Fig. 1 · Structure
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Satavaptan
Vasopressin Receptor Antagonist
Satavaptan is a selective antagonist of the vasopressin V2 receptor. By inhibiting this receptor, Satavaptan modulates vasopressin-regulated phosphopeptides and disrupts vasopressin-mediated signaling pathways. This compound shows promise in the treatment of hyponatremia, making it a valuable tool for research in fluid balance and electrolyte homeostasis.
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Specifications
| Manufacturer | Adooq Bioscience |
|---|---|
| Actions | Antagonist |
| CAS Number | 185913-78-4 |
| Applications | Vasopressin Receptor Antagonist |
| Formula | C33H45N3O8S |
| Molecular Weight | 643.79 |
| Synonyms | SR 121463 |
| SMILES | O=C(NC(C)(C)C)C1=CC=C(S(=O)(N2C([C@@]3(C4=C2C=CC(OCC)=C4)CC[C@H](OCCN5CCOCC5)CC3)=O)=O)C(OC)=C1 |
Storage & Solubility
In Vitro Solubility
Reported Solubility
No reported solubility data are available for this product.
Preparing Stock Solutions
| Concentration | |
|---|---|
Values use four significant digits. Prepare to the final solution volume; this is not the volume of solvent to add.
Stock preparation is unavailable for this product molecular weight.
Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.
Storage
Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.