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

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $38 | - | In Stock | |
| 50 mg | $58 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $29 | - | In Stock |
| 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]. |
| Molecular Weight | 314.32 |
| Formula | C15H10N2O4S |
| Cas No. | 439946-22-2 |
| Smiles | Nc1c(sc2[nH]c(=O)c(cc12)C(O)=O)C(=O)c1ccccc1 |
| Relative Density. | 1.554 g/cm3 (Predicted) |
| 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: 83 mg/mL (264.06 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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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.
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.
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