ChemicalBook--->CAS DataBase List--->132866-11-6

132866-11-6

132866-11-6 Structure

132866-11-6 Structure
IdentificationMore
[Name]

Lercanidipine hydrochloride
[CAS]

132866-11-6
[Synonyms]

75
CLAP
mE10
c-E10
CIPER
BCL10
CarMen
LerzaM
Zandip
Lercan
Zanicor
Corifeo
Renovia
Vasodip
Lercadip
Lercapin
Lercaton
LerkaMen
Cardiovasc
BCL-10 human
Lercaridipine
LERCANIDIPINE HCL
B-cell CLL/lymphoma 10
B-cell lymphoma/leukemia 10
LERCANIDIPINE HYDROCHLORIDE
LERCANIDIPINEHYDROCHLORIDE(FORR&DONLY)
Lercanidipine hydrochloride heMihydrate
CARD-containing molecule enhancing NF-κ-B
Lercanidipine hemihydrate hydrochloride
1,4-dihydro-2,6-diMethyl-4-(3-nitrophenyl)-3,5-
1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylicAcid2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimeth
1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)methylamino]-1,1-dimethylethyl methyl ester hydrochloride
1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-[(3,3-diphenylpropyl)methylamino]-1,1-dimethylethyl methyl ester hydrochloride
1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-2-[(3,3-diphenylpropyl)methylamino]-1,1-dimethylethyl methyl ester 3,5-pyridinedicarboxylic acid hydrochloride
O3-[1-[3,3-diphenylpropyl(methyl)amino]-2-methyl-propan-2-yl] O5-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate hydrochloride
1,4-Dihydro-2,6-dimethyl-4-(3-nittrophenyl)-3,5-pyridinedicarboxylic Acid 2-[(3,3-Diphenylpropyl)methylamino]-1,1-dimethylethyl Methyl Ester Hydrochloride
3-O-[1-[3,3-diphenylpropyl(methyl)amino]-2-methylpropan-2-yl] 5-O-methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate hydrochloride
3,5-Pyridinedicarboxylicacid, 1,4-dihydro-2,6-diMethyl-4-(3-nitrophenyl)-,3-[2-[(3,3-diphenylpropyl)MethylaMino]-1,1-diMethylethyl] 5-Methyl ester,hydrochloride (1:1)
2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid O3-[2-[3,3-diphenylpropyl(methyl)amino]-1,1-dimethyl-ethyl] ester O5-methyl ester hydrochloride
[EINECS(EC#)]

603-682-3
[Molecular Formula]

C36H42ClN3O6
[MDL Number]

MFCD07773089
[Molecular Weight]

648.19
[MOL File]

132866-11-6.mol
Chemical PropertiesBack Directory
[Appearance]

Pale-Yellow Powder
[Melting point ]

175-177°C
[storage temp. ]

2-8°C
[solubility ]

soluble in Methanol
[form ]

powder
[color ]

yellow
[Usage]

A dihydropyridine calcium channel blocker
[Merck ]

14,5446
[InChIKey]

WMFYOYKPJLRMJI-UHFFFAOYSA-N
[CAS DataBase Reference]

132866-11-6(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

R25:Toxic if swallowed.
[Safety Statements ]

S36/37:Wear suitable protective clothing and gloves .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

UN 2811
[WGK Germany ]

3
[HS Code ]

2933.39.4100
[Toxicity]

LD50 in mice (mg/kg): 83 i.p.; 657 orally (Nardi)
Hazard InformationBack Directory
[Chemical Properties]

Pale-Yellow Powder
[Uses]

A dihydropyridine calcium channel blocker. Antihypertensive.
[Uses]

long-acting dihydropyridine calcium channel blocker, antihypertensive
[Definition]

ChEBI:Lercanidipine hydrochloride is a diarylmethane.
[Brand name]

Cardiovasc (Recor dati, Italy); Carmen (Recordati, Italy); Corifeo (Recordati, Italy); Lercadip (Recordati, Italy); Lercan (Recordati, Italy); Lercapin (Recordati, Italy); Lercaton (Recordati, Italy); Lerkamen (Recordati, Italy); Lerzam (Recordati, Italy); Renovia (Recordati, Italy); Vasodip (Recordati, Italy); Zandip (Recordati, Italy); Zanicor (Recordati, Italy).
[Biological Activity]

L-type Ca 2+ channel blocker that displays higher vascular selectivity than Felodipine (4-(2,3-Dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid ethyl methyl ester ). Causes peripheral vasodilation with only weak negative inotropic activity. Antihypertensive.
[Biochem/physiol Actions]

Lercanidipine hydrochloride is a L-type (Cav1.2b) vascular channel antagonist; L-type (Cav1.2a) cardiac channel agonist voltage-dependent and highly lipophylic compound, which exhibits a slower onset and longer duration of action than other calcium channel antagonists; an antihypertensive agent in patients with mild-to-moderate hypertension; more vasoselective than lacidipine and amlodipine.
[Clinical Use]

#N/A
[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 - avoid with erythromycin. Antidepressants: enhanced hypotensive effect with MAOIs. Antiepileptics: effect reduced by carbamazepine, barbiturates, phenytoin and primidone. Antifungals: metabolism possibly inhibited by itraconazole and ketoconazole - avoid; negative inotropic effect possibly increased with itraconazole. Antihypertensives: enhanced hypotensive effect, increased risk of first dose hypotensive effect of postsynaptic alpha-blockers. Antivirals: concentration increased by ritonavir - avoid. Cardiac glycosides: digoxin concentration increased. Ciclosporin: concentration of both drugs may be increased - avoid. Grapefruit juice: concentration increased - avoid
[storage]

Store at -20°C
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

132866-11-6(sigmaaldrich)
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