U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of MOXONIDINE

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)

HIDE SMILES / InChI
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.

Originator

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q9Y2I1|||Q9UFW3
Gene ID: 11188.0
Gene Symbol: NISCH
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
PHYSIOTENS

Approved Use

Physiotens is indicated for the treatment of hypertension.
Palliative
Unknown

Approved Use

Unknown
Palliative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Cardiovascular effects of rilmenidine, moxonidine and clonidine in conscious wild-type and D79N alpha2A-adrenoceptor transgenic mice.
1999 Mar
[Use of phisiotens for the treatment of arterial hypertension in elderly patients].
2001
Safety and efficacy of moxonidine in mild to moderate hypertension.
2001 Aug
The underreporting of results and possible mechanisms of 'negative' drug trials in patients with chronic heart failure.
2001 Aug
Interactions of ligands at angiotensin II-receptors and imidazoline receptors.
2001 Feb
Pharmacodynamic models for the cardiovascular effects of moxonidine in patients with congestive heart failure.
2001 Jan
[Effect of moxonidine on the cardiac chronotropic regulation in hypertensive rats SHR-SP].
2001 Jan-Feb
[Imidazoline receptors-normal and pathological factors].
2001 Jul-Sep
Lowering of microalbuminuria in diabetic patients by a sympathicoplegic agent: novel approach to prevent progression of diabetic nephropathy?
2001 Mar
[Clinical assessment of prolonged therapy of patients with hypertension and diabetes with imidazoline receptor agonist moxonidine].
2002
[Moxomidine effectiveness in women with arterial hypertension associated with metabolic syndrome in initially high heart rate].
2002
Placebo-controlled comparison of the efficacy and tolerability of once-daily moxonidine and enalapril in mild to moderate essential hypertension.
2002
Effects of central sympathetic inhibition on heart rate variability during steady-state exercise in healthy humans.
2002 Jan
alpha(2C)-Adrenergic receptors mediate spinal analgesia and adrenergic-opioid synergy.
2002 Jan
[Conformational study of drugs which affect I1-imidazoline receptors].
2002 Jul
[125I]2-(2-chloro-4-iodo-phenylamino)-5-methyl-pyrroline (LNP 911), a high-affinity radioligand selective for I1 imidazoline receptors.
2002 Jul
Naphazoline-induced neuroendocrine changes: increases in ANP and cGMP levels, but suppression of NE, 3H-NE, and cAMP levels in rabbit eyes.
2002 Jul
Imidazoline receptors in the heart: characterization, distribution, and regulation.
2002 Jun
Down-regulation of platelet imidazoline-1-binding sites after bupropion treatment.
2002 Mar
Contractile responses of the rat vas deferens after epithelium removal.
2002 May 3
Characterization of sucrose-induced changes in cardiac phenotype.
2002 Oct
Restored capillary density in spared myocardium of infarcted rats improves ischemic tolerance.
2002 Sep
Pertussis toxin converts hyperpolarizations caused by alpha(2)-adrenoceptor agonists containing an imidazoline moiety into depolarizations in MIN 6 cells.
2002 Sep
[Current views on migraine and anti-migraine preparations].
2003
Effects of moxonidine and metoprolol in penile circulation in hypertensive men with erectile dysfunction: results of a pilot study.
2003 Aug
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
Apparent absence of direct renal effect of imidazoline receptor agonists.
2003 Dec
Moxonidine and central alpha2 adrenergic receptors in sodium intake.
2003 Dec 12
Importance of imidazoline-preferring receptors in the cardiovascular actions of chronically administered moxonidine, rilmenidine and clonidine in conscious rabbits.
2003 Jan
Antihypertensive efficacy of moxonidine in primary care: a 'real-life' study.
2003 Jul-Aug
Experimental approach to differentiation of the effects mediated by imidazole receptors and alpha2-adrenoceptors on platelets.
2003 Jun
Adverse mortality effect of central sympathetic inhibition with sustained-release moxonidine in patients with heart failure (MOXCON).
2003 Oct
Central moxonidine on salivary gland blood flow and cardiovascular responses to pilocarpine.
2003 Oct 17
The effects of imidazoline agents on the aggregation of human platelets.
2004 Feb
The I1-imidazoline agonist moxonidine decreases sympathetic tone under physical and mental stress.
2004 May
Patents

Sample Use Guides

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
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.
Name Type Language
MOXONIDINE
EP   INN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
MOXONIDINE [MART.]
Common Name English
BE5895
Code English
BE-5895
Code English
LY326869
Code English
5-PYRIMIDINAMINE, 4-CHLORO-N-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)-6-METHOXY-2-METHYL-
Systematic Name English
LY-326869
Code English
Moxonidine [WHO-DD]
Common Name English
CYNT
Brand Name English
BDF-5896
Code English
4-Chloro-5-(2-imidazolidinyldeneamino)-6-methoxy-2-methylpyrimidine
Common Name English
moxonidine [INN]
Common Name English
MOXONIDINE [USAN]
Common Name English
MOXONIDINE [MI]
Common Name English
MOXONIDINE [EP MONOGRAPH]
Common Name English
BDF5896
Code English
Classification Tree Code System Code
WHO-ATC C02LC05
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
WHO-VATC QC02LC05
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
WHO-ATC C02AC05
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
NCI_THESAURUS C270
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
WHO-VATC QC02AC05
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
Code System Code Type Description
INN
5207
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
FDA UNII
CC6X0L40GW
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
NCI_THESAURUS
C87629
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
SMS_ID
100000088399
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
MESH
C043482
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
CAS
75438-57-2
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
USAN
KK-103
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
PUBCHEM
4810
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
ChEMBL
CHEMBL19236
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
MERCK INDEX
m7649
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY Merck Index
RXCUI
30257
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PRIMARY RxNorm
EVMPD
SUB09092MIG
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
DRUG BANK
DB09242
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
EPA CompTox
DTXSID5045170
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
WIKIPEDIA
MOXONIDINE
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY
DRUG CENTRAL
1856
Created by admin on Fri Dec 15 15:46:52 GMT 2023 , Edited by admin on Fri Dec 15 15:46:52 GMT 2023
PRIMARY