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    Betahistine Mesylate

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

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    2D Structure
    Also known as: Betahistine mesylate, 54856-23-4, Meginalisk, Merislon, Extovyl, Melopat
    Molecular Formula
    C10H20N2O6S2
    Molecular Weight
    328.4  g/mol
    InChI Key
    ZBJJDYGJCNTNTH-UHFFFAOYSA-N
    FDA UNII
    X1L0E3R43Y
    A histamine analog and H1 receptor agonist that serves as a vasodilator. It is used in MENIERE DISEASE and in vascular headaches but may exacerbate bronchial asthma and peptic ulcers.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    methanesulfonic acid;N-methyl-2-pyridin-2-ylethanamine
    2.1.2 InChI
    InChI=1S/C8H12N2.2CH4O3S/c1-9-7-5-8-4-2-3-6-10-8;2*1-5(2,3)4/h2-4,6,9H,5,7H2,1H3;2*1H3,(H,2,3,4)
    2.1.3 InChI Key
    ZBJJDYGJCNTNTH-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CNCCC1=CC=CC=N1.CS(=O)(=O)O.CS(=O)(=O)O
    2.2 Other Identifiers
    2.2.1 UNII
    X1L0E3R43Y
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Aequamen

    2. Betahistin Al

    3. Betahistin Ratiopharm

    4. Betahistin Stada

    5. Betahistin-ratiopharm

    6. Betahistine

    7. Betahistine Biphar

    8. Betahistine Dihydrobromide

    9. Betahistine Dihydrochloride

    10. Betahistine Hydrochloride

    11. Betahistine Mesylate

    12. Betahistine Methanesulfonate

    13. Betahistine Methanesulphonate

    14. Betaserc

    15. Betavert

    16. By Vertin

    17. By-vertin

    18. Dihydrobromide, Betahistine

    19. Dihydrochloride, Betahistine

    20. Extovyl

    21. Fidium

    22. Hydrochloride, Betahistine

    23. Lectil

    24. Melopat

    25. Mersilon

    26. Mesylate, Betahistine

    27. Methanesulfonate, Betahistine

    28. Methanesulphonate, Betahistine

    29. Pt 9

    30. Pt-9

    31. Pt9

    32. Ribrain

    33. Serc

    34. Vasomotal

    35. Vertigon

    2.3.2 Depositor-Supplied Synonyms

    1. Betahistine Mesylate

    2. 54856-23-4

    3. Meginalisk

    4. Merislon

    5. Extovyl

    6. Melopat

    7. 2-pyridineethanamine, N-methyl-, Dimethanesulfonate

    8. Tenyl

    9. Betahistine Methanesulfonate

    10. Betahistine Dimesylate

    11. Betahistine (mesylate)

    12. Methanesulfonic Acid;n-methyl-2-pyridin-2-ylethanamine

    13. X1l0e3r43y

    14. 2-[2-(methylamino)ethyl]pyridine Methanesulfonate

    15. Riptonin

    16. Einecs 259-377-7

    17. Unii-x1l0e3r43y

    18. Tenoxican

    19. Suzutolon (tn)

    20. 2-(ethylammonio)-n-methylpyridinium Dimethanesulphonate

    21. Betahistine Dimethanesulfonate

    22. Betahistine Mesilate (jp17)

    23. Betahistine Di Mesylate

    24. Schembl194604

    25. Chembl4303472

    26. Chebi:31274

    27. Hms2096n07

    28. Hms3713n07

    29. Hms3886k08

    30. Bcp13129

    31. Hy-d0237

    32. Betahistine Mesilate [mart.]

    33. Mfcd00211321

    34. S5498

    35. Betahistine Mesilate [who-dd]

    36. Akos015898737

    37. Ccg-220543

    38. Ac-23916

    39. Betahistine Mesilate [ep Impurity]

    40. Betahistine Mesilate [ep Monograph]

    41. Db-052657

    42. Cs-0010146

    43. Ft-0622912

    44. D01592

    45. D87714

    46. N-methyl-2-pyridineethylamine Dimethanesulfonate

    47. Bethahistinemethanesulfonate;betahistine Mesilate

    48. N-methyl-2-(2-pyridinyl)ethanamine Methanesulfonate

    49. Sr-01000722006-3

    50. W-105601

    51. Q27293318

    52. N-methyl-2-(pyridin-2-yl)ethanamine Dimethanesulfonate

    53. 2-pyridineethanamine, N-methyl-, Dimethanesulphonate

    54. N-methyl-2-(pyridin-2-yl)ethan-1-amine Dimethanesulfonate

    55. 2-pyridineethanamine, N-methyl-, Methanesulfonate (1:2)

    56. 2-pyridineethanamine, N-methyl-, Methanesulphonate (1:2)

    2.4 Create Date
    2005-06-24
    3 Chemical and Physical Properties
    Molecular Weight 328.4 g/mol
    Molecular Formula C10H20N2O6S2
    Hydrogen Bond Donor Count3
    Hydrogen Bond Acceptor Count8
    Rotatable Bond Count3
    Exact Mass328.07627871 g/mol
    Monoisotopic Mass328.07627871 g/mol
    Topological Polar Surface Area150 Ų
    Heavy Atom Count20
    Formal Charge0
    Complexity176
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count3
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Histamine Agonists

    Drugs that bind to and activate histamine receptors. Although they have been suggested for a variety of clinical applications histamine agonists have so far been more widely used in research than therapeutically. (See all compounds classified as Histamine Agonists.)

    Vasodilator Agents

    Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)