Fig. 1 · Structure
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Invopressin
V1A Receptor Agonist
Invopressin is a partial agonist of the V1A vasopressin receptor, exhibiting an EC50 of 1.0 nM. It is primarily utilized in research focused on cirrhosis-related conditions, including bacterial peritonitis, hepatorenal syndrome type 2 (HRS2), and refractory ascites. This compound enables the investigation of therapeutic strategies targeting vasopressin-mediated pathways in these clinical scenarios.
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Specifications
| Manufacturer | Adooq Bioscience |
|---|---|
| Actions | Partial Agonist |
| CAS Number | 1488411-60-4 |
| Applications | V1A Receptor Agonist |
| Formula | C110H161N31O27S2 |
| Molecular Weight | 2413.78 |
| Synonyms | OCE-205 |
| SMILES | C(=O)(N1[C@H](C(N[C@@H](CCNC([C@H](CCCCNC([C@@H](NC(CC[C@H](NC([C@@H](NC(=O)[C@H]2N(C([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CC3=CC=CC=C3)NC([C@@H](CC4=CC=C(OC)C=C4)NC(CC5=CC=CC=C5)=O)=O)=O)CCC(N)=O)=O)CC(N)=O)=O)C)=O)CCC2)CCCNC(=N)N)=O)C(N)=O)=O)CCCCNC(C)=O)=O)N)=O)C(NCC(N)=O)=O)=O)CCC1)[C@H]6NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@]([C@H](CC)C)(NC(=O)[C@H](CC7=CC=CC=C7)NC(=O)[C@@H](N)CSSC6)[H] |
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.