TABLE 1.
Compound | % inhibition at 100 μM | Published mechanism | References |
---|---|---|---|
NF279 | 95 | Suramin analogue with high selectivity for P2X over P2Y receptors; selective for P2X1 and P2X7 over other P2X receptors | 21, 54–56 |
Suramin | 95 | Broad-spectrum P2 inhibitor; also blocks calmodulin binding to recognition sites and G protein coupling to G-protein-coupled receptors | 37, 57–59 |
PPNDS | 75 | PPADS analogue with enhanced selectivity toward P2X1 | 60–63 |
NF023 | 68 | Suramin analogue with enhanced selectivity for P2X over P2Y; selectivity toward P2X1 | 59, 64, 65 |
PPADS | 38 | Broad-spectrum P2 Inhibitor | 12, 66, 67 |