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ChemicalBook--->CAS DataBase List--->86189-69-7

86189-69-7

86189-69-7 Structure

86189-69-7 Structure
IdentificationMore
[Name]

Felodipine
[CAS]

86189-69-7
[Synonyms]

4-(2,3-DICHLOROPHENYL)-1,4-DIHYDRO-2,6-DIMETHYL-3,5-PYRIDINECARBOXYLIC ACID ETHYL METHYL ESTER
4-(2,3-DICHLOROPHENYL)-1,4-DIHYDRO-2,6-DIMETHYL-3,5-PYRIDINECARBOXYLIC ACID METHYL ESTER
4-(2,3-DICHLOROPHENYL)-1,4-DIHYDRO-2,6-DIMETHYL-3,5-PYRIDINEDICARBOXYLIC ACID METHYL ESTER
ethyl methyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
FELODAY
FELODIPINE
FLODIL
PLENDIL
Felodipine
[Molecular Formula]

C18H19Cl2NO4
[MDL Number]

MFCD00868316
[Molecular Weight]

384.25
[MOL File]

86189-69-7.mol
Chemical PropertiesBack Directory
[solubility ]

DMSO: 28 mg/mL
[form ]

solid
[color ]

light yellow
[CAS DataBase Reference]

86189-69-7(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
[WGK Germany ]

3
[RTECS ]

US7968700
Hazard InformationBack Directory
[Uses]

Vasodilator.
[Brand name]

Plendil (AstraZeneca).
[Clinical Use]

Calcium-channel blocker:
Hypertension
Angina
[Drug interactions]

Potentially hazardous interactions with other drugs
Aminophylline and theophylline: possibly increased aminophylline and theophylline concentration.
Anaesthetics: enhanced hypotensive effect.
Antibacterials metabolism possibly inhibited by clarithromycin, erythromycin and telithromycin.
Antidepressants: enhanced hypotensive effect with MAOIs.
Antiepileptics: effect reduced by carbamazepine, barbiturates, phenytoin and primidone.
Antifungals: metabolism inhibited by itraconazole and ketoconazole; negative inotropic effect possibly increased with itraconazole.
Antihypertensives: enhanced hypotensive effect, increased risk of first dose hypotensive effect of postsynaptic alpha-blockers.
Antivirals: concentration possibly increased by ritonavir; use with caution with telaprevir.
Grapefruit juice: concentration increased - avoid concomitant use.
Tacrolimus: possibly increased tacrolimus concentration
[Metabolism]

Felodipine is metabolised in the liver and all identified metabolites are devoid of vasodilating properties. Approximately 70% of a given dose is excreted as metabolites in the urine and about 10% with the faeces. Less than 0.5% of the dose is excreted unchanged in the urin
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