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    Chemistry

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    Also known as: Benztropine mesylate, 132-17-2, Cogentin mesylate, Benztropine (mesylate), Mls000737056, Nsc42199
    Molecular Formula
    C22H29NO4S
    Molecular Weight
    403.5  g/mol
    InChI Key
    CPFJLLXFNPCTDW-UHFFFAOYSA-N
    Benztropine
    A centrally active muscarinic antagonist that has been used in the symptomatic treatment of PARKINSON DISEASE. Benztropine also inhibits the uptake of dopamine.
    1 2D Structure

    Benztropine

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    3-benzhydryloxy-8-methyl-8-azabicyclo[3.2.1]octane;methanesulfonic acid
    2.1.2 InChI
    InChI=1S/C21H25NO.CH4O3S/c1-22-18-12-13-19(22)15-20(14-18)23-21(16-8-4-2-5-9-16)17-10-6-3-7-11-17;1-5(2,3)4/h2-11,18-21H,12-15H2,1H3;1H3,(H,2,3,4)
    2.1.3 InChI Key
    CPFJLLXFNPCTDW-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CN1C2CCC1CC(C2)OC(C3=CC=CC=C3)C4=CC=CC=C4.CS(=O)(=O)O
    2.2 Synonyms
    2.2.1 MeSH Synonyms

    1. Apo Benztropine

    2. Apo-benztropine

    3. Bensylate

    4. Benzatropine

    5. Benzatropine Mesylate

    6. Benzatropine Methanesulfonate

    7. Benzatropine Methanesulfonate, Hydrobromide

    8. Benzatropine Methanesulfonate, Hydrobromide, (endo)-isomer

    9. Benzatropine Methanesulfonate, Hydrochloride, (endo)-isomer

    10. Benztropine

    11. Benztropine Mesylate

    12. Cogentin

    13. Cogentinol

    14. Hydrobromide Benzatropine Methanesulfonate

    15. Mesylate, Benzatropine

    16. Mesylate, Benztropine

    17. Methanesulfonate, Benzatropine

    18. Methanesulfonate, Hydrobromide Benzatropine

    19. N Methylbenztropine

    20. N-methylbenztropine

    21. Pms Benztropine

    22. Pms-benztropine

    2.2.2 Depositor-Supplied Synonyms

    1. Benztropine Mesylate

    2. 132-17-2

    3. Cogentin Mesylate

    4. Benztropine (mesylate)

    5. Mls000737056

    6. Nsc42199

    7. Benzotropine Mesylate

    8. 3-(benzhydryloxy)-8-methyl-8-azabicyclo[3.2.1]octane Methanesulfonate

    9. Smr000394012

    10. Cobrentin Methanesulfonate

    11. 3-benzhydryloxy-8-methyl-8-azabicyclo[3.2.1]octane;methanesulfonic Acid

    12. Mk 02

    13. Benzatropine Mesylate;benzotropine Mesylate;benztropine Methanesulfonate

    14. Tropine Benzohydryl Ether Methanesulfonate

    15. 102701-02-0

    16. Cogentin Methanesulfonate

    17. Sr-01000075303

    18. Benzotropine Methanesulfonate

    19. Nsc-42199

    20. Benzotropinemesylate

    21. Opera_id_1229

    22. Schembl41809

    23. Chembl85236

    24. Hy-b0520a

    25. Hms2747a15

    26. Hms3259p11

    27. Hms3260h09

    28. Hms3652k07

    29. Tox21_500194

    30. Nsc169913

    31. 3-(diphenylmethoxy)-8-methyl-8-azabicyclo[3.2.1]octane, Methanesulfonic Acid

    32. Akos008105137

    33. Ccg-221498

    34. Lp00194

    35. Nc00646

    36. Sb19689

    37. Ncgc00016118-02

    38. Ncgc00093670-01

    39. Ncgc00260879-01

    40. As-17846

    41. B5592

    42. Cs-0300867

    43. Eu-0100194

    44. En300-51031

    45. B 8262

    46. Wln: T56 A Antj A1 Goyr & R & Osw1

    47. Benzophenone-3,3'-4,4'-tetracarboxylic Dianhydrie

    48. Q-200693

    49. Sr-01000075303-1

    50. Sr-01000075303-5

    51. 8-azabicyclo[3.2.1]octane, Endo-, Methanesulfonate

    52. 1.alpha.h, 3.alpha.-(diphenylmethoxy)-, Methanesulfonate

    53. 3-(diphenylmethoxy)-8-methyl-8-azabicyclo[3.2.1]octane,methanesulfonicacid

    54. Benzhydryl 8-methyl-8-azabicyclo[3.2.1]oct-3-yl Ether Methanesulfonate

    2.3 Create Date
    2005-03-26
    3 Chemical and Physical Properties
    Molecular Weight 403.5 g/mol
    Molecular Formula C22H29NO4S
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count5
    Rotatable Bond Count4
    Exact Mass403.18172958 g/mol
    Monoisotopic Mass403.18172958 g/mol
    Topological Polar Surface Area75.2 Ų
    Heavy Atom Count28
    Formal Charge0
    Complexity433
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count2
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count2
    4 Drug and Medication Information
    4.1 Drug Information
    1 of 2  
    Drug NameBenztropine mesylate
    PubMed HealthBenztropine Mesylate (By mouth)
    Drug ClassesAntiparkinsonian
    Drug LabelBenztropine Mesylate is a synthetic compound containing structural features found in atropine and diphenhydramine.It is a crystalline white powder, very soluble in water, designated as 3-(Diphenylmethoxy)-1H, 5H-tropane methanesulfonate, with t...
    Active IngredientBenztropine mesylate
    Dosage FormInjectable; Tablet
    RouteInjection; Oral
    Strength1mg/ml; 0.5mg; 2mg; 1mg
    Market StatusPrescription
    CompanyCorepharma; Navinta; Fresenius Kabi Usa; Excellium; Vintage; Usl Pharma; Luitpold; Hikma Farmaceutica; Pliva; Invagen Pharms

    2 of 2  
    Drug NameBenztropine mesylate
    PubMed HealthBenztropine Mesylate (By mouth)
    Drug ClassesAntiparkinsonian
    Drug LabelBenztropine Mesylate is a synthetic compound containing structural features found in atropine and diphenhydramine.It is a crystalline white powder, very soluble in water, designated as 3-(Diphenylmethoxy)-1H, 5H-tropane methanesulfonate, with t...
    Active IngredientBenztropine mesylate
    Dosage FormInjectable; Tablet
    RouteInjection; Oral
    Strength1mg/ml; 0.5mg; 2mg; 1mg
    Market StatusPrescription
    CompanyCorepharma; Navinta; Fresenius Kabi Usa; Excellium; Vintage; Usl Pharma; Luitpold; Hikma Farmaceutica; Pliva; Invagen Pharms

    5 Pharmacology and Biochemistry
    5.1 MeSH Pharmacological Classification

    Dopamine Uptake Inhibitors

    Drugs that block the transport of DOPAMINE into axon terminals or into storage vesicles within terminals. Most of the ADRENERGIC UPTAKE INHIBITORS also inhibit dopamine uptake. (See all compounds classified as Dopamine Uptake Inhibitors.)

    Antiparkinson Agents

    Agents used in the treatment of Parkinson's disease. The most commonly used drugs act on the dopaminergic system in the striatum and basal ganglia or are centrally acting muscarinic antagonists. (See all compounds classified as Antiparkinson Agents.)

    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.)

    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.)

    5.2 FDA Pharmacological Classification
    5.2.1 Pharmacological Classes
    Antihistamine [EPC]; Cholinergic Antagonists [MoA]; Histamine Receptor Antagonists [MoA]; Anticholinergic [EPC]

    API Reference Price

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    11-Jun-2021
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