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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
10MG 29 In Stock
25MG 50 In Stock
50MG 75 In Stock
100MG 124 In Stock
200MG 223 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock
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Biological Information

  • Product Name
    Clevidipine
  • Note
    Research use only, not for human use.
  • Brief Description
    A dihydropyridine L-type calcium channel blocker, highly selective for vascular and has little or no effect on myocardial contractility or cardiac conduction.
  • Description
    A 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.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Clevidipine | Clevidipine butyrate | Cleviprex | 167221-71-8 | Clevelox | Rac-Clevidipine
  • Pathway
    GPCR/G Protein
  • Target
    Calcium Channel
  • Recptor
    AChR|CalciumChannel
  • Research Area
    Cardiovascular Disease
  • Indication
    Hypertension

Chemical Information

  • CAS Number
    167221-71-8
  • Formula Weight
    456.3164
  • Molecular Formula
    C21H23Cl2NO6
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    CCCC(=O)OCOC(=O)C1=C(NC(=C(C1C2=C(C(=CC=C2)Cl)Cl)C(=O)OC)C)C
  • Chemical Name
    3,5-Pyridinedicarboxylic acid,4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-, 3-methyl 5-[(1-oxobutoxy)methyl] ester

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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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