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 |
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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]. |
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Related Catalog | |
Target |
IC50: 3.3 nM (calmodulin)[1][2]. |
References |
Density | 1.31g/cm3 |
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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 |
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RIDADR | NONH for all modes of transport |