Table 5.
Reported bd oxidase inhibitors.
Compound | Microorganism targeted | IC50 | Bacterial inhibition | Toxicity | Inhibition mechanism |
---|---|---|---|---|---|
| |||||
Aurachin D | E. coli | 18 nM (Radloff et al. 2021) | >128 μg/mL (MIC) (Dejon and Speicher 2013) | HCT-116 1 μg/mL (GI50) U-2 OS 1 μg/mL (GI50) U937 1 μg/mL (GI50) (Dejon and Speicher 2013) |
Blocking of quinone binding site (Miyoshi et al. 1999; Grauel et al. 2021) |
ND-01192 | E..coli | 0.6–1.3 μM (Kägi et al. 2023) | Mt Complex I IC50 3 μM (Kägi et al. 2023) | ||
CK-2–63 | M. tuberculosis | 3 nM (Jeffreys et al. 2023) | 37.8% at 5 μM (Jeffreys et al. 2023) | HepG2 IC50 85 μM 181 | Blocking of quinone binding site (Jeffreys et al. 2023) |