| Name | CGS 9343B,1,3-Dihydro-1-[1-[(4-methyl-4H,6H-pyrrolo[1,2-a][4,1]benzoxazepin-4-yl)methyl]-4-piperidinyl]-2H-benzimidazol-2-onemaleate |
|---|
| Description | Zaldaride maleate (CGS-9343B) is a potent and selective inhibitor of calmodulin. Zaldaride maleate (CGS-9343B) inhibits CaM (calmodulin)-stimulated cAMP phosphodiesterase activity, with an IC50 of 3.3 nM[1][2]. Zaldaride maleate (CGS-9343B) prevents estrogen-induced transcription activation by ER, reversibly blocks voltage-activated Na+, Ca2+ and K+ currents in PC12 cells and inhibits nAChR[3]. |
|---|---|
| Related Catalog | |
| Target |
IC50: 3.3 nM (calmodulin)[1][2]. |
| References |
| Density | 1.31g/cm3 |
|---|---|
| Boiling Point | 778ºC at 760 mmHg |
| Molecular Formula | C30H32N4O6 |
| Molecular Weight | 544.60 |
| Flash Point | 424.3ºC |
| Exact Mass | 544.23200 |
| PSA | 129.79000 |
| LogP | 3.85250 |
| Vapour Pressure | 1.78E-25mmHg at 25°C |
| Hazard Codes | Xi |
|---|---|
| RIDADR | NONH for all modes of transport |