxy-

4-Dimethylaminophenyl-

6

3′,4′,5′-Trimethoxy-

4-Methoxyphenyl-

7

3′,4′,5′-Trimethoxy-

3,4-Dimethoxyphenyl-

8

3′,4′,5′-Trimethoxy-

3,4-Methylenedioxyphenyl-

9

4′-Chloro-

1H-Indole-2-yl-

10

4′-Iodo-

1H-Indole-2-yl-