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α2A-AR agonist 1

α2A-AR agonist 1 (Compound B9) is a selective agonist for α2-adrenergic receptor (α2A-AR) with EC50 of 0.23 nM. α2A-AR agonist 1 exhibits a hypnotic effect, with ED50 of 0.138 mg/kg in the loss of righting reflex (LORR) experiment. α2A-AR agonist 1 exhibits metabolic stability in mouse liver microsomes[1].

Product Specifications

CAS Number

2971825-58-6

UNSPSC

12352005

Target

Adrenergic Receptor

Type

Reference compound

Related Pathways

GPCR/G Protein; Neuronal Signaling

Field of Research

Cancer

Assay Protocol

https://www.medchemexpress.com/α2a-ar-agonist-1.html

Purity

99.92

Solubility

DMSO : 87.5 mg/mL (ultrasonic)

Smiles

BrC1=C(C2=CC=C1)OCCC2C3=CNC=N3

Molecular Formula

C12H11BrN2O

Molecular Weight

279.13

References & Citations

[1]Lv X, et al., Designing Chromane Derivatives as α2A-Adrenoceptor Selective Agonists via Conformation Constraint. J Med Chem. 2024 Jun 18.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

α adrenergic receptor

Available Sizes

Frequently Asked Questions

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