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LDN-91946

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Catalog No. T15729Cas No. 439946-22-2

LDN-91946 is an effective and selective inhibitor of ubiquitin C-terminal hydrolase-L1 (UCH-L1) (Ki = 2.8 μM).

LDN-91946

LDN-91946

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Purity: 97.12%
Catalog No. T15729Cas No. 439946-22-2
LDN-91946 is an effective and selective inhibitor of ubiquitin C-terminal hydrolase-L1 (UCH-L1) (Ki = 2.8 μM).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$38-In Stock
50 mg$58-In Stock
1 mL x 10 mM (in DMSO)$29-In Stock
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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.
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Purity:97.12%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
LDN-91946 is an effective and selective inhibitor of ubiquitin C-terminal hydrolase-L1 (UCH-L1) (Ki = 2.8 μM).
Targets&IC50
UCHL1: 2.8 μM(ki)
In vitro
LDN-91946 demonstrates no inhibitory activity against TGase 2, Papain, and Caspase-3 at concentrations of 40 μM, and remains inactive against UCH-L3 at 20 μM. Furthermore, it exhibits no cytotoxic effects on serum-starved Neuro 2A (N2A) cells even at concentrations up to 0.1 mM[1].
Chemical Properties
Molecular Weight314.32
FormulaC15H10N2O4S
Cas No.439946-22-2
SmilesNc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1ccccc1
Relative Density.1.554 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: 83 mg/mL (264.06 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1815 mL15.9074 mL31.8147 mL159.0736 mL
5 mM0.6363 mL3.1815 mL6.3629 mL31.8147 mL
10 mM0.3181 mL1.5907 mL3.1815 mL15.9074 mL
20 mM0.1591 mL0.7954 mL1.5907 mL7.9537 mL
50 mM0.0636 mL0.3181 mL0.6363 mL3.1815 mL
100 mM0.0318 mL0.1591 mL0.3181 mL1.5907 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:
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
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Dose Conversion

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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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