Fig. 1 · Structure

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Imidafenacin hydrochloride

M1/M3 Receptor Inhibitor

Imidafenacin hydrochloride is an orally active inhibitor of muscarinic M1 and M3 receptors. It effectively inhibits bladder contraction in vivo, demonstrating significant antidiuretic effects through the enhancement of vasopressin signaling. This compound is particularly relevant for research focused on overactive bladder and related conditions, making it a valuable tool in the study of urinary disorders.

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Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 893421-54-0
Applications M1/M3 Receptor Inhibitor
Formula C20H22ClN3O
Molecular Weight 355.86
Synonyms KRP-197 (hydrochloride); ONO-8025 (hydrochloride)
SMILES
O=C(N)C(C1=CC=CC=C1)(C2=CC=CC=C2)CCN3C=CN=C3C.[H]Cl

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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