Fig. 1 · Structure

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Velmupressin acetate

V2R Agonist

Velmupressin acetate is a selective and potent agonist of the V2 receptor (V2R), exhibiting EC50 values of 0.07 nM and 0.02 nM for human and rat V2R, respectively. This peptidic compound is characterized by its short-acting nature, making it suitable for studies involving renal physiology and water homeostasis. Velmupressin acetate can be used in research applications focused on the modulation of water reabsorption and the investigation of vasopressin-related signaling pathways.

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Specifications

Manufacturer Adooq Bioscience
Actions Agonist
CAS Number 1647120-04-4
Applications V2R Agonist
Formula C44H64ClN11O10S2
Molecular Weight 1006.63
Synonyms c(Bua-Cpa-Thi-Val-Asn-Cys)-Pro-d-Arg-NEt2 acetate
SMILES
C(C)(O)=O.C(=O)(N1[C@H](C(NCCCCNC(=N)N)=O)CCC1)[C@H]2NC(=O)[C@H](CC(N)=O)NC(=O)[C@H]([C@@H](C)C)NC(=O)[C@H](CC3=CC=CS3)NC(=O)[C@H](CC4=CC=C(Cl)C=C4)NC(=O)CCCSC2

Storage & Solubility

In Vitro Solubility

Reported Solubility

No reported solubility data are available for this product.

Preparing Stock Solutions

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.

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