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A-317491 sodium salt hydrate是一种非核苷酸的P2X3和P2X2/3受体拮抗剂，可抑制受体介导的钙通量。
| In vitro | DMSO | 90 mg/mL (159.13 mM) | |
| Water | Insoluble | ||
| Ethanol | 90 mg/mL (159.13 mM) | ||
|
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
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| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.1 mM | 17.68 mL | 88.41 mL | 176.81 mL |
| 0.5 mM | 3.54 mL | 17.68 mL | 35.36 mL |
| 1 mM | 1.77 mL | 8.84 mL | 17.68 mL |
| 5 mM | 0.35 mL | 1.77 mL | 3.54 mL |
*The above data is based on the productmolecular weight 565.57. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
| 目录号 | A12412 |
|---|---|
| 作用机制 | Antagonist (拮抗剂) |
| M. Wt | 565.57 |
| Formula | C33H27N1O8 |
| Purity | >99% |
| Storage | Store lyophilized at -20ºC, keep desiccated. |
| CAS No. | 475205-49-3 |
| Synonyms | A317491 |
| SMILES | C1C[C@@H](C2=CC=CC=C2C1)N(CC3=CC(=CC=C3)OC4=CC=CC=C4)C(=O)C5=CC(=C(C=C5C(=O)O)C(=O)O)C(=O)O |
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