Cilnidipine NEW
| Price | $41 | $81 | $134 |
| Package | 10mg | 50mg | 100mg |
| Supply Ability: | 10g |
| Update Time: | 2026-05-25 |
Product Details
| Product Name: Cilnidipine | CAS No.: 132203-70-4 |
| Purity: 99.94% | Supply Ability: 10g |
| Release date: 2026/05/25 |
Product Introduction
Bioactivity
| Name | Cilnidipine |
| Description | Cilnidipine (FRC-8653)(FRC8653) is a dual L- and N-type calcium channel blocker and displays antihypertensive, sympatholytic and neuroprotective activity. |
| In vitro | Cilnidipine inhibits the rise in blood urea nitrogen and the decline in creatinine clearance, as well as the progression of glomerulosclerosis. It prevents the increased content of renal angiotensin II, the expression of NADPH oxidase, and the augmented membrane translocation of dihydroethidium in SHR/ND rats. Administering 30 mg/kg of Cilnidipine daily to Dahl salt-sensitive rats effectively treated the elevation of systolic blood pressure. Compared to control-treated Dahl S rats, Cilnidipine reduced plasma norepinephrine levels and plasma renin activity. In spinal cord destruction rats, it suppressed the pressor responses induced by sympathetic nerve stimulation and angiotensin II. In anesthetized rats, Cilnidipine, or omega-conotoxin MVIIA, lowered mean arterial blood pressure with a slight increase in heart rate. At antihypertensive doses in rats, Cilnidipine affected sympathetic nerve N-type calcium channels (Ca(2+)), besides vascular L-type channels. Following NMDA receptor activation, Cilnidipine reduced Ca(2+) influx through N-type channels, and in rats in vivo, it protected neurons from ischemic reperfusion injury in the retina. Compared to amlodipine-treated spontaneously hypertensive rats/ND mcr-cp (SHR/ND), Cilnidipine significantly prevented the increase in fibrillary protein staining and restored the expression of podocin and nephrin in the glomeruli. |
| In vivo | Cilnidipine at 10 mM can inhibit the increase in the ratio induced by 40 mM potassium chloride, and is also effective in inhibition when treated with omega-conotoxin GVIA. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO : 262.5 mg/mL (532.97 mM), Sonication is recommended. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (4.06 mM), Sonication is recommended. Ethanol : 4.9 mg/mL (9.95 mM), Sonication is recommended. |
| Keywords | long-acting | Inhibitor | inhibit | FRC8653 | FRC 8653 | Dual L-and N-type calcium channel | dihydropyridine Ca | Cilnidipine | channel | CalciumChannel | Calcium Channel | Ca2+ channels | Ca channels | Antihypertensive |
| Inhibitors Related | Quadrol | Tricaine methanesulfonate | Nisoldipine | 2,4,6-Tri-tert-butylphenol | Chlorocresol | L-Ascorbic acid | L-Phenylalanine | L-Ascorbic acid sodium salt | 2-Nitrobenzoic acid | Magnesium Chloride Hexahydrate | Magnesium sulfate | Cinchonine |
| Related Compound Libraries | Bioactive Compound Library | Pain-Related Compound Library | Approved Drug Library | Membrane Protein-targeted Compound Library | Anti-Cancer Clinical Compound Library | Drug Repurposing Compound Library | Inhibitor Library | Neuroprotective Compound Library | Anti-Cancer Approved Drug Library | Bioactive Compounds Library Max | Ion Channel Targeted Library | Anti-Cancer Drug Library |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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