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. Author manuscript; available in PMC: 2019 Mar 20.
Published in final edited form as: Bioorg Med Chem. 2010 Mar 31;18(10):3481–3493. doi: 10.1016/j.bmc.2010.03.070

Table 3.

Inhibition values (IC50, lM) of several verticipyrone analogues determined by MTT assay using human and mouse cell linesa

Compound MCF-7 MCF-10A CRL-2365 CRL-2366 A549 3LL
1 23.2 ± 0.6 9.9 ± 0.3 29.9 ± 0.6 >31 20.7 ± 0.6 22.2 ± 5
12 >31 >31 >31 >31 >31 >31
13 >31 >31 >31 >31 >31 >31
14 >31 >31 >31 >31 >31 >31
16 3.3 ± 0.3 5.3 ± 0.3 3.3 ± 2.4 2.7 ± 0.3 5.3 ± 0.1 0.39 ± 0.07
17 3.3 ± 0.3 5.6 ± 0.3 2.4 ± 0.3 3.3 ± 1.5 4.1 ± 0.3 0.34 ± 0.05
18 >31 >31 >31 >31 >31 >31
28 >27 15.1 ± 0.8 >27 >27 >27 17.3 ± 1.7
30 17.4 ± 0.9 9.2 ± 0.2 12.4 ± 0.9 19.5 ± 0.7 17.0 ± 0.9 13.5 ± 0.2
a

Cell Type: MCF-7 (breast carcinoma); MCF-10A (‘normal’ human breast); CRL-2365 (brain glioblastoma); CRL-2366 (DNA repair deficient brain glioblastoma); A549 (lung carcinoma); 3LL (mouse Lewis lung carcinoma). DMSO was used as vehicle in the testing.