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Clevidipine
CAS No. 167221-71-8
Clevidipine( Clevidipine | Clevidipine butyrate | Cleviprex | 167221-71-8 | Clevelox | Rac-Clevidipine )
Catalog No. M12548 CAS No. 167221-71-8
A dihydropyridine L-type calcium channel blocker, highly selective for vascular and has little or no effect on myocardial contractility or cardiac conduction.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 29 | In Stock |
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| 10MG | 29 | In Stock |
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| 25MG | 50 | In Stock |
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| 50MG | 75 | In Stock |
|
| 100MG | 124 | In Stock |
|
| 200MG | 223 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameClevidipine
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NoteResearch use only, not for human use.
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Brief DescriptionA dihydropyridine L-type calcium channel blocker, highly selective for vascular and has little or no effect on myocardial contractility or cardiac conduction.
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DescriptionA dihydropyridine L-type calcium channel blocker, highly selective for vascular and has little or no effect on myocardial contractility or cardiac conduction; reduces mean arterial blood pressure by decreasing systemic vascular resistance.Hypertension Approved.
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In Vitro——
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In Vivo——
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SynonymsClevidipine | Clevidipine butyrate | Cleviprex | 167221-71-8 | Clevelox | Rac-Clevidipine
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PathwayGPCR/G Protein
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TargetCalcium Channel
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RecptorAChR|CalciumChannel
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Research AreaCardiovascular Disease
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IndicationHypertension
Chemical Information
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CAS Number167221-71-8
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Formula Weight456.3164
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Molecular FormulaC21H23Cl2NO6
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESCCCC(=O)OCOC(=O)C1=C(NC(=C(C1C2=C(C(=CC=C2)Cl)Cl)C(=O)OC)C)C
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Chemical Name3,5-Pyridinedicarboxylic acid,4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-, 3-methyl 5-[(1-oxobutoxy)methyl] ester
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Schwieler JH, et al. J Cardiovasc Pharmacol. 1999 Aug;34(2):268-74.
2. Ericsson H, et al. Eur J Pharm Sci. 1999 Apr;8(1):29-37.
3. Huraux C, et al. Anesth Analg. 1997 Nov;85(5):1000-4.
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