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bPiDDB
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Catalog No. T37818Cas No. 525596-66-1
Alias N,N'-Dodecylbis-Picolinium Bromide
bPiDDB (N,N'-Dodecylbis-Picolinium Bromide) is a nicotinic receptor (nAChR) antagonist.
bPiDDB
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Purity: 99.71%
Catalog No. T37818Alias N,N'-Dodecylbis-Picolinium BromideCas No. 525596-66-1
bPiDDB (N,N'-Dodecylbis-Picolinium Bromide) is a nicotinic receptor (nAChR) antagonist.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | $33 | In Stock | In Stock | |
| 10 mg | $58 | In Stock | In Stock | |
| 25 mg | $119 | In Stock | In Stock | |
| 50 mg | $175 | In Stock | In Stock | |
| 100 mg | $260 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $40 | In Stock | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.71%
Appearance:Solid
Color:White
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Product Introduction
bPiDDB AI Summary
bPiDDB exhibits antagonist activity at nicotinic acetylcholine receptors (nAChR) in rat striatal slices, showing potent inhibition of nicotine-evoked [3H]dopamine release with an IC50 value of 2.0 nM. It demonstrates high affinity for the alpha4-beta2 subtype of nAChR, with a Ki value of 48600.0 nM, while showing considerably lower affinity for the alpha7 subtype, requiring concentrations greater than 100000.0 nM to displace ligands. In addition, bPiDDB inhibits nicotine-evoked [3H]dopamine overflow by up to 78.0% at a concentration of 100 uM and exhibits binding activity to the blood-brain barrier choline transporter with a Ki value of 36000.0 nM. These properties suggest its potential role in modulating cholinergic neurotransmission and dopamine signaling..
Note: Summary generated by AI. Data source: ChEMBL 
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | bPiDDB (N,N'-Dodecylbis-Picolinium Bromide) is a nicotinic receptor (nAChR) antagonist. |
| Synonyms | N,N'-Dodecylbis-Picolinium Bromide |
| Molecular Weight | 514.38 |
| Formula | C24H38Br2N2 |
| Cas No. | 525596-66-1 |
| Smiles | [Br-].[Br-].Cc1ccc[n+](CCCCCCCCCCCC[n+]2cccc(C)c2)c1 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||
| Solubility Information | DMSO: 5.15 mg/mL (10.01 mM), Sonication is recommended.  | ||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||
DMSO
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Calculator
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
Tech Support
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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