Nisoldipine
Systematic (IUPAC) name | |
---|---|
isobutyl methyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate | |
Clinical data | |
Trade names | Sular |
AHFS/Drugs.com | monograph |
MedlinePlus | a696009 |
Pregnancy category |
|
Legal status |
|
Routes of administration | Oral |
Pharmacokinetic data | |
Protein binding | 99% |
Biological half-life | 7-12 hours |
Identifiers | |
CAS Number | 63675-72-9 |
ATC code | C08CA07 |
PubChem | CID 4499 |
IUPHAR/BPS | 2524 |
DrugBank | DB00401 |
ChemSpider | 4343 |
UNII | 4I8HAB65SZ |
KEGG | D00618 |
ChEBI | CHEBI:7577 |
ChEMBL | CHEMBL1726 |
Chemical data | |
Formula | C20H24N2O6 |
Molar mass | 388.414 g/mol |
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Nisoldipine (INN) is a calcium channel blocker of the dihydropyridine class. It sold in the United States under the proprietary name Sular. Nisoldipine has tropism for cardiac blood vessels.[1]
External links
- Mielcarek J, Grobelny P, Szamburska O (2005). "The effect of beta-carotene on the photostability of nisoldipine.". Methods Find Exp Clin Pharmacol 27 (3): 167–71. doi:10.1358/mf.2005.27.3.890873. PMID 15834448.
- Missan S, Zhabyeyev P, Dyachok O, Jones SE, McDonald TF (November 2003). "Block of cardiac delayed-rectifier and inward-rectifier K+ currents by nisoldipine". Br. J. Pharmacol. 140 (5): 863–70. doi:10.1038/sj.bjp.0705518. PMC 1574108. PMID 14530219.
- Hamilton S, Houle L, Thadani U (1999). "Rapid-release and coat-core formulations of nisoldipine in treatment of hypertension, angina, and heart failure.". Heart Dis 1 (5): 279–88. PMID 11720635.
References
- ↑ "Why is nisoldipine a specific agent in ischemic left ventricular dysfunction?". The American Journal of Cardiology 75: E36–E40. doi:10.1016/S0002-9149(99)80446-9.
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