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editorial
. 2014 Apr 2;5(6):1683–1698. doi: 10.18632/oncotarget.1849

Table 1: The inhibitory concentrations (IC50) of Strigolactone analogues for cancer cells.

Mean values are derived from 4 replicates of at least two independent experiments. The conversion between PPM and molarity is given for each analogue.

Tumor Cell Lines IC50 (ppm) at 72 h
EG5
1ppm= 2.3 μM
EG9C
1ppm=3.2 μM
ST357
1 ppm=2.5 μM
ST362
1 ppm=2.0 μM
MEB55
1 ppm = 3.1 μM
Prostate
PC3
DU145
LNCaP

>15
13
>15

>15
>15
11.5

5.0
8.5
11.4

10.3
7.5
2.5

8.8
10.8
2.99
Colon
HT-29
HCT116
SW480

>15
>15
>15

>15
>15
>15

>15
>15
>15

7.3
5.2
2.9

8.2
10.4
9.7
Lung
A549

4.7

15.5

4.9

5.2

5.1
Osteosarcoma
U20S

3.9

4.5

4.5

2.8

2.7
Non-tumor cells
BJ Fibroblasts


ND


>20


>20


ND


>20