Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2334 |
Avanafil
阿伐那非,TA1790 |
PDE | Metabolism |
Avanafil (TA1790) 是一种高活性PDE-5抑制剂,IC50=5.2 nM,对PDE1,PDE6和PDE11活性较低。 | |||
T37181 |
Avanafil metabolite M4
Avanafil metabolite M4 |
||
Avanafil metabolite M4 is a major active metabolite of the phosphodiesterase 5 (PDE5) inhibitor avanafil . Avanafil is metabolized by the cytochrome P450 (CYP450) isoforms CYP3A4 and CYP2C to the major metabolites avanafil metabolite M4 and avanafil metabolite M16 , as well as minor metabolites. Avanafil metabolite M4 inhibits PDE5 with 18% of the potency of avanafil. | |||
T37180 | Avanafil metabolite M16 | ||
Avanafil metabolite M16 is a major inactive metabolite of the phosphodiesterase 5 (PDE5) inhibitor avanafil . Avanafil is metabolized by the cytochrome P450 (CYP450) isoforms CYP3A4 and CYP2C to the major metabolites avanafil metabolite M16 and avanafil metabolite M4 , as well as minor metabolites. | |||
T83536 |
(R)-Avanafil
(R)-TA1790 |
||
(R)-Avanafil ((R)-TA1790),为选择性PDE5抑制剂,IC50值为5.2 nM,主要用于勃起功能障碍研究。 | |||
T69432 |
Avanafil dibesylate
|
||
Avanafil dibesylate is a PDE5 inhibitor. |