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Nicardipine hydrochloride

Catalog No. T1215Cas No. 54527-84-3
Alias YC-93 Hydrochloride, RS-69216, Nicardipine HCl

Nicardipine hydrochloride (YC-93 Hydrochloride) is the hydrochloride salt form of nicardipine, a synthetic derivative of nitrophenyl-pyridine and potent calcium channel blocker, Nicardipine (Nifedipine Family) blocks calcium ions from certain cell walls and inhibits contraction of coronary and peripheral arteries, resulting in lowered oxygen requirements for heart muscle and decreased arterial contraction and spasm. It is used clinically as a cerebral and coronary vasodilator.

Nicardipine hydrochloride

Nicardipine hydrochloride

Purity: 100%
Catalog No. T1215Alias YC-93 Hydrochloride, RS-69216, Nicardipine HClCas No. 54527-84-3
Nicardipine hydrochloride (YC-93 Hydrochloride) is the hydrochloride salt form of nicardipine, a synthetic derivative of nitrophenyl-pyridine and potent calcium channel blocker, Nicardipine (Nifedipine Family) blocks calcium ions from certain cell walls and inhibits contraction of coronary and peripheral arteries, resulting in lowered oxygen requirements for heart muscle and decreased arterial contraction and spasm. It is used clinically as a cerebral and coronary vasodilator.
Pack SizePriceAvailabilityQuantity
500 mg$41In Stock
1 g$48In Stock
1 mL x 10 mM (in DMSO)$45In Stock
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Purity:100%
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Product Introduction

Bioactivity
Description
Nicardipine hydrochloride (YC-93 Hydrochloride) is the hydrochloride salt form of nicardipine, a synthetic derivative of nitrophenyl-pyridine and potent calcium channel blocker, Nicardipine (Nifedipine Family) blocks calcium ions from certain cell walls and inhibits contraction of coronary and peripheral arteries, resulting in lowered oxygen requirements for heart muscle and decreased arterial contraction and spasm. It is used clinically as a cerebral and coronary vasodilator.
Targets&IC50
Ca2+ channel (Cardiac):1 μM (IC50)
In vitro
Nicardipine significantly reduced systolic blood pressure in spontaneously hypertensive rats. In spontaneously hypertensive rats, Nicardipine significantly decreased the intima-media thickness and increased the lumen area at the level of cerebral arteries and small molluscum arteriosum.Nicardipine increased the number of neurons in the occipital cortex and frontal cortex in the SHR and inhibited the proliferation and hypertrophy of GFAP-positive astrocytes.Nicardipine also increased the number of neurons in the CA1 area of the hippocampus. increase in the number of neurons in the CA1 region of the hippocampus and reduced the size and number of astrocytes in gray and white matter. Nicardipine (5 mg/kg) in combination with flunarizine (80 mg/kg) and nimodipine (80 mg/kg) significantly potentiated the protective effect of ethosuximide (50 mg/kg) or valproic acid (100 mg/kg) against clonic seizures in mice. Nicardipine (40 mg/kg, 2 times/day for 8 weeks) reduced plaque area by 49.2% in rabbits (cholesterol-fed).Nicardipine (40 mg/kg) reduced aortic cholesterol accumulation in cholesterol-fed rabbits by 74.5%.Nicardipine (100 mg/kg) caused a significant transient reduction in cat Nicardipine (100 mg/kg) caused a significant transient reduction in retinal blood flow in cats. Although Nicardipine (100 mg/kg) decreased mean arterial blood pressure in cats, it significantly increased blood flow to the ONH, suggesting that Nicardipine benefits optic nerve hypoplasia tissue.
AliasYC-93 Hydrochloride, RS-69216, Nicardipine HCl
Chemical Properties
Molecular Weight515.99
FormulaC26H30ClN3O6
Cas No.54527-84-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 45 mg/mL (87.21 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9380 mL9.6901 mL19.3802 mL96.9011 mL
5 mM0.3876 mL1.9380 mL3.8760 mL19.3802 mL
10 mM0.1938 mL0.9690 mL1.9380 mL9.6901 mL
20 mM0.0969 mL0.4845 mL0.9690 mL4.8451 mL
50 mM0.0388 mL0.1938 mL0.3876 mL1.9380 mL

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