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Varenicline-d4 hydrochloride

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Catalog No. TMID-0733

Varenicline-d4hydrochloride is a deuterium-labeled form of Varenicline (dihydrochloride). Varenicline (CP 526555) dihydrochloride acts as a partial agonist for the α4β2 nicotinic acetylcholine receptor (α4β2nAChR), with an EC50 of 2.3 μM. It serves as a full agonist for α3β4nAChR and α7nAChR, with EC50 values of 55 μM and 18 μM, respectively. As a nicotine ligand based on a cytosine structure, Varenicline dihydrochloride is utilized in smoking cessation research.

Varenicline-d4 hydrochloride
Other Forms of Varenicline-d4 hydrochloride:

Varenicline-d4 hydrochloride

😃Good
Catalog No. TMID-0733
Varenicline-d4hydrochloride is a deuterium-labeled form of Varenicline (dihydrochloride). Varenicline (CP 526555) dihydrochloride acts as a partial agonist for the α4β2 nicotinic acetylcholine receptor (α4β2nAChR), with an EC50 of 2.3 μM. It serves as a full agonist for α3β4nAChR and α7nAChR, with EC50 values of 55 μM and 18 μM, respectively. As a nicotine ligand based on a cytosine structure, Varenicline dihydrochloride is utilized in smoking cessation research.
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Product Introduction

Bioactivity
Description
Varenicline-d4hydrochloride is a deuterium-labeled form of Varenicline (dihydrochloride). Varenicline (CP 526555) dihydrochloride acts as a partial agonist for the α4β2 nicotinic acetylcholine receptor (α4β2nAChR), with an EC50 of 2.3 μM. It serves as a full agonist for α3β4nAChR and α7nAChR, with EC50 values of 55 μM and 18 μM, respectively. As a nicotine ligand based on a cytosine structure, Varenicline dihydrochloride is utilized in smoking cessation research.
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Stock solution preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (stock solution concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
The above example illustrates how to use "In Vivo Formulation Calculator" and does not represent a recommended formulation for any specific compound. Please select an appropriate dissolution method based on your experimental animals and route of administration.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
1 Enter information below:
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2 Enter the in vivo formulation:
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