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. 2023 May 18;8(21):18663–18684. doi: 10.1021/acsomega.3c00554

Table 6. Cytotoxic Activity (IC50, μM) of the Studied Compounds Estimated by the MTT Assaya.

  PC3d   HaCaTe
  IC50b SIc IC50
1 68.7 ± 3.4 1.4 100.4 ± 1.2
2 85.2 ± 8.2 0.9 75.7 ± 7.5
3 2.02 ± 0.1 17.6 35.7 ± 8.2
4 51.6 ± 8.1 1.9 >100
5 97.2 ± 11.0 1.0 >100
6 107.9 ± 11.0 0.1 19.7 ± 2.8
7 >100 1 >100
8 39.6 ± 4.3 1.1 44.9 ± 9.0
9 69.1 ± 5.8 1.4 >100
10 84.1 ± 7.3 1.1 89.1 ± 2.1
11 81.7 ± 8.9 0.9 80.1 ± 8.1
12 29.7 ± 5.0 1.3 >100
13 33.7 ± 8.2 2.7 93.4 ± 10.1
14 63.4 ± 5.3 1.6 >100
15 15.7 ± 3.8 5.4 85.5 ± 9.2
16 68.8 ± 9.9 1.5 >100
17 88.4 ± 10.6 0.5 41.3 ± 5.2
18 >100 0.9 92.2 ± 8.7
19 71.4 ± 3.2 1.0 72.9 ± 5.7
20 69.9 ± 7.2 1.3 89.5 ± 5.9
21 4.8 ± 0.1 15.2 73.2 ± 10.1
CP 100.4 ± 3.6 2.2 222.1 ± 3.6
doxorubicin 0.3 ± 0.12 1.0 0.3 ± 0.11
cisplatin 13.2 ± 2.10 0.5 6.3 ± 0.70
a

Data are expressed as mean SD.

b

IC50 (μM)—the concentration of the compound that corresponds to a 50% growth inhibition of the cell line (as compared to the control) after 72 h of incubation with the individual compound.

c

The SI (selectivity index) was calculated using the formula SI = IC50 for normal cell line/IC50 cancer cell line.

d

Human metastatic prostate cancer (PC3).

e

Human immortal keratinocyte cell line from adult human skin (HaCaT).