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. 2015 Nov 11;108:79–88. doi: 10.1016/j.ejmech.2015.11.009

Table 2.

Cytotoxicity (IC50-μM) of ferruginol (1) and analogues 514 on HeLa, Jurkat, U937 and Vero cell lines.

Compound Cell linesc
HeLa
Jurkat
U937
Vero
IC50a (μM) SIb IC50a (μM) SIb IC50a (μM) SIb IC50a (μM)
1 64.9 1.4 48.2 1.9 21.3 4.2 90.4
5 >50 NA >50 NA >50 NA NE
6 >80 NA 49.4 0.8 >80 NA 39.8
7 >50 NA 30.9 2.7 36.0 2.3 82.5
8 >50 NA >50 NA >50 NA NE
9 60.0 1.5 21.6 4.2 33.2 2.7 90.8
10 29.0 9.2 21.9 12.2 >40 NA 266.8
11 >40 NA >40 NA >40 NA NE
12 7.3 >43.8 12.3 >26.0 8.3 >38.5 >320
13 >30 NA >30 NA >30 NA NE
14 >30 NA >30 NA >30 NA NE
PXT 0.099 NA 0.0005 NA 0.006 NA 0.65
DOX 0.834 NA 0.012 NA 0.077 NA 1.93

PXT: Paclitaxel; DOX: Doxorubicine. NA: Not apply; NE: Not evaluated. These values represent the geometric mean of two independent experiments, each one made by quadruplicate.

a

Inhibitory concentration 50 defined as concentration of compounds that induces 50% of growth inhibition at 48 h.

b

SI, selectivity index defined as VERO IC50 over either Jurkat, U937 or HeLa IC50.

c

Jurkat, human acute T cell leukemia ATCC TIB-152; U937, human promonocytic cell line ATCC CRL-1593.2; HeLa, human cervix epitheloid adenocarcinoma cells ATCC CRL-1958; Vero, Cercopithecus aethiops African green monkey kidney cells ATCC CCL-81.