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emoxypine

Structure via PubChem · Public domain (PubChem)

EntityQ4532982· pop 5· linked from 7 articles

Emoxypine (2-ethyl-6-methyl-3-hydroxypyridine), also known as Mexidol or Mexifin, a succinate salt, is chemical compound which is claimed by its manufacturer, the Russian company Pharmasoft Pharmaceuticals, to have antioxidant and actoprotector properties, but these purported properties of emoxypine have not been proven. Its chemical structure resembles that of pyridoxine (a type of vitamin B6).

Chemical data

Formula
C8H11NO
Molecular weight
137.18 g/mol
IUPAC name
2-ethyl-6-methylpyridin-3-ol
SMILES
CCC1=C(C=CC(=N1)C)O
InChIKey
JPGDYIGSCHWQCC-UHFFFAOYSA-N
XLogP
1.7
Polar surface area
33.1 Ų
H-bond donors
1
H-bond acceptors
2
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 3
Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Has part
carbon
Mass
137.084
Show 5 more facts
chemical formula
C₈H₁₁NO
canonical SMILES
CCC1=C(C=CC(=N1)C)O
subject has role
nootropic
different from
amoxapine
Commons category
Emoxypine
Sources (3)

via Wikidata · CC0

~4 min read

Encyclopedic overview

8 sections
Contents
  • History
  • Use
  • Mechanism of action
  • Clinical study
  • Legal status
  • See also
  • References
  • External links

Emoxypine (2-ethyl-6-methyl-3-hydroxypyridine), also known as Mexidol or Mexifin, a succinate salt, is chemical compound which is claimed by its manufacturer, the Russian company Pharmasoft Pharmaceuticals, to have antioxidant and actoprotector properties, but these purported properties of emoxypine have not been proven. 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 Russian Institute of Pharmacology, Russian Academy of Medical Sciences and Russian Scientific Center of Bioactive Substances Safety. Its research and use has been largely isolated to former soviet states, with little interest from other countries.

Excerpted from Wikipedia’s “emoxypine” article, available under the CC BY-SA 4.0 licence.

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