Moxonidine hydrochloride

Moxonidine hydrochloride Basic information
Product Name:Moxonidine hydrochloride
Synonyms:MOXONIDINE HYDROCHLORIDE;MOXONIDINE HCL;BDF-5895 HCL;4-CHLORO-6-METHOXY-2-METHYL-5-(2-IMIDAZOLIN-2-YL)AMINOPYRIMIDINE HCL;4-CHLORO-N-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)-6-METHOXY-2-METHYL-5-PYRIMIDINAMINE HYDROCHLORIDE;MoxonidineHclC9H12C1N50.HC1;4-Chloro-N-(4,5-dihydro-1H-imidazol-2-yl)-6-methoxy-2-methyl-3H-pyrimidin-2-amine hydrochloride;BDF-5895, 4-Chloro-6-methoxy-2-methyl-5-(2-imidazolin-2-yl)aminopyrimidine hydrochloride
CAS:75438-58-3
MF:C9H13Cl2N5O
MW:278.14
EINECS:
Product Categories:Imidazoline binding site;Antihypertensive
Mol File:75438-58-3.mol
Moxonidine hydrochloride Structure
Moxonidine hydrochloride Chemical Properties
Melting point 189°
CAS DataBase Reference75438-58-3(CAS DataBase Reference)
Safety Information
WGK Germany 3
RTECS UV6260290
MSDS Information
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SigmaAldrich English
Moxonidine hydrochloride Usage And Synthesis
DescriptionMoxonidine hydrochloride is a centrally acting antihypertensive agent. Mixed I1 imidazoline receptor and α2-adrenergic agonist; displays 40-fold higher affinity for I1 receptors versus α2-adrenoceptors.
Moxonidine is a selective high-affinity imidazoline I1-receptor agonist and a selectively low-affinity α2-adrenoceptor agonist. It exhibits anti-hypertensive properties by reducing blood pressure efficiently. Moxonidine also exhibits spinal analgesic activity through the α2C-adrenoceptor component.
UsesMoxonidine is a new-generation centrally acting antihypertensive drug approved for the treatment of mild to moderate essential hypertension. It is suggested to be effective in cases where other agents such as thiazides, beta-blockers, ACE inhibitors, and calcium channel blockers are not appropriate or irresponsive. As well, moxonidine has been shown to present blood pressure-independent beneficial effects on insulin resistance syndrome.
Moxonidine hydrochloride is used as antihypertensive agent. It has been reported to produce dose-dependent analgesia in multiple acute pain assays and has been reported to potently inhibit the binding of [3H]-clonidine to VLM (ventrolateral medulla) membranes in a dose-dependent manner with the IC50 value of 53 ± 10nM.
ApplicationMoxonidine hydrochloride has been used:
as a standard to study its blood-brain barrier (BBB) permeability in porcine brain lipid extract by parallel artificial membrane permeability assay (PAMPA) method.
as a standard to study the chromatographic behavior and lipophilicity by reversed-phase thin-layer chromatography (RP-TLC).
as an imidazoline I1 receptor agonist to study its effects on excitatory inputs in airway vagal preganglionic neuron (AVPN).
Biological ActivityMoxonidine is a selective high-affinity imidazoline I1-receptor agonist and a selectively low-affinity α2-adrenoceptor agonist. It exhibits anti-hypertensive properties by reducing blood pressure efficiently. Moxonidine also exhibits spinal analgesic activity through the α2C-adrenoceptor component.
Moxonidine hydrochloride Preparation Products And Raw materials
Fexofenadine hydrochloride Methyl Ramosetron hydrochloride Propacetamol Imidazoline inhibitor Topotecan hydrochloride Clonidine hydrochloride Methoxy 2-Methoxyethanol Anisole (Trifluoromethoxy)benzene Cinchonidine Difluorochloromethane Imidazolidine Moxonidine Moxonidine hydrochloride Dihydromyrcenol Tizanidine

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