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Technical details about Isothipendyl Hydrochloride, learn more about the structure, uses, toxicity, action, side effects and more

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2D Structure
Also known as: 1225-60-1, Andantol, Theruhistin, Adantol, Isothipendyl hcl, Isothipendyl monohydrochloride
Molecular Formula
C16H20ClN3S
Molecular Weight
321.9  g/mol
InChI Key
RQHCFTORMXCNGP-UHFFFAOYSA-N
FDA UNII
953AP1LBV8

1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
N,N-dimethyl-1-pyrido[3,2-b][1,4]benzothiazin-10-ylpropan-2-amine;hydrochloride
2.1.2 InChI
InChI=1S/C16H19N3S.ClH/c1-12(18(2)3)11-19-13-7-4-5-8-14(13)20-15-9-6-10-17-16(15)19;/h4-10,12H,11H2,1-3H3;1H
2.1.3 InChI Key
RQHCFTORMXCNGP-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CC(CN1C2=CC=CC=C2SC3=C1N=CC=C3)N(C)C.Cl
2.2 Other Identifiers
2.2.1 UNII
953AP1LBV8
2.3 Synonyms
2.3.1 MeSH Synonyms

1. 10-(2-dimethylamino-2-methylethyl)-10h-pyrido(3,2- B)(1,4)benzothiazine

2. Andantol

3. Andanton

4. Estamyl

5. Isothipendyl

6. Sedermyl

2.3.2 Depositor-Supplied Synonyms

1. 1225-60-1

2. Andantol

3. Theruhistin

4. Adantol

5. Isothipendyl Hcl

6. Isothipendyl Monohydrochloride

7. Isothipendyl Hydrochloride [jan]

8. Andanton

9. Nilergex

10. Nsc 169186

11. Nsc-169186

12. Isothipendyl (hydrochloride)

13. 10-(2-dimethylaminopropyl)-10h-pyrido(3,2-b)(1,4)benzothiazine Hydrochloride

14. 953ap1lbv8

15. N-dimethylaminoisopropylthiophenylpyridylamine Hydrochloride

16. 34433-15-3

17. Nsc169186

18. (+/-)-isothipendyl Hydrochloride

19. 10h-pyrido(3,2-b)(1,4)benzothiazine-10-ethanamine, N,n,2-trimethyl-, Monohydrochloride

20. N,n-dimethyl-1-pyrido[3,2-b][1,4]benzothiazin-10-ylpropan-2-amine;hydrochloride

21. Adanton Hydrochloride

22. Udantol Hydrochloride

23. Nilergex Hydrochloride

24. Isothipendyl Hydrochloride (jan)

25. Theruhistin Hydrochloride

26. Einecs 214-957-9

27. Unii-953ap1lbv8

28. Andantol (tn)

29. Einecs 252-022-7

30. 10-(2-dimethylaminopropyl)-1-azaphenothiazine Hydrochloride

31. Dimethylamino-isopropyl-thiophenyl-pyridylamin Hydrochlorid [german]

32. Ncgc00181101-01

33. 10-(2-dimethylaminopropyl)-(1)-4-azaphenthiazin Hydrochlorid [german]

34. 10-(2-dimethylaminopropyl)-9-thia-1,10-diazaanthracene Hydrochloride

35. 10-(2-dimethylamino-2-methylethyl)-10h-pyrido(3,2-b)(1,4)benzothiazine Hydrochloride

36. 10h-pyrido(3,2-b)(1,4)benzothiazine, 10-(2-(dimethylamino)propyl)-, Monohydrochloride

37. Dsstox_cid_26845

38. Dsstox_rid_81955

39. Dsstox_gsid_46845

40. Schembl230214

41. Chembl2107246

42. Dtxsid1046845

43. Chebi:31734

44. Dimethylamino-isopropyl-thiophenyl-pyridylamin Hydrochlorid

45. 10-(2-dimethylaminopropyl)-(1)-4-azaphenthiazin Hydrochlorid

46. Tox21_112717

47. Isothipendyl Hydrochloride [mi]

48. 10-(2-(dimethylamino)propyl)-10h-pyrido(3,2-b)(1,4)benzothiazine Hydrochloride

49. 10h-pyrido(3,2-b)(1,4)benzothiazine, 10-(2-dimethylamino-2-methylethyl)-, Hydrochloride

50. Isothipendyl Hydrochloride [mart.]

51. Cas-1225-60-1

52. Isothipendyl Hydrochloride [who-dd]

53. Ft-0700699

54. Isothipendyl Hydrochloride, (+/-)-

55. D01143

56. Q27271733

57. 10h-pyrido[3,4]benzothiazine, 10-(2-dimethylamino-2-methylethyl)-, Hydrochloride

58. 10h-pyrido[3,4]benzothiazine, 10-[2-(dimethylamino)propyl]-, Monohydrochloride

59. 10h-pyrido[3,4]benzothiazine-10-ethanamine, N,n,2-trimethyl-, Monohydrochloride

60. N,n,alpha-trimethyl-10h-pyrido[3,2-b][1,4]benzothiazine-10-ethanamine Hydrochloride

2.4 Create Date
2005-06-24
3 Chemical and Physical Properties
Molecular Weight 321.9 g/mol
Molecular Formula C16H20ClN3S
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass321.1066465 g/mol
Monoisotopic Mass321.1066465 g/mol
Topological Polar Surface Area44.7 Ų
Heavy Atom Count21
Formal Charge0
Complexity323
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Histamine Antagonists

Drugs that bind to but do not activate histamine receptors, thereby blocking the actions of histamine or histamine agonists. Classical antihistaminics block the histamine H1 receptors only. (See all compounds classified as Histamine Antagonists.)