mexidol CAS 127464-43-1

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Model: MOS127464-43-1
Place of Origin: Sichuan,China (Mainland)
Brand: MOSINTER
CAS: 127464-43-1
Name: mexidol
Appearance: white powder
Alias: 2-Ethyl-6-Methyl-3-pyridinol butanoate
Molecular formula: C8H11NO.C4H6O4
Assay: 97%
Molecular weight: 255.268

mexidol (CAS: 127464-43-1)

Synonyms 2-Ethyl-6-methyl-3-pyridinol butanoate (1:1); 2-ethyl-6-methylpyridin-3-ol butanedioate (1:1)
Molecular Formula C12H17NO5
Molecular Weight 255.2671
InChI InChI=1/C8H11NO.C4H6O4/c1-3-7-8(10)5-4-6(2)9-7;5-3(6)1-2-4(7)8/h4-5,10H,3H2,1-2H3;1-2H2,(H,5,6)(H,7,8)
CAS Registry Number 127464-43-1
Molecular Structure
Boiling point 280.6°C at 760 mmHg
Flash point 123.5°C
Vapour Pressur 0.0022mmHg at 25°C

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.History

Use

In Russia, emoxypine has a wide range of applications in medical practice. It purportedly exercises anxiolytic, anti-stress, anti-alcohol,anticonvulsant, nootropic, neuroprotective and anti-inflammatory action. Emoxypine presumably improves cerebral blood circulation, inhibits thrombocyte aggregation, lowers cholesterol levels, has cardioprotective and antiatherosclerotic action.

Mechanism of action

Emoxypine’s mechanism of action is believed to be its antioxidant and membrane-protective effects with the following key components:

    • Emoxypine effectively inhibits free radical oxidation of biomembrane lipids, reacts to peroxide radicals of lipids primary and hydroxyl radical of peptides
    • 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 ration.
    • 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.
    • 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 lead 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.

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