Details
Stereochemistry | ACHIRAL |
Molecular Formula | C9H12ClN5O |
Molecular Weight | 241.677 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(NC2=NCCN2)C(Cl)=NC(C)=N1
InChI
InChIKey=WPNJAUFVNXKLIM-UHFFFAOYSA-N
InChI=1S/C9H12ClN5O/c1-5-13-7(10)6(8(14-5)16-2)15-9-11-3-4-12-9/h3-4H2,1-2H3,(H2,11,12,15)
Moxonidine is a second-generation, centrally acting antihypertensive drug with a distinctive mode of action. Moxonidine activates I1-imidazoline receptors (I1-receptors). Imidazoline I1-receptor agonism represents a new mode of antihypertensive action to inhibit peripheral alpha-adrenergic tone by a central mechanism. Adrenaline, noradrenaline and renin levels are reduced, a finding consistent with central inhibition of sympathetic tone. Moxonidine acts centrally to reduce peripheral sympathetic activity, thus decreasing peripheral vascular resistance. In patients with mild to moderate hypertension, moxonidine reduces blood pressure (BP) as effectively as most first-line antihypertensives when used as monotherapy and is also an effective adjunctive therapy in combination with other antihypertensive agents. It improves the metabolic profile in patients with hypertension and diabetes mellitus or impaired glucose tolerance, is well tolerated, has a low potential for drug interactions and may be administered once daily in most patients. Moxonidine is a good option in the treatment of patients with mild to moderate hypertension, particularly as adjunctive therapy in patients with the metabolic syndrome.
CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: Q9Y2I1|||Q9UFW3 Gene ID: 11188.0 Gene Symbol: NISCH Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/8380858 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | PHYSIOTENS Approved UsePhysiotens is indicated for the treatment of hypertension. |
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Palliative | Unknown Approved UseUnknown |
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Palliative | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
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Cardiovascular effects of rilmenidine, moxonidine and clonidine in conscious wild-type and D79N alpha2A-adrenoceptor transgenic mice. | 1999 Mar |
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[Use of phisiotens for the treatment of arterial hypertension in elderly patients]. | 2001 |
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Safety and efficacy of moxonidine in mild to moderate hypertension. | 2001 Aug |
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The underreporting of results and possible mechanisms of 'negative' drug trials in patients with chronic heart failure. | 2001 Aug |
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Interactions of ligands at angiotensin II-receptors and imidazoline receptors. | 2001 Feb |
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Pharmacodynamic models for the cardiovascular effects of moxonidine in patients with congestive heart failure. | 2001 Jan |
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[Effect of moxonidine on the cardiac chronotropic regulation in hypertensive rats SHR-SP]. | 2001 Jan-Feb |
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[Imidazoline receptors-normal and pathological factors]. | 2001 Jul-Sep |
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Lowering of microalbuminuria in diabetic patients by a sympathicoplegic agent: novel approach to prevent progression of diabetic nephropathy? | 2001 Mar |
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[Clinical assessment of prolonged therapy of patients with hypertension and diabetes with imidazoline receptor agonist moxonidine]. | 2002 |
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[Moxomidine effectiveness in women with arterial hypertension associated with metabolic syndrome in initially high heart rate]. | 2002 |
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Placebo-controlled comparison of the efficacy and tolerability of once-daily moxonidine and enalapril in mild to moderate essential hypertension. | 2002 |
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Effects of central sympathetic inhibition on heart rate variability during steady-state exercise in healthy humans. | 2002 Jan |
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alpha(2C)-Adrenergic receptors mediate spinal analgesia and adrenergic-opioid synergy. | 2002 Jan |
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[Conformational study of drugs which affect I1-imidazoline receptors]. | 2002 Jul |
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[125I]2-(2-chloro-4-iodo-phenylamino)-5-methyl-pyrroline (LNP 911), a high-affinity radioligand selective for I1 imidazoline receptors. | 2002 Jul |
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Naphazoline-induced neuroendocrine changes: increases in ANP and cGMP levels, but suppression of NE, 3H-NE, and cAMP levels in rabbit eyes. | 2002 Jul |
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Imidazoline receptors in the heart: characterization, distribution, and regulation. | 2002 Jun |
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Down-regulation of platelet imidazoline-1-binding sites after bupropion treatment. | 2002 Mar |
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Contractile responses of the rat vas deferens after epithelium removal. | 2002 May 3 |
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Characterization of sucrose-induced changes in cardiac phenotype. | 2002 Oct |
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Restored capillary density in spared myocardium of infarcted rats improves ischemic tolerance. | 2002 Sep |
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Pertussis toxin converts hyperpolarizations caused by alpha(2)-adrenoceptor agonists containing an imidazoline moiety into depolarizations in MIN 6 cells. | 2002 Sep |
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[Current views on migraine and anti-migraine preparations]. | 2003 |
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Effects of moxonidine and metoprolol in penile circulation in hypertensive men with erectile dysfunction: results of a pilot study. | 2003 Aug |
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The role of I(1)-imidazoline and alpha(2)-adrenergic receptors in the modulation of glucose metabolism in the spontaneously hypertensive obese rat model of metabolic syndrome X. | 2003 Aug |
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Apparent absence of direct renal effect of imidazoline receptor agonists. | 2003 Dec |
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Moxonidine and central alpha2 adrenergic receptors in sodium intake. | 2003 Dec 12 |
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Importance of imidazoline-preferring receptors in the cardiovascular actions of chronically administered moxonidine, rilmenidine and clonidine in conscious rabbits. | 2003 Jan |
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Antihypertensive efficacy of moxonidine in primary care: a 'real-life' study. | 2003 Jul-Aug |
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Experimental approach to differentiation of the effects mediated by imidazole receptors and alpha2-adrenoceptors on platelets. | 2003 Jun |
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Adverse mortality effect of central sympathetic inhibition with sustained-release moxonidine in patients with heart failure (MOXCON). | 2003 Oct |
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Central moxonidine on salivary gland blood flow and cardiovascular responses to pilocarpine. | 2003 Oct 17 |
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The effects of imidazoline agents on the aggregation of human platelets. | 2004 Feb |
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The I1-imidazoline agonist moxonidine decreases sympathetic tone under physical and mental stress. | 2004 May |
Sample Use Guides
In Vivo Use Guide
Sources: https://gp2u.com.au/static/pdf/P/PHYSIOTENS-PI.pdf
Treatment should be started with 0.2 mg Physiotens in the morning. The dose may be titrated after two weeks to 0.4 mg given as one dose or as divided doses (morning and evening) until a satisfactory response is achieved. If the response is still unsatisfactory after a further 2 weeks treatment, the dosage can be increased up to a maximum of 0.6 mg in divided doses (morning and evening). A single daily dose of 0.4 mg and a divided daily dose of 0.6 mg of Physiotens should not be exceeded. Physiotens may be taken with or without food.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15305091
It was investigate the effects of moxonidine on neurons in the rostral ventrolateral medulla (RVLM) with electrophysiological properties similar to premotor sympathetic neurons in vivo. Moxonidine (2-10 microM) was applied to the perfusate on 4 irregularly firing neurons, and 2 regularly firing neurons. Moxonidine (2 microM) produced only minor depolarization in 2 of these neurons. However, on 4 tested neurons, moxonidine (10 microM) elicited a profound inhibitory effect with hyperpolarization (near -20 mV); these neurons practically ceased firing. These changes were partially reversible. The results would indicate that neurons in the RVLM, recorded in vitro and with similar electrophysiological characteristics to a group of neurons previously identified in vivo in the same bulbar region as barosensitive premotor sympathetic neurons, can be modulated by imidazoline-derivative adrenergic agonists. These results could help to understand the hypotensive effects of moxonidine.
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ACTIVE MOIETY
METABOLITE (PARENT)