Research Article
Novel Thioethers of Dihydroartemisinin Exhibiting Their Biological Activities
Table 3
In vitro cytotoxic activity of the synthesized conjugates.
| No. | Compounds | IC50 (μM) | Hep-G2 | LU-1 |
| 1 | 5a | 10.76 ± 0.13 | 41.73 ± 0.59 | 2 | 5b | 11.33 ± 0.65 | 41.90 ± 0.25 | 3 | 5c | — | — | 4 | 5d | 5.75 ± 0.51 | 21.90 ± 0.14 | 5 | 5e | 5.70 ± 0.33 | 20.86 ± 0.09 | 6 | 5f | 6.34 ± 0.10 | 22.36 ± 0,24 | 7 | 5g1 | — | — | 8 | 5h | 2.73 ± 0.06 | 13.06 ± 0,15 | 9 | 5i | 11.09 ± 0.32 | 33.74 ± 0,51 | 10 | 5k1 | 10.43 ± 0.30 | 38.60 ± 0,29 | 11 | DHA | 21.00 ± 0.91 | 79,63 ± 0.68 | 12 | Ellipticine | 1.06 ± 0,05 | 1.38 ± 0,12 |
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Ellipticine (Merck, Germany) was employed as a positive control. |