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OBA-09 (2-oxopropanoyloxy benzoic acid) is a novel multimodal neuroprotectant synthesized as a hybrid of salicylic acid and pyruvate. Designed to synergize the anti-inflammatory properties of salicylic acid with the metabolic support and antioxidant capacity of pyruvate, OBA-09 combats ischemic brain injury effectively. It exhibits potent radical scavenging activity against superoxide, hydroxyl radicals, and hydrogen peroxide. Furthermore, it attenuates post-ischemic inflammation by inhibiting the NF-kB signaling pathway and the release of HMGB1. In stroke models, OBA-09 significantly reduces infarct volume and improves neurological scores.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $30 | - | In Stock | |
| 5 mg | $55 | - | In Stock | |
| 10 mg | $89 | - | In Stock | |
| 25 mg | $148 | - | In Stock | |
| 50 mg | $219 | - | In Stock | |
| 100 mg | $326 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $61 | - | In Stock |
| Description | OBA-09 (2-oxopropanoyloxy benzoic acid) is a novel multimodal neuroprotectant synthesized as a hybrid of salicylic acid and pyruvate. Designed to synergize the anti-inflammatory properties of salicylic acid with the metabolic support and antioxidant capacity of pyruvate, OBA-09 combats ischemic brain injury effectively. It exhibits potent radical scavenging activity against superoxide, hydroxyl radicals, and hydrogen peroxide. Furthermore, it attenuates post-ischemic inflammation by inhibiting the NF-kB signaling pathway and the release of HMGB1. In stroke models, OBA-09 significantly reduces infarct volume and improves neurological scores. |
| In vitro | In cell-free assays, OBA-09 acted as a robust ROS scavenger, effectively neutralizing hydroxyl radicals (OH), superoxide anions (O2.-), and hydrogen peroxide (H2O2). In neuronal cultures, it inhibited the DNA binding activity of NF-kB and suppressed the degradation of IkB-alpha, leading to decreased expression of proinflammatory enzymes like iNOS and COX-2 [1][2]. |
| In vivo | In a rat model of middle cerebral artery occlusion (MCAO), systemic administration of OBA-09 (50-100 mg/kg, intraperitoneal) significantly reduced brain infarct volume and improved neurological deficits. It effectively lowered the levels of proinflammatory cytokines (IL-1beta, TNF-alpha) and prevented the nucleocytoplasmic translocation and subsequent release of HMGB1 in the ischemic brain [1][2]. |
| Molecular Weight | 208.17 |
| Formula | C10H8O5 |
| Cas No. | 856095-68-6 |
| Smiles | O=C(O)C=1C=CC=CC1OC(=O)C(=O)C |
| Relative Density. | no data available |
| 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: 80 mg/mL (384.3 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween-80+45% Saline: 2.4 mg/mL (11.53 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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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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