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Technical Data
| Formula | C17H18N2O6 |
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| Molecular Weight | 346.33 | CAS No. | 21829-25-4 | |
| Solubility (25°C)* | In vitro | DMSO | 69 mg/mL (199.23 mM) | |
| Ethanol | 15 mg/mL (43.31 mM) | |||
| Water | Insoluble | |||
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
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Biological Activity
| Description | Nifedipine is a dihydropyridine calcium channel blocker, used to lower hypertension and to treat angina. | |
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| In vitro | Nifedipine causes a significant concentration-dependent increase in eNOS protein expression by cultured human coronary artery endothelial cells. [1] Nifedipine antagonizes L-type Ca+ channels found throughout the cardiovascular system, but also blocks Kv channels, which are members of the same supergene family. [2] Nifedipine dose-dependently decreases the values of [(3)H]-thymidine incorporation and total cellular protein content as well as the levels of phosphorylated extracellular signal-regulated protein kinase (ERK) 1/2, mitogen-activated protein kinase kinase (MEK) 1/2, and even the phosphorylation of Pyk2, in vascular smooth muscle cells (VSMC). Nifedipine suppresses the levels of proliferative cell nuclear antigen (PCNA) dose-dependently in both VSMC and balloon-injured thoracic aortae in VSMC. [3] | |
| In vivo | Nifedipine (3 mg/kg) slightly lowers the level of systolic and/or diastolic blood pressure or increased the heart rate in rats. [3] Nifedipine (1 μm) produces a maximal inhibition of the store-operated pathway in choroidal arteriolar smooth muscle. [4] Nifedipine (20 and 40 mg/kg) markedly prevents the HCl plus ethanol-induced gastric mucosal injury and the increase in the content of thiobarbituric acid-reactive substances in the injured mucosa in rats. Nifedipine (20 and 40 mg/kg) dose-dependently promotes the ulcer healing and inhibites the increase in the content of thiobarbituric acid-reactive substances in the ulcerated mucosa in rats. [5] |
Protocol (from reference)
References
Customer Product Validation
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Data from [Data independently produced by , , Sci Rep, 2017, 7(1):3156]
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Data from [Data independently produced by , , Biochem Biophys Res Commun, 2019, 509(1):76-81]
Selleck's Nifedipine has been cited by 13 publications
| Electrical stimulation of cochlear implant promotes activation of macrophages and fibroblasts under inflammation [ Laryngoscope Investig Otolaryngol, 2023, 8(5):1390-1400] | PubMed: 37899874 |
| Repurposing screen identifies Amlodipine as an inducer of PD-L1 degradation and antitumor immunity [ Oncogene, 2021, 40(6):1128-1146] | PubMed: 33323966 |
| Calcium channel blocker amlodipine besylate therapy is associated with reduced case fatality rate of COVID-19 patients with hypertension [ Cell Discov, 2020, 6(1):96] | PubMed: 33349633 |
| YiQiFuMai Powder Injection Attenuates Coronary Artery Ligation-Induced Heart Failure Through Improving Mitochondrial Function via Regulating ROS Generation and CaMKII Signaling Pathways. [ Front Pharmacol, 2019, 10:381] | PubMed: 31031629 |
| SAD-A, a downstream mediator of GLP-1 signaling, promotes the phosphorylation of Bad S155 to regulate in vitro β-cell functions [Wang K Biochem Biophys Res Commun, 2019, 509(1):76-81] | PubMed: 30573363 |
| Polybrene induces neural degeneration by bidirectional Ca2+ influx-dependent mitochondrial and ER-mitochondrial dynamics [ Cell Death Dis, 2018, 9(10):966] | PubMed: 30237514 |
| Polybrene induces neural degeneration by bidirectional Ca2+ influx-dependent mitochondrial and ER-mitochondrial dynamics [ Cell Death Dis, 2018, 9(10):966] | PubMed: 30237514 |
| Long-term presence of angiotensin II type 1 receptor autoantibody reduces aldosterone production by triggering Ca2+ overload in H295R cells [Lei J Immunol Res, 2018, 66(1):44-51] | PubMed: 29147891 |
| Dual effects of fructose on ChREBP and FoxO1/3α are responsible for AldoB up-regulation and vascular remodelling [ Clin Sci (Lond), 2017, 131(4):309-325] | PubMed: 28007970 |
| Modeling Congenital Hyperinsulinism with ABCC8-Deficient Human Embryonic Stem Cells Generated by CRISPR/Cas9. [Guo D, et al. Sci Rep, 2017, 7(1):3156] | PubMed: 28600547 |
RETURN POLICY
Selleck Chemical’s Unconditional Return Policy ensures a smooth online shopping experience for our customers. If you are in any way unsatisfied with your purchase, you may return any item(s) within 7 days of receiving it. In the event of product quality issues, either protocol related or product related problems, you may return any item(s) within 365 days from the original purchase date. Please follow the instructions below when returning products.
SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.
NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.