Product
Supplier
Encyclopedia
Inquiry
Home > Encyclopedia > Nicardipine hydrochloride

Nicardipine hydrochloride

pharmaceutical raw materials
Nicardipine hydrochloride structure

Nicardipine hydrochloride 

structure
  • CAS No:

    54527-84-3

  • Formula:

    C26H29N3O6.ClH

  • Chemical Name:

    Nicardipine hydrochloride

  • 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

  • Categories:

    Active Pharmaceutical Ingredients  >  Circulatory System Drugs

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.

Nicardipine hydrochloride Basic Attributes

515.99

515.182312

259-198-4

2933399090

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

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.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • WOCKHARDT LTD

    Brazil Brazil
    Active
  • LUSOCHIMICA SPA

    Brazil Brazil
    Active
  • OLON S.P.A.

    Italy Italy
    Active

Recommended Suppliers of Nicardipine hydrochloride

Scan the QR Code to Share

Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.