Nicardipine hydrochloride
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Nicardipine hydrochloride
structure -
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CAS No:
54527-84-3
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Formula:
C26H29N3O6.ClH
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Chemical Name:
Nicardipine hydrochloride
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Synonyms:
3,5-Pyridinedicarboxylic acid,1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-,3-methyl 5-[2-[methyl(phenylmethyl)amino]ethyl] ester,hydrochloride (1:1);3,5-Pyridinedicarboxylic acid,1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-,methyl 2-[methyl(phenylmethyl)amino]ethyl ester,monohydrochloride;2,6-Dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3-[2-(N-benzyl-N-methylamino)]-ethyl ester 5-methyl ester hydrochloride;YC 93;Nicardipine hydrochloride;Perdipine;Cardene;Cardene (pharmaceutical);Vasonase;Ridene;Vasodin;Nicardal;Nicapress;Lescodil;RS 69216;Rycarden;Nerdipina;Lecibral;Nicant;RS 69216XX07-0;Bionicard;Dacarel;Barizin;Nicodel;Perdipina;Ranvil;Loxen;Nimicor;Rydene;Nicarpin;Cardepine;Cardene SR;152046-25-8
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Categories:
Active Pharmaceutical Ingredients > Circulatory System Drugs
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CAS No:
Description
Nicardipine Hcl(YC-93) is a calcium channel blocker that has been widely used to control blood pressure in severe hypertension following events such as ischemic stroke, traumatic brain injury, and intracerebral hemorrhage.
Characteristics
114
5.33180
yellow powder
168-170 °C
603.4°C at 760 mmHg
318.7ºC
DMSO: ~1 mg/mL
2-8°C
LD50 in male, female rats (mg/kg): 634, 557 orally; 18.1, 25.0 i.v.; in male, female mice: 634, 650 orally; 20.7, 19.9 i.v. (Odani, Sado)
Safety Information
Ⅲ
6.1(b)
UN 2811 6.1/PG 3
3
23/24/25
36/37/39-45
US7972100
T
P261-P280-P301 + P310-P311
H301-H311-H331
Nicardipine hydrochloride Use and Manufacturing
Nicardipine is a dihydropyridine L-type calcium channel antagonist that displays antihypertensive and antianginal activity. 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. Additionally, nicardipine has been shown to activate transient receptor potential A1 channels, producing an increase in Ca2+ (EC50 = 0.5 μM).
Drug Function and Efficacy
It inhibits the transmembrane calcium ion influx between the myocardium and vascular smooth muscle without changing the blood calcium concentration, selectively dilates the coronary vascular smooth muscle, reduces peripheral vascular resistance, reduces myocardial oxygen consumption and total peripheral resistance, and increases coronary collateral circulation and coronary blood flow.
Registered Holders
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WOCKHARDT LTD
Active
Brazil
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LUSOCHIMICA SPA
Active
Brazil
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OLON S.P.A.
Active
Italy
Recommended Suppliers of Nicardipine hydrochloride
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