Verapamil hydrochloride NEW
| Price | $41 |
| Package | 500mg |
| Min. Order: | |
| Supply Ability: | 10g |
| Update Time: | 2025-04-28 |
Product Details
| Product Name: Verapamil hydrochloride | CAS No.: 152-11-4 |
| Purity: 99.79% | Supply Ability: 10g |
| Release date: 2025/04/28 |
Product Introduction
Bioactivity
| Name | Verapamil hydrochloride |
| Description | Verapamil hydrochloride (Verapamil HCl) is a calcium channel blocker that is a class IV anti-arrhythmia agent. |
| Cell Research | Verapamil is dissolved in DMSO and stored, and then diluted with appropriate media before use[1]. Cells (1×105) are treated with 10 nM Bortezomib and/or 70 μM Verapamil for 16 hours and incubated for another 4 hours with Alamar-Blue. Activity of the mitochondrial dehydrogenase results in conversion of the coloring, which is followed by measurement of the absorption using a spectrophotometer[1]. |
| In vitro | Verapamil exhibits antiarrhythmic properties, reduces myocardial oxygen consumption in rats, and preserves Cx43 protein. |
| In vivo | Verapamil and Diltiazem essentially inhibit the hydrolase activity of recombinant CES2, with inhibition constants (Ki) of 0.25 ± 0.02 μM and 3.84 ± 0.99 μM, respectively. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
| Solubility Information | DMSO : 50 mg/mL (101.82 mM), Sonication is recommended. H2O : 24.6 mg/mL (50.1 mM), Sonication is recommended. |
| Keywords | Verapamil hydrochloride | Verapamil Hydrochloride | Verapamil hydrochlorid | Verapamil | pressure | P-gp?(P-glycoprotein) | P-gp | Pgp | P-glycoprotein | Palbociclib | Multidrug resistance protein 1 | MDR1 | lysosomotropic | Inhibitor | inhibit | high | Cytochrome P450 | CYPs | CYP3A4 | Cluster of differentiation 243 | CD243 | CalciumChannel | Calcium Channel | Calcan Hydrochloride | Ca2+ channels | Ca channels | blood | antiarrhythmic | angina | ABCB1 | (±)-Verapamil |
| Inhibitors Related | Tebuconazole | L-Ascorbic acid | Apigenin | Fenofibrate | L-Phenylalanine | D-Menthol | Ethyl cinnamate | Naringin | L-Ascorbic acid sodium salt | Naringenin | 1-Octanol | 2-Nitrobenzoic acid |
| Related Compound Libraries | Bioactive Compound Library | Anti-Neurodegenerative Disease Compound Library | Pain-Related Compound Library | Membrane Protein-targeted Compound Library | Anti-Cancer Clinical Compound Library | Drug Repurposing Compound Library | Inhibitor Library | Anti-Cancer Approved Drug Library | FDA-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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United States- Since: 2011-01-07
- Address: 36 Washington Street, Wellesley Hill, MA
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