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NGB 2904

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Catalog No. T28167Cas No. 189060-98-8
Alias NGB-2904, NGB2904

NGB 2904 is a potent and selective antagonist of dopamine D3 receptor (Ki values are 1.4, 217, 223, 642, > 5000, > 10000 and > 10000 nM for D3, D2, 5-HT2, α1, D4, D1 and D5 receptors respectively). NGB2904 potently antagonizes mitogenesis stimulated by quinpirole (IC50 = 6.8 nM).

NGB 2904

NGB 2904

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Purity: 98.79%
Catalog No. T28167Alias NGB-2904, NGB2904Cas No. 189060-98-8
NGB 2904 is a potent and selective antagonist of dopamine D3 receptor (Ki values are 1.4, 217, 223, 642, > 5000, > 10000 and > 10000 nM for D3, D2, 5-HT2, α1, D4, D1 and D5 receptors respectively). NGB2904 potently antagonizes mitogenesis stimulated by quinpirole (IC50 = 6.8 nM).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
2 mg$34In StockIn Stock
5 mg$53In StockIn Stock
10 mg$83In StockIn Stock
25 mg$166In StockIn Stock
50 mg$294In StockIn Stock
100 mg$415In StockIn Stock
500 mgPreferential-In Stock
1 mL x 10 mM (in DMSO)$69In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.79%
Appearance:Solid
Color:White
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Product Introduction

NGB 2904 AI Summary
NGB 2904 has a high selectivity ratio for the human dopamine D3 receptor over the human dopamine D2 receptor, with a selectivity ratio greater than 200.0, suggesting potential bioactivity in selectively targeting the dopamine D3 receptor. Additionally, the compound exhibits antiviral activity against SARS-CoV-2. It inhibits the cytotoxicity of Caco-2 cells with a -7.86% inhibition at a concentration of 10 µM after 48 hours. In VERO-6 cells, NGB 2904 demonstrates an inhibition of -0.02% under similar conditions. Furthermore, it inhibits the SARS-CoV-2 3CL-Pro protease with an inhibition rate of -2.66% at 20 µM, indicating its potential to interfere with viral replication and pathogenesis..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
NGB 2904 is a potent and selective antagonist of dopamine D3 receptor (Ki values are 1.4, 217, 223, 642, > 5000, > 10000 and > 10000 nM for D3, D2, 5-HT2, α1, D4, D1 and D5 receptors respectively). NGB2904 potently antagonizes mitogenesis stimulated by quinpirole (IC50 = 6.8 nM).
Targets&IC50
α1-adrenoceptor:642 nM(Ki), D4:> 5000 nM(Ki), 5-HT2:223 nM(Ki), D5:> 10000 nM(Ki), D1:> 10000 nM(Ki), D3:1.4 nM(Ki), D2:217 nM(Ki)
SynonymsNGB-2904, NGB2904
Chemical Properties
Molecular Weight494.46
FormulaC28H29Cl2N3O
Cas No.189060-98-8
SmilesClc1cccc(N2CCN(CCCCNC(=O)c3ccc-4c(Cc5ccccc-45)c3)CC2)c1Cl
Relative Density.1.264 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 16.25 mg/mL (32.86 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.0224 mL10.1120 mL20.2241 mL101.1204 mL
5 mM0.4045 mL2.0224 mL4.0448 mL20.2241 mL
10 mM0.2022 mL1.0112 mL2.0224 mL10.1120 mL
20 mM0.1011 mL0.5056 mL1.0112 mL5.0560 mL

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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:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 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 DMSOTargetMol | reagent 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 DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent 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.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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