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Felodipine

Cat. No. M3959

All AbMole products are for research use only, cannot be used for human consumption.

Felodipine Structure
Synonym:

CGH-869

Size Price Availability Quantity
Free Sample (0.5-1 mg)  USD 0 In stock
10mM*1mL in DMSO USD 50 In stock
5mg USD 40 In stock
10mg USD 60 In stock
25mg USD 120 In stock
50mg USD 180 In stock
100mg USD 240 In stock
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Quality Control & Documentation
Biological Activity

Felodipine is widely used to study angina and hypertension. The IC50 of felodipine was ~8 nM, which was about 50 times higher than nifedipine and 430 times higher than verapamil in KCL contractile pig coronary artery segment by blocking Ca2+ channel. Filodipine significantly induced transcription and secretion of IL-6 and IL-8 in human VSMC and lung fibroblasts with ED50 values of 5.8 nM and 5.3 nM, respectively, while propranolol and furosemide did not affect the expression of these two IL-6 genes. Felodipine can block Ca2+ dependent contraction of rat ileum longitudinal smooth muscle (GPILSM) with IC50 of 1.45 nM.

Protocol (for reference only)
Cell Experiment
Cell lines
Preparation method
Concentrations
Incubation time
Animal Experiment
Animal models Male Sprague-Dawley rats with approximately 5/6 renal ablation
Formulation Dissolved in DMSO, and diluted in saline
Dosages 1 g/kg/day
Administration Orally
Chemical Information
Molecular Weight 384.25
Formula C18H19Cl2NO4
CAS Number 72509-76-3
Form Solid
Solubility (25°C) DMSO 47 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Pandey MM, et al. Pharm Dev Technol. Dissolution enhancement of felodipine by amorphous nanodispersions using an amphiphilic polymer: insight into the role of drug-polymer interactions on drug dissolution.

[2] Yiu S, et al. J Med Chem. Synthesis, biological evaluation, calcium channel antagonist activity, and anticonvulsant activity of felodipine coupled to a dihydropyridine-pyridinium salt redox chemical delivery system.

[3] Rödler S, et al. J Mol Cell Cardiol. Ca(2+)-channel blockers modulate the expression of interleukin-6 and interleukin-8 genes in human vascular smooth muscle cells.

[4] Johnson JD, et al. J Pharmacol Exp Ther. Calcium and calmodulin antagonists binding to calmodulin and relaxation of coronary segments.

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Keywords: Felodipine, CGH-869 supplier, Calcium Channel, inhibitors, activators

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