Clevidipine

CAT:
804-HY-17436-01
Size:
5 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Clevidipine - image 1

Clevidipine

  • Description:

    Clevidipine is a selective, short-acting L-type calcium channel antagonist with an IC50 of 7.1 nM. Clevidipine can competitively bind to calcium channels and exert rapid vasoselective vasodilation by blocking the influx of extracellular calcium ions, thereby reducing peripheral vascular resistance and effectively controlling acute severe hypertension. Clevidipine can also protect the myocardium from reperfusion injury by promoting the release of nitric oxide (NO) . Clevidipine can be used in the research of acute hypertension, perioperative blood pressure management, and myocardial ischemia-reperfusion injury[1].
  • UNSPSC:

    12352005
  • Hazard Statement:

    H301, H361
  • Target:

    Calcium Channel
  • Type:

    Reference compound
  • Related Pathways:

    Membrane Transporter/Ion Channel; Neuronal Signaling
  • Applications:

    COVID-19-immunoregulation
  • Field of Research:

    Cardiovascular Disease; Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/Clevidipine.html
  • Purity:

    99.85
  • Solubility:

    DMSO : ≥ 50 mg/mL
  • Smiles:

    O=C(C1=C(C)NC(C)=C(C(OCOC(CCC)=O)=O)C1C2=CC=CC(Cl)=C2Cl)OC
  • Molecular Formula:

    C21H23Cl2NO6
  • Molecular Weight:

    456.32
  • Precautions:

    H301, H361
  • References & Citations:

    [1]Pollack CV, et al. Clevidipine, an intravenous dihydropyridine calcium channel blocker, is safe and effective for the treatment of patients with acute severe hypertension. Ann Emerg Med. 2009 Mar;53 (3) :329-38.|[2]Gourine A, et al. Short-acting calcium antagonist clevidipine protects against reperfusion injury via local nitric oxide-related mechanisms in the jeopardised myocardium. Cardiovasc Res. 2001 Jul;51 (1) :100-7.|[3]Wang Y, et al. Pharmacokinetics and tissue distribution study of clevidipine and its primary metabolite H152/81 in rats. Biomed Chromatogr. 2018 Feb;32 (2) .|[4]Wiśniowska B, et al. Predictive model for L-type channel inhibition: multichannel block in QT prolongation risk assessment. J Appl Toxicol. 2012 Oct;32 (10) :858-66.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    4°C (Powder, protect from light)
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    Launched
  • CAS Number:

    [167221-71-8]