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CARVEDILOL-D5

Base Information Edit
  • Chemical Name:CARVEDILOL-D5
  • CAS No.:929106-58-1
  • Molecular Formula:C24H21D5N2O4
  • Molecular Weight:411.51
  • Hs Code.:
  • Mol file:929106-58-1.mol
CARVEDILOL-D5

Synonyms:CARVEDILOL-D5

Suppliers and Price of CARVEDILOL-D5
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Carvedilol-d5
  • 1mg
  • $ 460.00
  • TRC
  • Carvedilol-d5
  • 10mg
  • $ 1455.00
  • Cayman Chemical
  • Carvedilol-d5 ≥99% deuterated forms (d1-d5)
  • 1mg
  • $ 163.00
  • Cayman Chemical
  • Carvedilol-d5 ≥99% deuterated forms (d1-d5)
  • 500μg
  • $ 136.00
  • American Custom Chemicals Corporation
  • CARVEDILOL-D5 95.00%
  • 5MG
  • $ 495.59
  • AK Scientific
  • Carvedilol-d5
  • 1mg
  • $ 302.00
Total 4 raw suppliers
Chemical Property of CARVEDILOL-D5 Edit
Chemical Property:
  • PSA:75.74000 
  • LogP:4.12890 
Purity/Quality:

99% *data from raw suppliers

Carvedilol-d5 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Description Carvedilol-d5 is intended for use as an internal standard for the quantification of carvedilol by GC- or LC-MS. Carvedilol is a non-selective antagonist of the β-adrenergic receptor (β-AR; Kds = 1.78, 0.4, and 5.01 nM for β1-, β2-, and β3-ARs, respectively). It also binds to α1-, but not α2-, adrenergic receptors (Kis = 0.81 and 3,400 nM, respectively). Carvedilol reverses increases in heart rate induced by the β1-AR agonist isoproterenol in isolated guinea pig atria (Kb = 0.8 nM) and induces relaxation of isolated precontracted guinea pig trachea (Kb = 1.3 nM). It prevents epinephrine-induced premature ventricular beats in a rat model of arrhythmia with an ED50 value of 0.25 mg/kg. Carvedilol also inhibits the contractile response to the α1-AR agonist norepinephrine in isolated rabbit aorta (Kb = 11 nM). It decreases systolic blood pressure and heart rate in rat models of hypertension, including spontaneously hypertensive, renal hypertensive, and deoxycorticosterone acetate-treated rats when administered at doses ranging from 3 to 30 mg/kg. Carvedilol also activates cardioprotective signaling through β-arrestin and ERK1/2 activation. Formulations containing carvedilol have been used in the treatment of congestive heart failure and hypertension.
  • Uses Carvedilol-d5 is the labelled analog of Carvedilol, a nonselective β-adrenergic blocker with α1-blocking activity. Carvedilol is an antihypertensive used in the treatment of congestive heart failure. Labeled Carvedilol, intended for use as an internal standard for the quantification of Carvedilol by GC- or LC-mass spectrometry.
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