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nAChR antagonist 2
Catalog No. T215124 Copy Product Info
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nAChRantagonist 2 is a selective nAChR antagonist that demonstrates inhibitory activity against nAChR subtypes, including human α9α10, α9, and α7, in Xenopus laevis oocytes, with IC50 values of 16.0 nM, 26.2 nM, and 336.3 nM, respectively. It inhibits ATP-induced IL-1β release at nanomolar concentrations and can be utilized in research related to non-opioid analgesics and immunomodulators.
nAChR antagonist 2
Copy Product Info🥰Excellent
Catalog No. T215124
nAChRantagonist 2 is a selective nAChR antagonist that demonstrates inhibitory activity against nAChR subtypes, including human α9α10, α9, and α7, in Xenopus laevis oocytes, with IC50 values of 16.0 nM, 26.2 nM, and 336.3 nM, respectively. It inhibits ATP-induced IL-1β release at nanomolar concentrations and can be utilized in research related to non-opioid analgesics and immunomodulators.
nAChR antagonist 2
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | nAChRantagonist 2 is a selective nAChR antagonist that demonstrates inhibitory activity against nAChR subtypes, including human α9α10, α9, and α7, in Xenopus laevis oocytes, with IC50 values of 16.0 nM, 26.2 nM, and 336.3 nM, respectively. It inhibits ATP-induced IL-1β release at nanomolar concentrations and can be utilized in research related to non-opioid analgesics and immunomodulators. |
| In vitro | nAChR antagonist 2 (compound 22) effectively inhibits acetylcholine-induced currents mediated by α9 subunit-containing nAChRs expressed in Xenopus laevis oocytes, with IC50 values for hα9α10, hα9, and hα7 receptors at 16.0 nM, 26.2 nM, and 336.3 nM, respectively. Additionally, at concentrations of 100 pM or 100 nM for 40 minutes, it exhibits both antagonistic and agonistic effects on neuronal nicotinic receptors in THP-1 monocytes. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
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In Vivo Formulation Calculator (Clear solution)
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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.Stock Solution Preparation:
Dissolve 2 mg of the compound in 100 μL DMSO to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
Preparation of the In Vivo Formulation:
1) Add 100 μL of the DMSO stock solution to 400 μL PEG300 and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O and mix thoroughly until a homogeneous solution is obtained.
This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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