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ONO 1301 is a prostaglandin I2 mimetic compound with inhibitory activity against thromboxane A2 synthase, and it suppresses pancreatic fibrosis in the DBTC-induced chronic pancreatitis model by inhibiting monocyte activity through both direct effects of ONO 1301 and induction of hepatocyte growth factor. ONO 1301 also promoting HGF synthesis and elevating intracellular cyclic AMP levels via IP-receptor signaling, highlighting its therapeutic relevance in fibrotic disease and inflammation research.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $68 | 6-8 weeks | 6-8 weeks | |
| 5 mg | $163 | 6-8 weeks | 6-8 weeks | |
| 10 mg | $289 | 6-8 weeks | 6-8 weeks | |
| 25 mg | $595 | 6-8 weeks | 6-8 weeks | |
| 50 mg | $987 | 6-8 weeks | 6-8 weeks | |
| 100 mg | $1,730 | 6-8 weeks | 6-8 weeks | |
| 1 mL x 10 mM (in DMSO) | $179 | 6-8 weeks | 6-8 weeks |
| Description | ONO 1301 is a prostaglandin I2 mimetic compound with inhibitory activity against thromboxane A2 synthase, and it suppresses pancreatic fibrosis in the DBTC-induced chronic pancreatitis model by inhibiting monocyte activity through both direct effects of ONO 1301 and induction of hepatocyte growth factor. ONO 1301 also promoting HGF synthesis and elevating intracellular cyclic AMP levels via IP-receptor signaling, highlighting its therapeutic relevance in fibrotic disease and inflammation research. |
| Targets&IC50 | Collagen-induced platelet aggregation:460 nM |
| In vitro | In platelet function assays, ONO 1301 inhibited collagen-induced platelet aggregation in a concentration-dependent manner with an IC50 of 460 nM. Additionally, in primary osteoblasts and ST2 stromal cells, treatment with the compound (0-1000 nM) significantly increased alkaline phosphatase (ALP) activity, serving as a marker for osteoblast differentiation [1]. |
| Synonyms | ONO-AP 500-02, ONO-1301, ONO1301 |
| Molecular Weight | 428.48 |
| Formula | C26H24N2O4 |
| Cas No. | 176391-41-6 |
| Smiles | C(CO/N=C(\C1=CC=CC=C1)/C=2C=CC=NC2)C=3C=4C(=C(OCC(O)=O)C=CC4)CCC3 |
| Relative Density. | 1.21 g/cm3 (Predicted) |
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 40 mg/mL (93.35 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
DMSO
| |||||||||||||||||||||||||||||||
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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