Fig. 1 · Structure

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Conivaptan

Vasopressin V1A/V2 Receptor Antagonist

Conivaptan is a dual antagonist of the vasopressin V1A and V2 receptors. It has been shown to improve outcomes in congestive heart failure by ameliorating fluid retention and enhancing cardiac systolic function. This compound is valuable in research applications related to cardiovascular physiology and the modulation of water homeostasis.

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Specifications

Manufacturer Adooq Bioscience
Actions Antagonist
CAS Number 210101-16-9
Applications Vasopressin V1A/V2 Receptor Antagonist
Formula C32H26N4O2
Molecular Weight 498.57
Synonyms YM 087 free base
SMILES
O=C(C1=C(C2=CC=CC=C2)C=CC=C1)NC3=CC=C(C(N4C5=C(C6=C(CC4)N=C(C)N6)C=CC=C5)=O)C=C3

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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