| Product Name | (R,S)-Niguldipine HCl | 
| Description | Ca2+ channel blocker | 
| Purity | >98% | 
| CAS No. | 119934-51-9 | 
| Molecular Formula | C36H39N3O6•HCl | 
| Molecular Weight | 646.18 | 
| Field of Use | Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only. | 
| Storage Temperature | -20ºC | 
| Shipping Temperature | Shipped Ambient | 
| Product Type | Inhibitor | 
| Solubility | Soluble to 10 mM in water | 
| Source | Synthetic | 
| Appearance | Yellow solid | 
| Safety Phrases | Classification: Caution: Substance not yet fully tested. Safety Phrases: S22 - Do not breathe dust S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection S24/25- Avoid contact with shin and eyes | 
| Cite This Product | (R, S)-Niguldipine HCl (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-319) | 
| Alternative Names | (R,S)-1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid, 3-(4,4-diphenyl-1-piperidinyl)propyl methyl ester hydrochloride | 
| Research Areas | Calcium Channels, Ion Channels, Neuroscience, Voltage-Gated Calcium Channels | 
| Scientific Background | Niguldipine is a calcium channel blocker and alpha1-adrenergic receptor antagonist. In neuroscience, its dual action on calcium influx and adrenergic signaling makes it a candidate for studying neurovascular coupling and synaptic transmission. Its modulation of intracellular calcium dynamics may have implications for neurodegenerative disease models involving calcium dysregulation. | 
| References | 1. Boer R., Grassegger A., Schudt C., Glossman H. (1999) Eur J Pharmacol. 172(2): 131-145. 2. Robinson J.P., Kendall D.A. (1990) Br J Pharmacol. 100(1): 3-4. | 
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