Fig. 1 · Structure

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Fadolmidine hydrochloride

α2-AR Agonist

Fadolmidine hydrochloride is a selective agonist of the α2-adrenoceptor (α2-AR), exhibiting EC50 values of 0.4 nM, 4.9 nM, and 0.5 nM for the subtypes 2A, 2B, and 2C, respectively. This compound demonstrates significant analgesic properties across different pain modalities, including heat, mechanical, and visceral pain. Additionally, Fadolmidine hydrochloride effectively inhibits electrically induced contractions in the rat vas deferens, making it a valuable tool for studying pain mechanisms and potential therapies.

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Specifications

Manufacturer Adooq Bioscience
Actions Agonist
CAS Number 189353-32-0
Applications α2-AR Agonist
Formula C13H15ClN2O
Molecular Weight 250.72
SMILES
OC1=CC=C2C(C(CC2)CC3=CN=CN3)=C1.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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