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    Triprolidine Hydrochloride

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    2D Structure
    Also known as: 550-70-9, Actidilat, Venen, Actidil, Trans-triprolidine hydrochloride, Pro-actidil
    Molecular Formula
    C19H23ClN2
    Molecular Weight
    314.9  g/mol
    InChI Key
    WYUYEJNGHIOFOC-NWBUNABESA-N
    FDA UNII
    NG7A104R3J
    Histamine H1 antagonist used in allergic rhinitis; ASTHMA; and URTICARIA. It is a component of COUGH and COLD medicines. It may cause drowsiness.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    2-[(E)-1-(4-methylphenyl)-3-pyrrolidin-1-ylprop-1-enyl]pyridine;hydrochloride
    2.1.2 InChI
    InChI=1S/C19H22N2.ClH/c1-16-7-9-17(10-8-16)18(19-6-2-3-12-20-19)11-15-21-13-4-5-14-21;/h2-3,6-12H,4-5,13-15H2,1H3;1H/b18-11+;
    2.1.3 InChI Key
    WYUYEJNGHIOFOC-NWBUNABESA-N
    2.1.4 Canonical SMILES
    CC1=CC=C(C=C1)C(=CCN2CCCC2)C3=CC=CC=N3.Cl
    2.1.5 Isomeric SMILES
    CC1=CC=C(C=C1)/C(=C\CN2CCCC2)/C3=CC=CC=N3.Cl
    2.2 Other Identifiers
    2.2.1 UNII
    NG7A104R3J
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Actidil

    2. Anhydrous, Triprolidine Hydrochloride

    3. Hydrochloride Anhydrous, Triprolidine

    4. Hydrochloride, Triprolidine

    5. Pro Actidil

    6. Triprolidine

    7. Triprolidine Hydrochloride Anhydrous

    8. Triprolidine Monohydrochloride

    9. Triprolidine Monohydrochloride, (z)-isomer

    10. Triprolidine Monohydrochloride, Monohydrate

    11. Triprolidine Oxalate

    12. Triprolidine Oxalate, (trans)-isomer

    13. Triprolidine, (z)-isomer

    2.3.2 Depositor-Supplied Synonyms

    1. 550-70-9

    2. Actidilat

    3. Venen

    4. Actidil

    5. Trans-triprolidine Hydrochloride

    6. Pro-actidil

    7. Pro-entra

    8. Triprolidine Hydrochloride Anhydrous

    9. 6138-79-0

    10. Entra

    11. (e)-2-(3-(pyrrolidin-1-yl)-1-(p-tolyl)prop-1-en-1-yl)pyridine Hydrochloride

    12. Triprolidine Hydrochloride (anhydrous)

    13. Mls000028751

    14. Ng7a104r3j

    15. Chebi:84119

    16. Pyridine, 2-(1-(4-methylphenyl)-3-(1-pyrrolidinyl)-1-propenyl)-, Monohydrochloride, (e)-

    17. Smr000058521

    18. Triprolidine (hydrochloride)

    19. Triprolidine Hydrochloride (anh.)

    20. Sr-01000075292

    21. Einecs 208-985-0

    22. Unii-ng7a104r3j

    23. Pyridine, 2-((1e)-1-(4-methylphenyl)-3-(1-pyrrolidinyl)-1-propenyl)-, Monohydrochloride

    24. Prestwick_575

    25. Mfcd00039044

    26. Opera_id_1214

    27. (e)-2-[3-(1-pyrrolidinyl)-1-p-tolylpropenyl]pyridine Hydrochloride

    28. Trans-2-(3-(1-pyrrolidinyl)-1-p-tolylpropenyl)pyridine Monohydrochloride

    29. Schembl42145

    30. Mls001148254

    31. Mls002207213

    32. Mls002222226

    33. Spectrum1500598

    34. Chembl1200450

    35. Hy-b1808a

    36. Dtxsid10872513

    37. Hms1568f06

    38. Hms1921i07

    39. Hms3411o04

    40. Hms3675o04

    41. Pharmakon1600-01500598

    42. Triprolidine Hydrochloride, >=99%

    43. Tox21_501130

    44. Ccg-40331

    45. Nsc757361

    46. Triprolidine Monohydrochloride (anh.)

    47. Akos015962154

    48. Lp01130

    49. Triprolidine Monohydrochloride Anhydrous

    50. Pyridine, 2-(3-(1-pyrrolidinyl)-1-p-tolylpropenyl)-, Monohydrochloride, (e)-

    51. Ncgc00094397-01

    52. Ncgc00094397-02

    53. Ncgc00094397-03

    54. Ncgc00261815-01

    55. Ac-15905

    56. As-13971

    57. Triprolidine Monohydrochloride (anhydrous)

    58. Anhydrous Triprolidine Hydrochloride

    59. Triprolidine Hydrochloride [who-dd]

    60. Cs-0013855

    61. Eu-0101130

    62. T 6764

    63. 138t790

    64. A868718

    65. A923663

    66. Anhydrous Triprolidine Hydrochloride [mart.]

    67. Sr-01000075292-1

    68. Sr-01000075292-3

    69. Sr-01000075292-7

    70. Triprolidine Hydrochloride, Sigma Reference Standard

    71. Q27157492

    72. (e)-2-(3-(1-pyrrolidinyl)-1-p-tolylpropenyl)pyridine Monohydrochloride

    73. (e)-2-(3-(pyrrolidin-1-yl)-1-(p-tolyl)prop-1-en-1-yl)pyridinehydrochloride

    74. (e)-2-[1-(4-methylphenyl)-3-(1-pyrrolidinyl)-1-propenyl]pyridine Hydrochloride

    75. 1-[(2e)-3-(4-methylphenyl)-3-(pyridin-2-yl)prop-2-en-1-yl]pyrrolidinium Chloride

    76. 2-[(1e)-1-(4-methylphenyl)-3-(pyrrolidin-1-yl)prop-1-en-1-yl]pyridine Hydrochloride

    2.4 Create Date
    2006-03-07
    3 Chemical and Physical Properties
    Molecular Weight 314.9 g/mol
    Molecular Formula C19H23ClN2
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count2
    Rotatable Bond Count4
    Exact Mass314.1549764 g/mol
    Monoisotopic Mass314.1549764 g/mol
    Topological Polar Surface Area16.1 Ų
    Heavy Atom Count22
    Formal Charge0
    Complexity336
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count1
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count2
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Histamine H1 Antagonists

    Drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine. Included here are the classical antihistaminics that antagonize or prevent the action of histamine mainly in immediate hypersensitivity. They act in the bronchi, capillaries, and some other smooth muscles, and are used to prevent or allay motion sickness, seasonal rhinitis, and allergic dermatitis and to induce somnolence. The effects of blocking central nervous system H1 receptors are not as well understood. (See all compounds classified as Histamine H1 Antagonists.)

    Anti-Allergic Agents

    Agents that are used to treat allergic reactions. Most of these drugs act by preventing the release of inflammatory mediators or inhibiting the actions of released mediators on their target cells. (From AMA Drug Evaluations Annual, 1994, p475) (See all compounds classified as Anti-Allergic Agents.)