
Nicardipine
CAS No. 55985-32-5
Nicardipine( YC-93 )
Catalog No. M15039 CAS No. 55985-32-5
Nicardipine(YC-93) is a calcium channel blocker that has been widely used to control blood pressure in severe hypertension.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 45 | Get Quote |
![]() ![]() |
10MG | 65 | Get Quote |
![]() ![]() |
25MG | 91 | Get Quote |
![]() ![]() |
50MG | 138 | Get Quote |
![]() ![]() |
100MG | 206 | Get Quote |
![]() ![]() |
200MG | Get Quote | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameNicardipine
-
NoteResearch use only, not for human use.
-
Brief DescriptionNicardipine(YC-93) is a calcium channel blocker that has been widely used to control blood pressure in severe hypertension.
-
DescriptionNicardipine(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.Hypertension Phase 3 Clinical.
-
In VitroNicardipine (0.1-10 μM; 24-48 h) reduces viability and proliferation of vascular smooth muscle cells (VSMCs) and inhibits their ability to migrate. Cell Viability Assay Cell Line:VSMCs were isolated from New Zealand rabbit aortic preparations Concentration:0.1 μM, 1 μM, 3 μM, 10 μM Incubation Time:24-48 hours Result:Treatment reduced significantly cell viability and inhibited VSMCs proliferation in the presence of 10% FBS in a dose-dependent way, from 205.4±17.5% to 176.6±17%, 160.6±5.7%, 150.4±11.2%, 61.22±7.83% after 0.1 μM, 1 μM, 3 μM, 10 μM treatment, respectively.
-
In VivoNicardipine (0.3-10 mg/kg; p.o.) shows antihypertensive properties. LD50s of Nicardipine are 643 mg/kg (oral) and 557 mg/kg (oral); 18.1 mg/kg (intravenous) 25.0 mg/kg (intravenous); 735 mg/kg (subcutaneous) and 683 mg/kg (subcutaneous); 171 mg/kg (intraperitoneally) and 155 mg/kg (intraperitoneally) for male and female Sprague-Dawley rats, respectively. LD50s of Nicardipine are 187 mg/kg (oral) and 15.5 mg/kg (intravenous) for male Wistar rats, respectively. LD50s of Nicardipine are 634 mg/kg (oral) and 650 mg/kg (oral); 20.7 mg/kg (intravenous) 19.9 mg/kg (intravenous); 540 mg/kg (subcutaneous) and 710 mg/kg (subcutaneous); 144mg/kg (intraperitoneally) and 161 mg/kg (intraperitoneally) for male and female mice, respectively. Animal Model:In conscious normotensive rats (NR)Dosage:0.3-10 mg/kg Administration:P.o.Result:Induced a dose-dependent hypotensive response (maximal decrease in mean blood pressure, supine position) without any postural hypotensive response.
-
SynonymsYC-93
-
PathwayGPCR/G Protein
-
TargetCalcium Channel
-
RecptorCalcium Channel
-
Research AreaCardiovascular Disease
-
IndicationHypertension
Chemical Information
-
CAS Number55985-32-5
-
Formula Weight479.525
-
Molecular FormulaC26H29N3O6
-
Purity>98% (HPLC)
-
Solubility10 mM in DMSO
-
SMILESCC1=C(C(OC)=O)C(C2=CC([N+]([O-])=O)=CC=C2)C(C(OCCN(CC3=CC=CC=C3)C)=O)=C(C)N1
-
Chemical Name3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-, 3-methyl 5-[2-[methyl(phenylmethyl)amino]ethyl] ester
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Huang BR, et al. PLoS One. 2014 Mar 12;9(3):e91167.
2. Amenta F, et al. J Hypertens Suppl. 1996 Oct;14(3):S29-35.
3. Gasior M, et al. J Neural Transm. 1996;103(7):819-31.
molnova catalog



related products
-
Lacidipine
Lacidipine (Lacipil, Motens) is a L-type calcium channel blocker.
-
Strophanthidin
Strophanthidin can induce calcium overload in vivo.
-
Ginsenoside-Rf
Ginsenoside Rf is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel.