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Nifedipine
[CAS# 21829-25-4]

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Complete supplier list of Nifedipine
Identification
Classification API >> Circulatory system medication >> Prevention and treatment of angina pectoris
Name Nifedipine
Synonyms Dimethyl 1,4-dihydro-2,6-dimethyl-4-(2'-nitrophenyl)-3,5-pyridinedicarboxylate; 1,4-Dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5-pyridinedicarboxylic acid dimethyl ester
Molecular Structure CAS # 21829-25-4, Nifedipine, Dimethyl 1,4-dihydro-2,6-dimethyl-4-(2'-nitrophenyl)-3,5-pyridinedicarboxylate, 1,4-Dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5-pyridinedicarboxylic acid dimethyl ester
Molecular Formula C17H18N2O6
Molecular Weight 346.34
CAS Registry Number 21829-25-4
EC Number 244-598-3
SMILES CC1=C(C(C(=C(N1)C)C(=O)OC)C2=CC=CC=C2[N+](=O)[O-])C(=O)OC
Properties
Solubility 69 mg/mL (DNSO), <1mg/mL (water) (Expl.)
Density 1.3±0.1 g/cm3, Calc.*
Melting point 174 ºC (Expl.)
Index of Refraction 1.559, Calc.*
Boiling Point 475.3±45.0 ºC (760 mmHg), Calc.*
Flash Point 241.2±28.7 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol symbol   GHS07;GHS08 Warning    Details
Hazard Statements H302-H361    Details
Precautionary Statements P203-P264-P270-P280-P301+P317-P318-P330-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Reproductive toxicityRepr.2H361
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.4H312
Specific target organ toxicity - single exposureSTOT SE3H335
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Flammable solidsFlam. Sol.2H228
Specific target organ toxicity - repeated exposureSTOT RE1H372
Self-heating substances or mixturesSelf-heat.2H252
Acute toxicityAcute Tox.3H301
Reproductive toxicityLact.-H362
Specific target organ toxicity - single exposureSTOT SE1H370
SDS Available
up Discovory and Applicatios
Nifedipine is a dihydropyridine calcium channel blocker that was first synthesized in the late 1960s as part of research into cardiovascular drugs. It was developed for its ability to inhibit calcium ion influx into vascular smooth muscle and myocardial cells, leading to vasodilation and reduced blood pressure. Nifedipine was introduced into clinical use in the 1970s and has since become an important medication in the treatment of hypertension and angina pectoris.

As a calcium channel blocker, nifedipine selectively targets L-type calcium channels, preventing calcium-dependent contraction of vascular smooth muscle. This action results in arterial vasodilation, reducing peripheral resistance and lowering blood pressure. Additionally, nifedipine's ability to relax coronary arteries improves oxygen supply to the heart, making it effective in the management of angina. The drug is classified into immediate-release and extended-release formulations, with the latter designed to maintain stable plasma concentrations and minimize fluctuations in blood pressure.

Nifedipine is widely prescribed for the treatment of hypertension, particularly in patients who require long-term blood pressure management. It is also used for the treatment and prevention of chronic stable angina and variant angina, conditions characterized by reduced coronary blood flow. In some cases, nifedipine has been employed in obstetrics to manage preterm labor due to its smooth muscle relaxant properties. However, its use in this context is subject to specific clinical guidelines.

The pharmacokinetics of nifedipine include rapid absorption following oral administration, with metabolism occurring primarily in the liver through the cytochrome P450 system. The drug's elimination is predominantly renal, with inactive metabolites excreted in the urine. Due to its pharmacological profile, interactions with other medications that affect liver enzymes, such as certain antifungals and anticonvulsants, can influence its efficacy and safety.

Nifedipine remains a key medication in cardiovascular therapy, with continued research focusing on its long-term effects and potential new applications. Advances in formulation technology have contributed to improved drug delivery, ensuring sustained efficacy with reduced side effects.

References

2025. [Elevated blood pressure and hypertension : Focus of the 2024 ESC guidelines on risk reduction]. Herz, 50(1).
DOI: 10.1007/s00059-024-05285-8

2025. Live-Cell Calcium Imaging in 3D Intestinal Organoids. Methods in molecular biology (Clifton, N.J.), 2792.
DOI: 10.1007/978-1-0716-4164-4_16

2024. Severe influenza A viral pneumonia in a hemodialysis patient: successful treatment with steroid pulse therapy. CEN Case Reports, 13(6).
DOI: 10.1007/s13730-024-00951-6
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