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. 2021 Feb 19;11:4262. doi: 10.1038/s41598-021-83736-6

Table 3.

Antiproliferative activity of phytol (1) and its synthesized derivatives against selected cancer cell lines and normal mice fibroblasts.

Compound Cell lines/IC50 ± SD (μM)
MV4-11 A549 LoVo LoVo/DX BALB/3T3
IC50 (μM) IC50 (μM) IC50 (μM) IC50 (μM) IR IC50 (μM)
Phytol (1) 51.4 ± 3.6 64.1 ± 5.2 255.2 ± 46.5 70.8 ± 3.9 0.28 64.5 ± 12.9
(2) n.a n.a n.a n.a n.a
(3) 39.28 ± 5.9 49.5 ± 2.9 59.5 ± 1.1 55.03 ± 1.5 0.92 145.1 ± 48.0
(4) 46.9 ± 11.7 n.a n.a 306.3 ± 136.5 348.5 ± 27.6
(5) 52 ± 13.8 n.a n.a 261.3 ± 104.5 424 ± 140.2
(6) 48.3 ± 19.6 378.4 ± 32.8 293.4 ± 33.1 187.5 ± 32.7 0.64 273 ± 16.4
(7) 110.5 ± 41.6 n.a n.a 236.8 ± 52.9 - n.a
Cisplatin 2.88 ± 0.83 3.97 ± 1.08 5.55 ± 0.12 3.45 ± 1.01 0.62 4.44 ± 2.36
Doxorubicin - - 0.12 ± 0.01 6.53 ± 0.93

n.a. no activity in concentration of 5, 25, 125, 625 μM. IC50—compound concentration leading to 50% inhibition of cell proliferation. Data are presented as mean ± standard deviation (SD) calculated using Prolab-3 system based on Cheburator 0.4 software56. IR was calculated according to the formula IR = (IC50 estimated against resistant cell line)/(IC50 estimated against non-resistant cell line); values range: 0 < IR < 2-indicate that the tested compound is able to overcome drug resistance; 2 < IR < 10—defines the moderate ability of the compound to overcome drug resistance; IR > 10—defines no influence on the drug resistance phenomenon.