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(Rac) -Nebivolol-d2,15N

(Rac) -Nebivolol-d2,15N is 15N and deuterated labeled (Rac) -Nebivolol. (Rac) -Nebivolol ((Rac) -R 065824) is a racemic isomer of Nebivolol. Nebivolol is a selective β1-adrenergic receptor antagonist with an IC50 value of 0.8 nM. Nebivolol can prevent up-regulation of Nox2/NADPH oxidase and lipoperoxidation in the early stages of ethanol-induced cardiac toxicity. Vasodilatory activity[1][2].

Product Specifications

Product Name Alternative

(Rac) -R 065824-d2,15N

UNSPSC

12352005

Target

Adrenergic Receptor; Isotope-Labeled Compounds; NADPH Oxidase

Type

Isotope-Labeled Compounds

Related Pathways

GPCR/G Protein; Metabolic Enzyme/Protease; Neuronal Signaling; Others

Applications

Neuroscience-Neuromodulation

Field of Research

Cardiovascular Disease

Solubility

10 mM in DMSO

Smiles

FC1=CC=C2OC(C(C[15NH]CC(C3OC4=CC=C(C=C4C([2H])C3)F)O)O)CC([2H])C2=C1

Molecular Formula

C22H23D2F2 15NO4

Molecular Weight

408.44

References & Citations

[1]do Vale GT, et al. Nebivolol Prevents Up-Regulation of Nox2/NADPH Oxidase and Lipoperoxidation in the Early Stages of Ethanol-Induced Cardiac Toxicity. Cardiovasc Toxicol. 2021 Mar;21 (3) :224-235.|[2]Cockcroft JR, et al. Nebivolol vasodilates human forearm vasculature: evidence for an L-arginine/NO-dependent mechanism. J Pharmacol Exp Ther. 1995 Sep;274 (3) :1067-71.|[3]Oelze M, et al. Nebivolol inhibits superoxide formation by NADPH oxidase and endothelial dysfunction in angiotensin II-treated rats. Hypertension. 2006 Oct;48 (4) :677-84.|[4]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53 (2) :211-216.

Shipping Conditions

Room temperature

Scientific Category

Isotope-Labeled Compounds

Clinical Information

No Development Reported

Frequently Asked Questions

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