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    Flurbiprofen Axetil

    ACTIVE PHARMA INGREDIENTS

    PharmaCompass
    Xls

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    2D Structure
    Also known as: 91503-79-6, Ropion, Lfp 83, Fp 83, Fp-83, I0ou31pui5
    Molecular Formula
    C19H19FO4
    Molecular Weight
    330.3  g/mol
    InChI Key
    ALIVXCSEERJYHU-UHFFFAOYSA-N
    FDA UNII
    I0OU31PUI5
    an analgesic
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    1-acetyloxyethyl 2-(3-fluoro-4-phenylphenyl)propanoate
    2.1.2 InChI
    InChI=1S/C19H19FO4/c1-12(19(22)24-14(3)23-13(2)21)16-9-10-17(18(20)11-16)15-7-5-4-6-8-15/h4-12,14H,1-3H3
    2.1.3 InChI Key
    ALIVXCSEERJYHU-UHFFFAOYSA-N
    2.2 Other Identifiers
    2.2.1 UNII
    I0OU31PUI5
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Fp 83

    2. Fp-83

    3. Fp83

    2.3.2 Depositor-Supplied Synonyms

    1. 91503-79-6

    2. Ropion

    3. Lfp 83

    4. Fp 83

    5. Fp-83

    6. I0ou31pui5

    7. Lfp-83

    8. Dtxsid8048600

    9. Fp83

    10. Dtxcid1028526

    11. (1,1'-biphenyl)-4-acetic Acid, 2-fluoro-alpha-methyl-, 1-(acetyloxy)ethyl Ester

    12. Refchem:141041

    13. 1-(acetyloxy)ethyl 2-(2-fluoro-(1,1'-biphenyl)-4-yl)propanoate

    14. 1-acetoxyethyl 2-(2-fluoro-[1,1'-biphenyl]-4-yl)propanoate

    15. 1-acetyloxyethyl 2-(3-fluoro-4-phenylphenyl)propanoate

    16. 1-acetoxyethyl 2-(2-fluoro-4-biphenylyl)propionate

    17. Mfcd00900049

    18. Lipfen

    19. Lfp 83;ropiopn;lfp-83;lfp83

    20. Flurbiprofen Axetil (jan)

    21. Flurbiprofen Axetil [jan]

    22. Lipo-flurbiprofen Axetil

    23. Liposomal Flurbiprofen Axetil

    24. Cas-91503-79-6

    25. C19h19fo4

    26. Unii-i0ou31pui5

    27. Lfp83

    28. Ncgc00182710-01

    29. Ncgc00182710-02

    30. 2-fluoro-a-methyl-[1,1'-biphenyl]-4-acetic Acid 1-(acetyloxy)ethyl Ester; Flurbiprofen Axetil

    31. 1-acetoxyethyl-2-(2-fluoro-4-biphenylyl)propionate

    32. Ropion (tn)

    33. 4-biphenylacetic Acid, 2-fluoro-alpha-methyl-, 1-acetoxyethyl Ester

    34. 2-fluoro-alpha-methyl-(1,1'-biphenyl)-4-acetic Acid 1-(acetyloxy)ethyl Ester

    35. Orb1304142

    36. Schembl1649401

    37. Chembl3183067

    38. Schembl29370747

    39. Chebi:31627

    40. Hms5085j04

    41. Msk10984

    42. Tox21_113023

    43. Ac-455

    44. Flurbiprofen Axetil [who-dd]

    45. S6457

    46. Akos024464989

    47. Tox21_113023_1

    48. Db14938

    49. Ds-8257

    50. Fa23508

    51. Da-33622

    52. Hy-101481

    53. Cs-0021519

    54. F1176

    55. D01475

    56. F17835

    57. Sbi-0654123.0001

    58. 1-acetoxyethyl-2-(2-fluoro-4-biphenyl)propionate

    59. 1-acetoxyethyl 2-(2-fluoro-4-biphenylyl)propanoate

    60. Q27280207

    61. 1-(acetyloxy)ethyl 2-(2-fluorobiphenyl-4-yl)propanoate

    62. Acetoxyethyl 2-(2-fluoro-[1,1'-biphenyl]-4-yl)propanoate

    63. 1-(acetyloxy)ethyl 2-(2-fluoro[1,1'-biphenyl]-4-yl)propanoate

    64. 2-fluoro-a-methyl-[1,1'-biphenyl]-4-acetic Acid 1-(acetyloxy)ethyl Ester

    65. (1,1'-biphenyl)-4-acetic Acid, 2-fluoro-.alpha.-methyl-, 1-(acetyloxy)ethyl Ester

    66. Lfp 83; Ropiopn; 1-acetoxyethyl 2-(2-fluoro-4-biphenylyl)propionate; 1-acetoxyethyl 2-(2-fluoro-[1,1'-biphenyl]-4-yl)propanoate

    2.4 Create Date
    2005-03-25
    3 Chemical and Physical Properties
    Molecular Weight 330.3 g/mol
    Molecular Formula C19H19FO4
    XLogP34.9
    Hydrogen Bond Donor Count0
    Hydrogen Bond Acceptor Count5
    Rotatable Bond Count7
    Exact Mass Da
    Monoisotopic Mass Da
    Topological Polar Surface Area52.6
    Heavy Atom Count24
    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 Count1
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Anti-Inflammatory Agents, Non-Steroidal

    Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.

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