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EntityQ419944· pop 18· linked from 614 articles

moxonidine

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Also known as Nucynt, BDF5896, Norcynt, BE5895, Cynt, (2R,4R)-1-[(2S)-5-[(aminoiminomethyl)amino]-1-oxo-2-[[(1,2,3,4-tetrahydro-3-methyl-8- quinolinyl)sulfonyl]amino]pentyl]-4-methyl-2-piperidinecarboxylic acid

Moxonidine (INN) is a new-generation alpha-2/imidazoline receptor agonist antihypertensive drug licensed for the treatment of mild to moderate essential hypertension. It may have a role when thiazides, beta-blockers, ACE inhibitors, and calcium channel blockers are not appropriate or have failed to control blood pressure. In addition, it demonstrates favourable effects on parameters of the insulin resistance syndrome, apparently independent of blood pressure reduction. It is also a growth hormone releaser. It is manufactured by Solvay Pharmaceuticals (acquired by Abbott in 2009) under the bran

Research

676 papers

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Wikidata facts

Mass
241.073038
Show 4 more facts
chemical formula
C₉H₁₂ClN₅O
canonical SMILES
CC1=NC(=C(C(=N1)Cl)NC2=NCCN2)OC
defined daily dose
0.3
Commons category
Moxonidine
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~4 min read

Article

10 sections
Contents
  • Mechanism of action
  • Pharmacodynamic properties
  • Effects on insulin resistance
  • Contraindications
  • Adverse effects
  • Safety
  • Drug interactions
  • See also
  • References
  • External links

Moxonidine (INN) is a new-generation alpha-2/imidazoline receptor agonist antihypertensive drug licensed for the treatment of mild to moderate essential hypertension. It may have a role when thiazides, beta-blockers, ACE inhibitors, and calcium channel blockers are not appropriate or have failed to control blood pressure. In addition, it demonstrates favourable effects on parameters of the insulin resistance syndrome, apparently independent of blood pressure reduction. It is also a growth hormone releaser. It is manufactured by Solvay Pharmaceuticals (acquired by Abbott in 2009) under the brand name Physiotens and Moxon.

==Mechanism of action== Moxonidine is a selective agonist at the imidazoline receptor subtype 1 (I1). This receptor subtype is found in both the rostral ventro-lateral pressor and ventromedial depressor areas of the medulla oblongata. Moxonidine therefore causes a decrease in sympathetic nervous system activity and, therefore, a decrease in blood pressure.

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