Table 1.
Pharmacological stimuli.
Compound | Target | Mechanism | Specificity | Source | Vehicle | Conc. | Incubation time (h) | Ref. |
---|---|---|---|---|---|---|---|---|
MG132 | Proteasome | Binds the ß5 20 S subunit | +++ | Sigma #C2211-5MG | DMSO | 10 µM | 18 h | 53,54 |
VER155088 | HSP70 | Binds the ATPase domain | +++ | Sigma #SML0271 | DMSO | 20 µM | 18 h | 8,55 |
Staurosporine | Kinases | Non-selective ATP-competitive inhibitor | ++ | AbCam #ab146588 | DMSO | 500 nM | 2 h | 56,57 |
Celastrol | Heat shock response | Activation of HSF1 transcriptional regulation | + | Sigma #0869 | DMSO | 5 µM | 18 h | 22,58,59 |
Novobiocin | HSP90 | Binds the ATP-binding site of the ATPase subunit | + | Sigma #N1628 | mQ | 800 µM | 6 h | 26,55 |
Compounds were diluted into fresh culture media before incubation at 37 °C. Compounds are categorized as poor (+), moderate (++), and high (+++) specificity according to the scope of the target and reported range of off-target effects.