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UCPH-101 is an inhibitor of excitatory amino acid transporter subtype 1 (EAAT1) with an IC50 of 0.66 μM.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $45 | In Stock | In Stock | |
| 2 mg | $73 | In Stock | In Stock | |
| 5 mg | $139 | In Stock | In Stock | |
| 10 mg | $226 | In Stock | In Stock | |
| 25 mg | $455 | In Stock | In Stock | |
| 50 mg | $728 | In Stock | In Stock | |
| 100 mg | $1,060 | In Stock | In Stock | |
| 200 mg | $1,430 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $153 | In Stock | In Stock |
| Description | UCPH-101 is an inhibitor of excitatory amino acid transporter subtype 1 (EAAT1) with an IC50 of 0.66 μM. |
| Targets&IC50 | EAAT1:0.66 μM. |
| In vitro | Preincubation with 100 μM UCPH-101 results in a notable reduction in the expression levels of HA-EAAT1 and HA-GLAST. Additionally, UCPH-101 and UCPH-102 exhibit concentration-dependent inhibition of EAAT1 anion currents, with dissociation constant (KD) values of 0.34±0.03 μM (Hill=1.3±0.13, n≥9) for UCPH-101 and 0.17±0.02 μM (Hill=0.97±0.11, n≥7) for UCPH-102. |
| Synonyms | UCPH 101 |
| Molecular Weight | 422.48 |
| Formula | C27H22N2O3 |
| Cas No. | 1118460-77-7 |
| Smiles | COc1ccc(cc1)C1C(C#N)=C(N)OC2=C1C(=O)CC(C2)c1cccc2ccccc12 |
| Relative Density. | 1.32 g/cm3 (Predicted) |
| Color | White |
| Appearance | Solid |
| 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: 18.85 mg/mL (44.62 mM), Sonication is recommended. | |||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (4.73 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | |||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||
DMSO
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