Nicardipine (hydro<wbr>chloride)

Nicardipine (hydrochloride)

CAT N°: 17537
Price:

From 48.00 40.80

Nicardipine is a dihydropyridine L-type calcium channel antagonist that displays antihypertensive and antianginal activity.{28535} It is reported to inhibit adenosine A1, A2A, and A3 receptors with Ki values of 19.6, 63.8, and 3.25 µM, respectively, and can inhibit cytochrome P450 3A4 catalytic activity with an IC50 value of 0.148 µM.{28536,27561} Additionally, nicardipine has been shown to activate transient receptor potential A1 channels, producing an increase in Ca2+ (EC50 = 0.5 µM).{23938}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid, 3-methyl 5-[2-[methyl(phenylmethyl)amino]ethyl] ester, monohydrochloride
  • Correlated keywords
    • 55985-32-5 76093-35-1 76093-36-2 152046-25-8 L-type calcium channel blocker antagonist Ca2+ hypertension angina cardiology dihydropyridine adenosine A3 receptor inhibitor cytochrome P450 CYP3A4 TRPA1 biochemical ion pump inhibit intracellular signaling Lecibral Nicapress Barizin Bionicard Cardene Cardepine Dacarel Lescodil Nerdipina Nicant Loxen RS 69216XX07-0 RS69216XX07-0 RS69216 YC 93 YC93 Nicardal Nicarpin Nicodel Nimicor Perdipina Perdipine Ranvil Ridene Rycarden Rydene Vasodin Vasonase dihydropyridine antihypertension antihypertensive antianginal A1 A2A transient receptor potential TRP
  • Product Overview:
    Nicardipine is a dihydropyridine L-type calcium channel antagonist that displays antihypertensive and antianginal activity.{28535} It is reported to inhibit adenosine A1, A2A, and A3 receptors with Ki values of 19.6, 63.8, and 3.25 µM, respectively, and can inhibit cytochrome P450 3A4 catalytic activity with an IC50 value of 0.148 µM.{28536,27561} Additionally, nicardipine has been shown to activate transient receptor potential A1 channels, producing an increase in Ca2+ (EC50 = 0.5 µM).{23938}

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