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    Furazidin

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

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    2D Structure
    Also known as: Furazidin, 1672-88-4, Furazidine, Akritoin, Furaginum, 1-((3-(5-nitro-2-furyl)allylidene)amino)hydantoin
    Molecular Formula
    C10H8N4O5
    Molecular Weight
    264.19  g/mol
    InChI Key
    DECBQELQORZLLP-UAIOPKHMSA-N
    FDA UNII
    K2R4N34Y9I
    Nitrofuran derivative anti-infective agent used for urinary tract infections.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    1-[(E)-[(E)-3-(5-nitrofuran-2-yl)prop-2-enylidene]amino]imidazolidine-2,4-dione
    2.1.2 InChI
    InChI=1S/C10H8N4O5/c15-8-6-13(10(16)12-8)11-5-1-2-7-3-4-9(19-7)14(17)18/h1-5H,6H2,(H,12,15,16)/b2-1+,11-5+
    2.1.3 InChI Key
    DECBQELQORZLLP-UAIOPKHMSA-N
    2.1.4 Canonical SMILES
    C1C(=O)NC(=O)N1N=CC=CC2=CC=C(O2)[N+](=O)[O-]
    2.1.5 Isomeric SMILES
    C1C(=O)NC(=O)N1/N=C/C=C/C2=CC=C(O2)[N+](=O)[O-]
    2.2 Other Identifiers
    2.2.1 UNII
    K2R4N34Y9I
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Furazidin

    2. Solafur

    2.3.2 Depositor-Supplied Synonyms

    1. Furazidin

    2. 1672-88-4

    3. Furazidine

    4. Akritoin

    5. Furaginum

    6. 1-((3-(5-nitro-2-furyl)allylidene)amino)hydantoin

    7. 1-[(e)-[(e)-3-(5-nitrofuran-2-yl)prop-2-enylidene]amino]imidazolidine-2,4-dione

    8. K2r4n34y9i

    9. Nf 416

    10. F-35

    11. 1-((3-(5-nitro-2-furyl)allylidene)amino)-hydantoin

    12. 1-[(e)-[(z)-3-(5-nitrofuran-2-yl)prop-2-enylidene]amino]imidazolidine-2,4-dione

    13. Furamag

    14. 1-((3-(5-nitrofuran-2-yl)allylidene)-amino)imidazolidine-2,4-dione

    15. 1-(((1e,2e)-3-(5-nitrofuran-2-yl)allylidene)amino)imidazolidine-2,4-dione

    16. 1-{[(1e,2e)-3-(5-nitrofuran-2-yl)prop-2-en-1-ylidene]amino}imidazolidine-2,4-dione

    17. Ccris 1199

    18. 1-(3-(5-nitro-2-furyl)-n-2-propenylidine)amino-hydantoin

    19. Brn 0307076

    20. Unii-k2r4n34y9i

    21. Furagin (tn)

    22. Furazidin [mart.]

    23. Furazidin [who-dd]

    24. 1-[3-(5-nitro-2-furyl)allylidenamino]hydantoin

    25. 4-24-00-01048 (beilstein Handbook Reference)

    26. Schembl3194895

    27. Chembl3707254

    28. Hydantoin, 1-((3-(5-nitro-2-furyl)allylidene)amino)-

    29. Schembl17292896

    30. J01xe03

    31. Dtxsid101030908

    32. Ex-a1974

    33. Bdbm50549808

    34. S3709

    35. Stk368597

    36. Zinc31430194

    37. 1-((3-(5-nitro-2-furanyl)-2-propenylidene)amino)-4-imidazolidinedione

    38. 2,4-imidazolidinedione, 1-((3-(5-nitro-2-furanyl)-2-propenylidene)amino)-

    39. Akos005444359

    40. Ccg-267084

    41. Cs-0798

    42. Db13475

    43. Bs-49182

    44. Hy-77036

    45. D07998

    46. 672f884

    47. A810846

    48. 1-(3-(5-nitro-2-furyl)-n-2-propenylidine)aminohydantoin

    49. 1-(((e)-3-(5-nitrofuran-2-yl)prop-2-enylidene)amino)imidazolidine-2,4-dione

    50. 2,4-imidazolidinedione, 1-[[3-(5-nitro-2-furanyl)-2-propen-1-ylidene]amino]-

    2.4 Create Date
    2006-07-03
    3 Chemical and Physical Properties
    Molecular Weight 264.19 g/mol
    Molecular Formula C10H8N4O5
    XLogP30.5
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count6
    Rotatable Bond Count3
    Exact Mass264.04946937 g/mol
    Monoisotopic Mass264.04946937 g/mol
    Topological Polar Surface Area121 Ų
    Heavy Atom Count19
    Formal Charge0
    Complexity455
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count2
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Anti-Infective Agents, Urinary

    Substances capable of killing agents causing urinary tract infections or of preventing them from spreading. (See all compounds classified as Anti-Infective Agents, Urinary.)

    4.2 ATC Code

    J - Antiinfectives for systemic use

    J01 - Antibacterials for systemic use

    J01X - Other antibacterials

    J01XE - Nitrofuran derivatives

    J01XE03 - Furazidin