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ZB-R-55 is an orally available and highly potent bimodal RIPK1 inhibitor with excellent kinase selectivity in lps-induced sepsis models for the study of SIRS and sepsis.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $333 | - | In Stock | |
| 5 mg | $987 | - | In Stock | |
| 10 mg | $1,360 | - | In Stock | |
| 25 mg | $1,980 | - | In Stock |
| Description | ZB-R-55 is an orally available and highly potent bimodal RIPK1 inhibitor with excellent kinase selectivity in lps-induced sepsis models for the study of SIRS and sepsis. |
| In vitro | ZB-R-55 exhibits 10 times greater inhibitory activity against RIPK1 compared to GSK2982772, demonstrating exceptional kinase selectivity.[1] |
| In vivo | In an LPS/TNF-α-induced sepsis mouse model, oral administration of ZB-R-55 (10 mg/kg) significantly alleviated hypothermia, reduced cytokine storm, and improved survival rate. [2] |
| Synonyms | ZBR-55, ZB-R55 |
| Molecular Weight | 441.48 |
| Formula | C25H23N5O3 |
| Cas No. | 2416593-55-8 |
| Smiles | CN1C=2C(OC[C@H](NC(=O)C=3NC(CC4=CC=CC=C4)=NN3)C1=O)=CC=C(C#CC5CC5)C2 |
| Color | White |
| Appearance | Solid |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (181.21 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 3.3 mg/mL (7.47 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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