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    CAS 13258-59-8

    BUILDING BLOCK

    PharmaCompass
    Xls

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    2D Structure
    Also known as: 13258-59-8, 2-ethyl-6-methylpyridin-3-ol hydrochloride, Emoxipin hydrochloride, 2-ethyl-6-methyl-3-pyridinol hydrochloride, 2-ethyl-3-hydroxy-6-methylpyridine hcl, 3-pyridinol, 2-ethyl-6-methyl-, hydrochloride
    Molecular Formula
    C8H12ClNO
    Molecular Weight
    173.64  g/mol
    InChI Key
    KZUIXWYHQJZUOK-UHFFFAOYSA-N
    FDA UNII
    SN1FWZ77AE
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    2-ethyl-6-methylpyridin-3-ol;hydrochloride
    2.1.2 InChI
    InChI=1S/C8H11NO.ClH/c1-3-7-8(10)5-4-6(2)9-7;/h4-5,10H,3H2,1-2H3;1H
    2.1.3 InChI Key
    KZUIXWYHQJZUOK-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CCC1=C(C=CC(=N1)C)O.Cl
    2.2 Other Identifiers
    2.2.1 UNII
    SN1FWZ77AE
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. 2-ethyl-6-methyl-3-hydroxypyridine

    2. 2-ethyl-6-methyl-3-oxypyridine

    3. 6-methyl-2-ethyl-3-hydroxypyridine

    4. 6-methyl-2-ethyl-3-hydroxypyridine Hydrochloride

    5. 6-methyl-2-ethyl-3-hydroxypyridine Monohydrochloride

    6. Emoxipin

    7. Emoxipine

    8. Emoxypin

    9. Emoxypine

    10. Epigid

    11. Hydroxypyridine-6

    2.3.2 Depositor-Supplied Synonyms

    1. 13258-59-8

    2. 2-ethyl-6-methylpyridin-3-ol Hydrochloride

    3. Emoxipin Hydrochloride

    4. 2-ethyl-6-methyl-3-pyridinol Hydrochloride

    5. 2-ethyl-3-hydroxy-6-methylpyridine Hcl

    6. 3-pyridinol, 2-ethyl-6-methyl-, Hydrochloride

    7. Emoxypine Hydrochloride

    8. 2-ethyl-3-hydroxy-6-methylpyridine Hydrochloride

    9. Sn1fwz77ae

    10. 2-ethyl-6-methylpyridin-3-ol;hydrochloride

    11. Hydroxypyridine-6

    12. 3-pyridinol, 2-ethyl-6-methyl-, Hydrochloride (1:1)

    13. Sd 6 (antioxidant)

    14. Op 6 (pharmaceutical)

    15. Emoxipin Hcl

    16. Mexidol Hydrochloride

    17. Unii-sn1fwz77ae

    18. Emoxypin Hydrochloride

    19. Op-6

    20. Schembl1373708

    21. Dtxsid80157647

    22. Bcp13397

    23. Ck1206

    24. Mfcd00460776

    25. Akos005267199

    26. Methylethylpiridinol Hydrochloride

    27. Ds-15704

    28. 2-ethyl-6-methylpyridin-3-olhydrochloride

    29. Db-002447

    30. Cs-0061447

    31. Ft-0612241

    32. 258e598

    33. Methylethylpiridinol Hydrochloride [who-dd]

    34. Q27289297

    35. 3-hydroxy-6-methyl-2-ethylpyridine Hydrochloride

    2.4 Create Date
    2005-08-08
    3 Chemical and Physical Properties
    Molecular Weight 173.64 g/mol
    Molecular Formula C8H12ClNO
    Hydrogen Bond Donor Count2
    Hydrogen Bond Acceptor Count2
    Rotatable Bond Count1
    Exact Mass173.0607417 g/mol
    Monoisotopic Mass173.0607417 g/mol
    Topological Polar Surface Area33.1 Ų
    Heavy Atom Count11
    Formal Charge0
    Complexity105
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count2
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Psychotropic Drugs

    A loosely defined grouping of drugs that have effects on psychological function. Here the psychotropic agents include the antidepressive agents, hallucinogens, and tranquilizing agents (including the antipsychotics and anti-anxiety agents). (See all compounds classified as Psychotropic Drugs.)

    Radiation-Protective Agents

    Drugs used to protect against ionizing radiation. They are usually of interest for use in radiation therapy but have been considered for other purposes, e.g. military. (See all compounds classified as Radiation-Protective Agents.)

    Mutagens

    Chemical agents that increase the rate of genetic mutation by interfering with the function of nucleic acids. A clastogen is a specific mutagen that causes breaks in chromosomes. (See all compounds classified as Mutagens.)

    Antioxidants

    Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)

    Anti-Arrhythmia Agents

    Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade. (See all compounds classified as Anti-Arrhythmia Agents.)

    Platelet Aggregation Inhibitors

    Drugs or agents which antagonize or impair any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system. (See all compounds classified as Platelet Aggregation Inhibitors.)