Shopping Cart
Remove All
  • TargetMol
    Your shopping cart is currently empty

VU-29

Copy Product Info
😃Good
Catalog No. T23515Cas No. 890764-36-0
Alias VU 29

VU-29 is a positive allosteric mGlu5 receptor modulator with an EC50 of 9 nM and a Ki of 244 nM for rmGluR5. It is selective for mGluR5 relative to other mGluR subtypes [EC50: rmGluR1/rmGluR2=557 nM/1.5 μM; hmGluR4=154 nM].

VU-29

VU-29

Copy Product Info
😃Good
Purity: 99.63%
Catalog No. T23515Alias VU 29Cas No. 890764-36-0
VU-29 is a positive allosteric mGlu5 receptor modulator with an EC50 of 9 nM and a Ki of 244 nM for rmGluR5. It is selective for mGluR5 relative to other mGluR subtypes [EC50: rmGluR1/rmGluR2=557 nM/1.5 μM; hmGluR4=154 nM].
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
2 mg$29In StockIn Stock
5 mg$48In StockIn Stock
10 mg$83In StockIn Stock
25 mg$173In StockIn Stock
50 mg$287In StockIn Stock
100 mg$413In StockIn Stock
200 mg$589-In Stock
1 mL x 10 mM (in DMSO)$53In StockIn Stock
Add to Cart
Add to Quotation
In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Questions
TargetMol
View More

Batch Information

Select Batch
Purity:99.63%
Appearance:Solid
Color:White
Contact us for more batch information

Resource Download

Product Introduction

VU-29 AI Summary
VU-29 exhibits multiple bioactivities, showing significant interaction with mGluR5 and antiviral properties. It has a Ki of 250.0 nM in displacing [3H]methoxyPEPy from rat mGluR5 expressed in HEK293 cells and an EC50 of 10.7 nM in potentiating glutamate-induced calcium flux in rat astrocytes. In terms of antiviral activity, VU-29 inhibits SARS-CoV-2-induced cytotoxicity in Caco-2 cells by 4.01% at 10 µM concentration after 48 hours, as determined by high content imaging, and shows an inhibition rate of 0.65% in VERO-6 cells under similar conditions. The compound also inhibits the SARS-CoV-2 3CL-Pro protease by approximately 16.02% at 20 µM concentration, determined by the FRET response with a peptide substrate. Furthermore, in an enzymatic assay of human HDAC6, VU-29 demonstrates 23.02% inhibition with a commercial peptide substrate and 0.19% inhibition with a custom peptide substrate..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
VU-29 is a positive allosteric mGlu5 receptor modulator with an EC50 of 9 nM and a Ki of 244 nM for rmGluR5. It is selective for mGluR5 relative to other mGluR subtypes [EC50: rmGluR1/rmGluR2=557 nM/1.5 μM; hmGluR4=154 nM].
Targets&IC50
mGluR5 (rat):224 nM (Ki), mGluR5 (rat):9 nM (EC50), mGluR2 (rat):1.5 μM (EC50), mGluR4 (human):154 nM (EC50), mGluR1 (rat):557 nM (EC50)
SynonymsVU 29
Chemical Properties
Molecular Weight384.39
FormulaC22H16N4O3
Cas No.890764-36-0
SmilesN(C(=O)C1=CC=C(N(=O)=O)C=C1)C=2N(N=C(C2)C3=CC=CC=C3)C4=CC=CC=C4
Relative Density.1.30 g/cm3
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: 25 mg/mL (65.04 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6015 mL13.0076 mL26.0152 mL130.0762 mL
5 mM0.5203 mL2.6015 mL5.2030 mL26.0152 mL
10 mM0.2602 mL1.3008 mL2.6015 mL13.0076 mL
20 mM0.1301 mL0.6504 mL1.3008 mL6.5038 mL
50 mM0.0520 mL0.2602 mL0.5203 mL2.6015 mL

Calculator

  • Molarity Calculator
  • Dilution Calculator
  • Reconstitution Calculator
  • Molecular Weight 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:
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
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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

Keywords

Related Tags: buy VU-29 | purchase VU-29 | VU-29 cost | order VU-29 | VU-29 chemical structure | VU-29 formula | VU-29 molecular weight