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    Propiverine Hydrochloride

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    2D Structure
    Also known as: Propiverine hydrochloride, 54556-98-8, Mictonetten, Propiverine (hydrochloride), Propiverine hcl, 1-methyl-4-piperidyl diphenylpropoxyacetate hydrochloride
    Molecular Formula
    C23H30ClNO3
    Molecular Weight
    403.9  g/mol
    InChI Key
    KFUJMHHNLGCTIJ-UHFFFAOYSA-N
    FDA UNII
    DC4GZD10H3
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    (1-methylpiperidin-4-yl) 2,2-diphenyl-2-propoxyacetate;hydrochloride
    2.1.2 InChI
    InChI=1S/C23H29NO3.ClH/c1-3-18-26-23(19-10-6-4-7-11-19,20-12-8-5-9-13-20)22(25)27-21-14-16-24(2)17-15-21;/h4-13,21H,3,14-18H2,1-2H3;1H
    2.1.3 InChI Key
    KFUJMHHNLGCTIJ-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CCCOC(C1=CC=CC=C1)(C2=CC=CC=C2)C(=O)OC3CCN(CC3)C.Cl
    2.2 Other Identifiers
    2.2.1 UNII
    DC4GZD10H3
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Alpha-diphenyl Alpha-n-propoxyacetic Acid-4(1-methylpiperidyl)ester

    2. Detrunorm

    3. Mictonetten

    4. Propiverin

    5. Propiverine

    6. Propiverine Hydrochloride

    2.3.2 Depositor-Supplied Synonyms

    1. Propiverine Hydrochloride

    2. 54556-98-8

    3. Mictonetten

    4. Propiverine (hydrochloride)

    5. Propiverine Hcl

    6. 1-methyl-4-piperidyl Diphenylpropoxyacetate Hydrochloride

    7. Nsc-172140

    8. Propiverine Hydrochloride [jan]

    9. (1-methylpiperidin-4-yl) 2,2-diphenyl-2-propoxyacetate;hydrochloride

    10. Dsstox_cid_26847

    11. Dsstox_rid_81957

    12. Dsstox_gsid_46847

    13. Detrunorm

    14. Dc4gzd10h3

    15. Cas-54556-98-8

    16. Ncgc00181103-01

    17. P-4

    18. Mictonorm (tn)

    19. Propiverin Hydrochloride

    20. (1-methylpiperidin-4-yl) 2,2-diphenyl-2-propoxyacetate Hydrochloride

    21. Bup-4 (tn)

    22. Chebi:8494

    23. Schembl1034248

    24. Chembl2359059

    25. Dtxsid1046847

    26. Propiverine Hydrochloride (jp17)

    27. Bcp09576

    28. Tox21_112719

    29. Nsc172140

    30. S4931

    31. Propiverine Hydrochloride [mi]

    32. Akos015962920

    33. Tox21_112719_1

    34. Ac-2076

    35. Ac-8718

    36. Ccg-268683

    37. Hy-116408a

    38. Ncgc00181103-02

    39. Propiverine Hydrochloride [who-dd]

    40. Db-015754

    41. Cs-0091435

    42. Ft-0656926

    43. D01007

    44. Q27276325

    45. (1-methylpiperidin-4-yl)2,2-diphenyl-2-propoxyacetate Hydrochloride

    46. (1-methyl-3,4,5,6-tetrahydro-2h-pyridin-4-yl)2,2-diphenyl-2-propoxy Acetate Hcl

    47. (1-methyl-3,4,5,6-tetrahydro-2h-pyridin-4-yl) 2,2-diphenyl-2-propoxy Acetate Hydrochloride

    2.4 Create Date
    2005-06-24
    3 Chemical and Physical Properties
    Molecular Weight 403.9 g/mol
    Molecular Formula C23H30ClNO3
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count4
    Rotatable Bond Count8
    Exact Mass403.1914215 g/mol
    Monoisotopic Mass403.1914215 g/mol
    Topological Polar Surface Area38.8 Ų
    Heavy Atom Count28
    Formal Charge0
    Complexity429
    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

    Urological Agents

    Drugs used in the treatment of urological conditions and diseases such as URINARY INCONTINENCE and URINARY TRACT INFECTIONS. (See all compounds classified as Urological Agents.)

    Muscarinic Antagonists

    Drugs that bind to but do not activate MUSCARINIC RECEPTORS, thereby blocking the actions of endogenous ACETYLCHOLINE or exogenous agonists. Muscarinic antagonists have widespread effects including actions on the iris and ciliary muscle of the eye, the heart and blood vessels, secretions of the respiratory tract, GI system, and salivary glands, GI motility, urinary bladder tone, and the central nervous system. (See all compounds classified as Muscarinic Antagonists.)

    Parasympatholytics

    Agents that inhibit the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the MUSCARINIC ANTAGONISTS. (See all compounds classified as Parasympatholytics.)