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    Eperisone Hydrochloride

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    $ API Ref.Price (USD/KG) : 68Xls

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    2D Structure
    Also known as: 56839-43-1, Eperisone hcl, Myonal, Mional, Empp, Eperisone, hcl
    Molecular Formula
    C17H26ClNO
    Molecular Weight
    295.8  g/mol
    InChI Key
    GTAXGNCCEYZRII-UHFFFAOYSA-N
    FDA UNII
    U38O8U7P6X
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    1-(4-ethylphenyl)-2-methyl-3-piperidin-1-ylpropan-1-one;hydrochloride
    2.1.2 InChI
    InChI=1S/C17H25NO.ClH/c1-3-15-7-9-16(10-8-15)17(19)14(2)13-18-11-5-4-6-12-18;/h7-10,14H,3-6,11-13H2,1-2H3;1H
    2.1.3 InChI Key
    GTAXGNCCEYZRII-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CCC1=CC=C(C=C1)C(=O)C(C)CN2CCCCC2.Cl
    2.2 Other Identifiers
    2.2.1 UNII
    U38O8U7P6X
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. (4'-ethyl-2-methyl-3-piperidino)propiophenone

    2. 4-empp

    3. E-0646

    4. Eperisone

    2.3.2 Depositor-Supplied Synonyms

    1. 56839-43-1

    2. Eperisone Hcl

    3. Myonal

    4. Mional

    5. Empp

    6. Eperisone, Hcl

    7. E-646

    8. 1-(4-ethylphenyl)-2-methyl-3-(piperidin-1-yl)propan-1-one Hydrochloride

    9. Eperisone Hydrochloride [jan]

    10. 4'-ethyl-2-methyl-3-piperidinopropiophenone Hydrochloride

    11. U38o8u7p6x

    12. 1-(4-ethylphenyl)-2-methyl-3-(1-piperidinyl)-1-propanone Hydrochloride

    13. 1-(4-ethylphenyl)-2-methyl-3-piperidin-1-ylpropan-1-one;hydrochloride

    14. Dsstox_cid_27822

    15. Dsstox_rid_82585

    16. Dsstox_gsid_47844

    17. Cas-56839-43-1

    18. Ncgc00167973-01

    19. (4'-ethyl-2-methyl-3-piperidino)propiophenone

    20. Unii-u38o8u7p6x

    21. E 0646

    22. Epenard (tn)

    23. 1-propanone, 1-(4-ethylphenyl)-2-methyl-3-(1-piperidinyl)-, Hydrochloride

    24. Eperisonehydrochloride

    25. Dw-1030

    26. Schembl218337

    27. Chembl2360601

    28. Dtxsid8047844

    29. Eperisone Hydrochloride (jp17)

    30. Chebi:31540

    31. Bcp11969

    32. Hy-b1901

    33. Propiophenone, 4'-ethyl-2-methyl-3-piperidino-, Hydrochloride

    34. Eperisone Hydrochloride [mi]

    35. Tox21_112599

    36. Mfcd00941459

    37. Akos015843965

    38. Tox21_112599_1

    39. Ccg-267425

    40. Eperisone Hydrochloride [mart.]

    41. Ks-5241

    42. Eperisone Hydrochloride [who-dd]

    43. Ncgc00167973-02

    44. Ac-15896

    45. Db-052975

    46. Cs-0013960

    47. E2000

    48. Ft-0602324

    49. S4877

    50. D01671

    51. D95097

    52. E-2000

    53. A831198

    54. Q27889924

    55. 1-(4-ethylphenyl)-2-methyl-3-(piperidin-1-yl)propan-1-onehydrochloride

    56. 1-(4-ethylphenyl)-2-methyl-3-(1-piperidyl)propan-1-one Hydrochloride;eperisone Hcl

    2.4 Create Date
    2005-06-24
    3 Chemical and Physical Properties
    Molecular Weight 295.8 g/mol
    Molecular Formula C17H26ClNO
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count2
    Rotatable Bond Count5
    Exact Mass295.1702921 g/mol
    Monoisotopic Mass295.1702921 g/mol
    Topological Polar Surface Area20.3 Ų
    Heavy Atom Count20
    Formal Charge0
    Complexity275
    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

    Anticonvulsants

    Drugs used to prevent SEIZURES or reduce their severity. (See all compounds classified as Anticonvulsants.)

    Vasodilator Agents

    Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)

    Calcium Channel Blockers

    A class of drugs that act by selective inhibition of calcium influx through cellular membranes. (See all compounds classified as Calcium Channel Blockers.)

    Muscle Relaxants, Central

    A heterogeneous group of drugs used to produce muscle relaxation, excepting the neuromuscular blocking agents. They have their primary clinical and therapeutic uses in the treatment of muscle spasm and immobility associated with strains, sprains, and injuries of the back and, to a lesser degree, injuries to the neck. They have been used also for the treatment of a variety of clinical conditions that have in common only the presence of skeletal muscle hyperactivity, for example, the muscle spasms that can occur in MULTIPLE SCLEROSIS. (From Smith and Reynard, Textbook of Pharmacology, 1991, p358) (See all compounds classified as Muscle Relaxants, Central.)

    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.)