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    Phenidone

    ACTIVE PHARMA INGREDIENTS

    PharmaCompass
    $ API Ref.Price (USD/KG) : 26Xls

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    2D Structure
    Also known as: 92-43-3, 1-phenylpyrazolidin-3-one, 1-phenyl-3-pyrazolidinone, 1-phenyl-3-pyrazolidone, Fenidon, 3-pyrazolidinone, 1-phenyl-
    Molecular Formula
    C9H10N2O
    Molecular Weight
    162.19  g/mol
    InChI Key
    CMCWWLVWPDLCRM-UHFFFAOYSA-N
    FDA UNII
    H0U5612P6K
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    1-phenylpyrazolidin-3-one
    2.1.2 InChI
    InChI=1S/C9H10N2O/c12-9-6-7-11(10-9)8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,12)
    2.1.3 InChI Key
    CMCWWLVWPDLCRM-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    C1CN(NC1=O)C2=CC=CC=C2
    2.2 Other Identifiers
    2.2.1 UNII
    H0U5612P6K
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Phenidone Monohydrochloride

    2.3.2 Depositor-Supplied Synonyms

    1. 92-43-3

    2. 1-phenylpyrazolidin-3-one

    3. 1-phenyl-3-pyrazolidinone

    4. 1-phenyl-3-pyrazolidone

    5. Fenidon

    6. 3-pyrazolidinone, 1-phenyl-

    7. Pyrazolidinone, 1-phenyl-

    8. 1-phenyl-3-oxopyrazolidine

    9. 2-pyrazolin-3-ol, 1-phenyl-

    10. 1-p-3-p

    11. 1-phenyl-pyrazolidin-3-one

    12. 1-phenylpyrazolid-3-one

    13. Chembl7660

    14. 1-phenyl-4,5-dihydro-1h-pyrazol-3-ol

    15. Mls002639322

    16. H0u5612p6k

    17. Nsc-30306

    18. Ccris 3624

    19. Einecs 202-155-1

    20. 3-pyrazolidinone,1-phenyl-

    21. Unii-h0u5612p6k

    22. Phenidone A

    23. Mfcd00003094

    24. Wln: T5nmvtj Ar

    25. N-phenylpyrazolidin-3-one

    26. Chemdiv3_006595

    27. Timtec1_001225

    28. Dsstox_cid_29393

    29. Dsstox_rid_83508

    30. 1-phenyl Pyrazolidine-3-one

    31. Dsstox_gsid_49433

    32. Oprea1_428400

    33. Schembl235192

    34. Schembl9670254

    35. Dtxsid1049433

    36. Schembl10371905

    37. 1-phenyl-3-pyrazolidinone, 97%

    38. Hms1491l17

    39. Hms1537h15

    40. Hms3091p11

    41. Hms3886e10

    42. Albb-010492

    43. Nsc30306

    44. Zinc2769764

    45. Tox21_202877

    46. 1-phenyltetrahydro-3h-pyrazol-3-one

    47. Bdbm50009004

    48. S5520

    49. Stk084358

    50. Stk741678

    51. Akos000119161

    52. Akos003264132

    53. (phenidone)1-phenyl-pyrazolidin-3-one

    54. 1-phenyl-pyrazolidin-3-one(phenidone)

    55. Ccg-207926

    56. Cs-w010860

    57. Fs-4504

    58. Hy-w010144

    59. Sdccgmls-0064787.p001

    60. Cas-92-43-3

    61. Idi1_024505

    62. 1-phenyl-3-pyrazolidinone [mi]

    63. 1-phenyl-pyrazolidin-3-one (phenidone)

    64. Ncgc00174656-01

    65. Ncgc00260423-01

    66. Smr001548767

    67. Db-057302

    68. Ft-0608244

    69. P0153

    70. D78316

    71. Sr-01000516084

    72. Q-200133

    73. Q3297749

    74. Sr-01000516084-1

    75. F0905-7615

    76. 14776-33-1

    2.4 Create Date
    2005-03-26
    3 Chemical and Physical Properties
    Molecular Weight 162.19 g/mol
    Molecular Formula C9H10N2O
    XLogP30.9
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count2
    Rotatable Bond Count1
    Exact Mass162.079312947 g/mol
    Monoisotopic Mass162.079312947 g/mol
    Topological Polar Surface Area32.3 Ų
    Heavy Atom Count12
    Formal Charge0
    Complexity175
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Cyclooxygenase Inhibitors

    Compounds or agents that combine with cyclooxygenase (PROSTAGLANDIN-ENDOPEROXIDE SYNTHASES) and thereby prevent its substrate-enzyme combination with arachidonic acid and the formation of eicosanoids, prostaglandins, and thromboxanes. (See all compounds classified as Cyclooxygenase Inhibitors.)

    Lipoxygenase Inhibitors

    Compounds that bind to and inhibit that enzymatic activity of LIPOXYGENASES. Included under this category are inhibitors that are specific for lipoxygenase subtypes and act to reduce the production of LEUKOTRIENES. (See all compounds classified as Lipoxygenase Inhibitors.)

    Antioxidants

    Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)