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    Technical details about Carbaspirin Calcium, learn more about the structure, uses, toxicity, action, side effects and more

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    Carbaspirin Calcium

    APIs // Active Pharmaceutical Ingredients

    DOSSIERs // Finished Dosage Forms

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

    PharmaCompass

    Inke S.A: APIs manufacturing plant.

    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

    2D Structure
    1. Also known as: 5749-67-7, Carbaspirin calcium, Alcacyl, Rheomin, Solupsan, Iromin
    Molecular Formula
    C19H18CaN2O9
    Molecular Weight
    458.4  g/mol
    InChI Key
    VYMUGTALCSPLDM-UHFFFAOYSA-L
    FDA UNII
    N667F17JP1
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    calcium;2-acetyloxybenzoate;urea
    2.1.2 InChI
    InChI=1S/2C9H8O4.CH4N2O.Ca/c2*1-6(10)13-8-5-3-2-4-7(8)9(11)12;2-1(3)4;/h2*2-5H,1H3,(H,11,12);(H4,2,3,4);/q;;;+2/p-2
    2.1.3 InChI Key
    VYMUGTALCSPLDM-UHFFFAOYSA-L
    2.1.4 Canonical SMILES
    CC(=O)OC1=CC=CC=C1C(=O)[O-].CC(=O)OC1=CC=CC=C1C(=O)[O-].C(=O)(N)N.[Ca+2]
    2.2 Other Identifiers
    2.2.1 UNII
    N667F17JP1
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Calcium Acetylsalicylate Complex With Urea

    2. Calcium Acetylsalicylic Carbamidate

    3. Calcium Carbasalate

    4. Calurin

    5. Carbaspirin Calcium

    6. Carbosalate Calcium

    2.3.2 Depositor-Supplied Synonyms

    1. 5749-67-7

    2. Carbaspirin Calcium

    3. Alcacyl

    4. Rheomin

    5. Solupsan

    6. Iromin

    7. Omegin

    8. Calcium Carbaspirin

    9. Carbaspirin Calcium [usan]

    10. Calcium Acetylsalicylate Complex With Urea

    11. Carbasalate Calcium [inn]

    12. N667f17jp1

    13. Benzoic Acid, 2-(acetyloxy)-, Calcium Salt, Compd. With Urea (1:1)

    14. Salicylic Acid Acetate Calcium Salt, Compound With Urea (1:1) Complex

    15. Carbasalate Calcium (inn)

    16. Carbaspirin Calcium (usan)

    17. Carbasalate Calcique

    18. Calpirinsan

    19. Carbasalatcalcium

    20. Carbaspirin Calium

    21. Calcium;2-acetyloxybenzoate;urea

    22. Carbasalato Calcico

    23. Carbasalatum Calcicum

    24. Unii-n667f17jp1

    25. Carbasalate Calcique [inn-french]

    26. Carbasalato Calcico [inn-spanish]

    27. Carbasalatum Calcicum [inn-latin]

    28. Carbasalate?calcium

    29. Calcium; 2-acetyloxybenzoate; Urea

    30. Einecs 227-273-0

    31. Chembl3833325

    32. Dtxsid90206099

    33. Alcacyl; Rheomin; Solupsan; Omegin

    34. Bcp12255

    35. Carbasalate Calcium [mart.]

    36. Carbasalate Calcium [who-dd]

    37. Akos015895683

    38. Akos025401461

    39. Db13612

    40. Calcium Acetylsalicylate Carbamide

    41. Ac-18297

    42. As-13259

    43. Carbasalate Calcium [ep Monograph]

    44. D03385

    45. A831468

    46. Q2203957

    47. Calcium Acetylsalicylate Complex With Urea [mi]

    2.4 Create Date
    2005-08-08
    3 Chemical and Physical Properties
    Molecular Weight 458.4 g/mol
    Molecular Formula C19H18CaN2O9
    Hydrogen Bond Donor Count2
    Hydrogen Bond Acceptor Count9
    Rotatable Bond Count4
    Exact Mass458.0638210 g/mol
    Monoisotopic Mass458.0638210 g/mol
    Topological Polar Surface Area202 Ų
    Heavy Atom Count31
    Formal Charge0
    Complexity235
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count4
    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. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)

    4.2 ATC Code

    B - Blood and blood forming organs

    B01 - Antithrombotic agents

    B01A - Antithrombotic agents

    B01AC - Platelet aggregation inhibitors excl. heparin

    B01AC08 - Carbasalate calcium

    N - Nervous system

    N02 - Analgesics

    N02B - Other analgesics and antipyretics

    N02BA - Salicylic acid and derivatives

    N02BA15 - Carbasalate calcium

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