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Technical details about Betahistine Mesylate, learn more about the structure, uses, toxicity, action, side effects and more

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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.)