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. Author manuscript; available in PMC: 2014 Aug 28.
Published in final edited form as: Cancer Lett. 2013 May 17;337(1):77–89. doi: 10.1016/j.canlet.2013.05.017

Table 2.

IC50 values for oncology drugs tested on SUM149 cells in qHTS and confirmation MTT and Hoechst assays.

qHTS MTTa IC50
(μM)
Confirmation
MTTb IC50
(μM)
Hoechstc IC50
(μM)
Drug classd
Dactinomycin <0.02 0.027 <0.02 Antineoplastic
antibiotic
Plicamycin <0.02 0.028 0.12 r Antineoplastic
antibiotic
Bortezomib <0.02 0.029 <0.02 Proteosome
inhibitor
Doxorubicin <0.02 0.70 <0.05 Anthracycline
Daunorubicin <0.02 0.25 0.04 Anthracycline
Fludarabine 2.1 ± 1.1 0.48 0.45 Antimetabolite
Mitoxantrone 2.5 ± 0.6 3.08 0.20 Anthracenedione
antineoplastic
antibiotic
Sorafenib 4.5 ± 0.4 3.93 8.69 Kinase inhibitor
Sunitinib 5.0 ± 0.8 5.55 6.10 Kinase inhibitor
Gefitinib 6.2 ± 2.3 7.27 14.10 Kinase inhibitor
Vorinostat 8.9 ± 4.9 2.44 2.02 HDAC inhibitor
Lapatinib 9.0 ± 0.3 10.85 6.73 Kinase inhibitor
Mitomycin 9.1 ± 0.4 1.61 0.53 Antineoplastic
antibiotic
Bleomycin 13.8 ± 2.0 0.82 0.30 Antineoplastic
antibiotic
Capecitabine 15.0 ± 9.5 17.51 >20 Antimetabolite

aIC50 values derived from qHTS screen of complete approved oncology drug set (89 drugs originally obtained from NCI DTP in plate format). Average and SD values derived from minimum of three independent experiments. The approved oncology drugs were resourced from the NCI DTP as dry powders and retested in MTTb and Hoechstc assays as described in Materials and Methods. dSee supplementary Table 2 for full listing of drug class and mechanism of action for the approved oncology drug set.