Activating Compound | Comment | Organism | Structure |
---|---|---|---|
2-(pyridin-4-yl)-4H-benzo[h]chromen-4-one | i.e. UCCF-029. Concentrations below 50 nM increase the open probability of the channel, favouring the channel transition to the an activated state. Levels above 50 nM determine inhibition of the channel by a reduction of the open time. UCCF-029 does not interfere with binding of ATP | Homo sapiens |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
2-(pyridin-4-yl)-4H-benzo[h]chromen-4-one | i.e. UCCF-029. Concentrations below 50 nM increase the open probability of the channel, favouring the channel transition to the an activated state. Levels above 50 nM determine inhibition of the channel by a reduction of the open time. UCCF-029 does not interfere with binding of ATP | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
isoform CFTR | - |