Chemistry:Emoxypine
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| Trade names | Mexidol |
| Other names | Emoxipine, Emoxypin, Epigid, 6-Methyl-2-ethyl-3-hydroxypyridine |
| Routes of administration | Oral & IV |
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| Elimination half-life | 2-2.6 h |
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| Formula | C8H11NO |
| Molar mass | 137.182 g·mol−1 |
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| Melting point | 170 to 172 °C (338 to 342 °F) [1] |
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Emoxypine (2-ethyl-6-methyl-3-hydroxypyridine), also known as Mexidol or Mexifin when used as the succinate salt, is an antioxidant actoprotector manufactured by Pharmasoft Pharmaceuticals.[2][3] Its chemical structure resembles that of pyridoxine (a type of vitamin B6).
History
Emoxypine was first synthesized by L.D. Smirnov and K.M. Dumayev, then studied and developed in the Institute of Pharmacology, Russian Academy of Medical Sciences and National Scientific Center of Bioactive Substances Safety.[4]
Use
Emoxypine has a wide range of applications in medical practice, primarily as anti-oxidant. It purportedly exercises anxiolytic,[5][6] anti-stress, anti-alcohol, anticonvulsant, nootropic, neuroprotective and anti-inflammatory action.[citation needed] Emoxypine presumably improves cerebral blood circulation, inhibits thrombocyte aggregation, lowers cholesterol levels, has cardioprotective and antiatherosclerotic action.[4] Compound's iron chelating property in vitro, shows potential in the management of neurodegenerative conditions such as Alzheimer's disease (AD), as well as hematologic disorders.[7]
Mechanism of action
Emoxypine's mechanism of action is believed to be its antioxidant and membrane-protective effects with the following key components:[4][8]
- Emoxypine inhibits oxidation of biomembrane lipids.
- Increases the activity of antioxidant enzymes, specifically that of superoxide dismutase, responsible for the formation and consumption of lipid peroxides and active oxygen forms.
- Inhibits free radicals during the synthesis of prostaglandin catalyzed cyclooxygenase and lipoxygenase, increases the correlation prostacyclin/ thromboxane A2 and blocks the leukotriene formation.
- Increases the content of polar fraction of lipids (phosphatidyl serine and phosphatidyl inositol) and reduces the cholesterol/phospholipids ratio which proves its lipid-regulatory properties; shifts structure transition into the low temperature zones, that is provokes the reduction of membrane viscosity and the increase of its fluidity, increases lipid-protein ratio.
- Modulates the activity of membrane-bound enzymes: phosphodiesterase, cyclic nucleotides, adenylate cyclase, aldoreductase, acetylcholinesterase.
- Modulates the receptor complexes of the brain membranes, i.e. benzodiazepine, GABA, acetylcholine receptors by increasing their binding ability.
- Stabilizes biomembranes, i.e. membrane structures of blood cells - erythrocytes and thrombocytes during their haemolysis or mechanical injury accompanied by the formation of free radicals.
- Changes the monoamine level and increases the dopamine content in the brain.[4][9]
Clinical study
One study determined the effectiveness of emoxypine in 205 patients with clinical manifestations of lumbosacral radiculopathy (LSR). Patients were divided into two groups, and further were divided into subgroups depending on the presence of motor disturbances. All patients received a course of conventional medical treatment and physiotherapy; main group additionally received emoxypine. Thereafter, clinical-neurological control of long-term results of treatment in subgroups of patients was performed. The results showed that the use of emoxypine in the combined therapy of patients with LSR led to significant and persistent reduction of severity of pain syndrome and rapid recovery of function of spinal roots and peripheral nerves compared with conventional therapy.[4][10]
References
- ↑ "Synthesis of 3-Hydroxy-2-alkylpyridines". Canadian Journal of Chemistry 31 (6): 564–568. 1953. doi:10.1139/v53-079.
- ↑ "mexidol.ru, Pharmasoft Website". http://www.mexidol.ru/en.
- ↑ "Механізми актопротекторної дії похідних янтарної кислоти" (in uk). Лікарська справа (3): 78–85. 2013. PMID 25016753. https://liksprava.com/index.php/journal/issue/view/15/3-2013-FULL-PDF.
- ↑ 4.0 4.1 4.2 4.3 4.4 "ANTIOXIDANT MEXIDOL. The main neuropsychotropic effects and the mechanism of action". Institute of Pharmacology. Moscow, Russia: Russian Academy of Medical Sciences. http://www.mexidol.ru/en/pro/library/farmacology/item102573.
- ↑ "Comparative analysis of the anxiolytic effects of 3-hydroxypyridine and succinic acid derivatives". Bulletin of Experimental Biology and Medicine 158 (6): 756–61. April 2015. doi:10.1007/s10517-015-2855-3. PMID 25894772.
- ↑ "Antioxidant Treatment of Ischemic Brain Lesions". Neuroscience and Behavioral Physiology 42 (8): 842–845. October 2012. doi:10.1007/s11055-012-9646-3.
- ↑ "Promising effects of emoxypine and its succinate derivative in the management of various diseases-with insights on recent patent applications". Current Research in Pharmacology and Drug Discovery 3: 100121. 2022. doi:10.1016/j.crphar.2022.100121. PMID 35992374.
- ↑ Antioxidants in the prophylaxis and therapy of CNS pathologies. (Report). Moscow. 1995.[page needed]
- ↑ "[Mexidol potentiates antiparkinsonian effect of L-DOPA in MPTP-induced parkinsonism model]". Eksperimental'naia i Klinicheskaia Farmakologiia 64 (1): 22–5. January 2001. PMID 11544797.
- ↑ "[Clinical and immunological assessment of efficacy of mexidol in the treatment of lumbosacral radiculopathy]". Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova 106 (10): 52–7. 2006. PMID 17117675.
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