Table 3.
Structure and mechanism of hRR subunit inhibitors.
| Structure | Name | RR Subunit Targeted | Mechanism of RR Inhibition |
|---|---|---|---|
|
P6 | RR1 | Prevents binding of the RR2 subunit |
|
P7 | RR1 | Prevents binding of the RR2 subunit |
|
p-Alkoxyphenols | RR2 | Quenches the tyrosyl radical |
|
ADP-S-HBES-S-dGTP | RR1 | Targets the S-site |
|
A167 | RR1 | Compeites with ATP to bind the A-site |
|
5-NITP | RR1 | S-site inhibitor that prevents RR1 hexamerization |
|
DHS | RR2 | Induces degradation of RR2 proteosome degredation pathway |
|
OxolsolndoLys | RR1 | Induces formation of inactive a6 hexamers |
|
NSAH | RR1 | Reversible C-site inhibitor |
|
TP6 | RR1 | Reversible C-site inhibitor |
|
NSC73735 | RR1 and RR2 | Prevents alpha subunit hexamerization and quenches the tyrosyl radical of RR2 |
|
Ti(HBED) | RR2 | Depletes intracellular labile iron pools by transmetalation |
|
Ti(Deferasirox)2 | RR2 | Depletes intracellular labile iron pools by transmetalation |