Moxonidine
Moxonidine (BDF5895) is an orally active imidazoline type 1 receptor (I1-R) agonist. Moxonidine activates imidazoline I1 receptors and α2 adrenoceptors, affecting oxidized low-density lipoprotein uptake. Moxonidine reduces atherosclerotic lesions and lowers blood pressure. Moxonidine can be used in the study of hypertension, heart failure, and atherosclerosis[1][2][3][4][5][6][7].
Product Specifications
CAS Number
[75438-57-2]
Product Name Alternative
BDF5895
UNSPSC
12352005
Hazard Statement
H301, H411
Target
Adrenergic Receptor; Imidazoline Receptor; LDLR
Type
Reference compound
Related Pathways
GPCR/G Protein; Metabolic Enzyme/Protease; Neuronal Signaling
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease; Cardiovascular Disease
Assay Protocol
https://www.medchemexpress.com/moxonidine.html
Concentration
10mM
Purity
99.72
Solubility
DMSO : 20 mg/mL (ultrasonic)
Smiles
CC1=NC(OC)=C(NC2=NCCN2)C(Cl)=N1
Molecular Formula
C9H12ClN5O
Molecular Weight
241.68
Precautions
H301, H411
References & Citations
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
Launched
Available Sizes
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