Table 4.
Compound potency (μM) in primary screen (Mito-MPS assay), powder compound confirmation (Mito-MPS assay), imaging confirmation, and cytotoxicity assay at 1 and 5 h of treatment
| 1 h |
5 h |
||||||||
|---|---|---|---|---|---|---|---|---|---|
| Name | CASRN | Primary Screen | Confirmation | Cytotoxicity | Imaging Confirmation | Primary Screen | Confirmation | Cytotoxicity* | Imaging Confirmation |
| Apigenin | 520-36-5 | 25.91 | 7.17 ± 1.34 | inactive | 4.06 | 4.60 | 12.68 ± 3.17 | inactive | 9.49 |
| BIO | 667463-62-9 | 0.09 | 0.23 ± 0.06 | inactive | 1.83 | 0.23 | 0.42 ± 0.05 | inactive | 1.94 |
| Diphenyleneiodonium chloride | 4673-26-1 | 3.26 | 15.46 ± 5.84 | inactive | 19.87 | 1.83 | 8.05 ± 6.91 | inactive | 9.74 |
| Genistein | 446-72-0 | 25.91 | 18.10 ± 4.10 | inactive | 7.74 | 7.94 | 18.76 ± 5.70 | inactive | 12.27 |
| GW-5074 | 220904-83-6 | 7.30 | 6.43 ± 1.41 | inactive | 6.52 | 2.31 | 5.85 ± 2.07 | inactive | 7.74 |
| Indirubin-3′-oxime | 160807-49-8 | 0.25 | 0.44 ± 0.09 | inactive | 4.38 | 0.41 | 0.55 ± 0.12 | inactive | 4.35 |
| Isoliquiritigenin | 961-29-5 | 6.51 | 5.87 ± 1.88 | inactive | 3.88 | 3.66 | 10.24 ± 2.53 | inactive | 12.27 |
| Niclosamide | 50-65-7 | 0.41 | 0.72 ± 0.50 | inactive | 0.41 | 0.32 | 0.75 ± 0.46 | 1.12 (48%) | 0.52 |
| Piceatannol | 10083-24-6 | 10.31 | 5.87 ± 1.41 | inactive | 5.81 | 5.17 | 8.64 ± 2.35 | inactive | 12.27 |
| Rottlerin | 82-08-6 | 6.51 | 5.65 ± 2.59 | inactive | 1.54 | 3.26 | 4.04 ± 0.82 | 1.78 (49%) | 1.37 |
| SP-600125 | 129-56-6 | 1.15 | 2.50 ± 0.88 | inactive | 24.64 | 1.63 | 2.52 ± 0.31 | inactive | 27.47 |
| Tyrphostin 47 | 122520-86-9 | 12.59 | 7.38 ± 0.84 | inactive | 16.39 | 16.35 | 21.0 ± 4.15 | inactive | 54.8 |
| Tyrphostin A9 | 10537-47-0 | 0.07 | 0.15 ± 0.06 | inactive | 0.07 | 0.04 | 0.18 ± 0.08 | inactive | 0.11 |
| Tyrphostin AG-879 | 148741-30-4 | 0.51 | 2.22 ± 0.99 | inactive | 1.23 | 0.73 | 4.06 ± 1.99 | inactive | 1.73 |
BIO, (2′Z,3′E)-6-bromoindirubin-3′-oxime.
Efficacies are shown in parentheses.