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    Sulfisoxazole Diolamine

    FINISHED DOSAGE FORMULATIONS

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    2D Structure
    Also known as: 4299-60-9, Sulfafurazole diolamine, Sulfafurazol 2,2'-imidodiethanol, Sulfisoxazole diolamine [usan], Sulphafurazole diolamine, Sulfisoxazole diolamine [usan:usp]
    Molecular Formula
    C15H24N4O5S
    Molecular Weight
    372.4  g/mol
    InChI Key
    FEPTXVIRMZIGFY-UHFFFAOYSA-N
    FDA UNII
    30S4B46J8B
    A short-acting sulfonamide antibacterial with activity against a wide range of gram- negative and gram-positive organisms.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    4-amino-N-(3,4-dimethyl-1,2-oxazol-5-yl)benzenesulfonamide;2-(2-hydroxyethylamino)ethanol
    2.1.2 InChI
    InChI=1S/C11H13N3O3S.C4H11NO2/c1-7-8(2)13-17-11(7)14-18(15,16)10-5-3-9(12)4-6-10;6-3-1-5-2-4-7/h3-6,14H,12H2,1-2H3;5-7H,1-4H2
    2.1.3 InChI Key
    FEPTXVIRMZIGFY-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CC1=C(ON=C1C)NS(=O)(=O)C2=CC=C(C=C2)N.C(CO)NCCO
    2.2 Other Identifiers
    2.2.1 UNII
    30S4B46J8B
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Ammonium Salt Sulfisoxazole

    2. Diolamine, Sulfisoxazole

    3. Gantrisin

    4. Gantrisin Pediatric

    5. Monolithium Salt Sulfisoxazole

    6. Monosodium Salt Sulfisoxazole

    7. Neoxazoi

    8. Pediatric, Gantrisin

    9. Sulfadimethyloxazole

    10. Sulfafurazol Fna

    11. Sulfafurazole

    12. Sulfasoxizole

    13. Sulfisoxazole

    14. Sulfisoxazole, Ammonium Salt

    15. Sulfisoxazole, Monolithium Salt

    16. Sulfisoxazole, Monosodium Salt

    17. Sulfisoxazole, Monosodium, Monomesylate Salt

    18. Sulfisoxazole, Triammonium Salt

    19. Tl Azole

    20. Tl-azole

    21. Triammonium Salt Sulfisoxazole

    22. V Sul

    23. V-sul

    2.3.2 Depositor-Supplied Synonyms

    1. 4299-60-9

    2. Sulfafurazole Diolamine

    3. Sulfafurazol 2,2'-imidodiethanol

    4. Sulfisoxazole Diolamine [usan]

    5. Sulphafurazole Diolamine

    6. Sulfisoxazole Diolamine [usan:usp]

    7. Nu-445

    8. Sulfafurazole Diethanolamine

    9. Sulfisoxazole (diethanolamine)

    10. 30s4b46j8b

    11. Gantrisin (tn)

    12. N(sup 1)-(3,4-dimethyl-5-isoxazolyl)sulfanilamide Compound With 2,2'-iminodiethanol (1:1)

    13. Benzenesulfonamide, 4-amino-n-(3,4-dimethyl-5-isoxazolyl)-, Compd. With 2,2'-iminobis(ethanol) (1:1)

    14. Sulfisoxazole Diolamine (usan)

    15. 4-amino-n-(3,4-dimethyl-1,2-oxazol-5-yl)benzenesulfonamide;2-(2-hydroxyethylamino)ethanol

    16. Einecs 224-308-1

    17. Unii-30s4b46j8b

    18. Sulfisoxazoldiolamin

    19. Sulfisoxazole Diethanolamine

    20. N-(3,4-dimethylisoxazol-5-yl)sulphanilamide, Compound With 2,2'-iminodiethanol (1:1)

    21. Schembl23466

    22. Chembl1200321

    23. Chebi:88263

    24. Hy-b0323a

    25. Dtxsid90195616

    26. Sulfafurazole Diolamine [mart.]

    27. Sulfisoxazole Diolamine [vandf]

    28. Sulfisoxazole Diethanolamine Salt

    29. Cs-0030851

    30. Sulfafurazole Diethanolamine [who-dd]

    31. Sulfisoxazole Diolamine [orange Book]

    32. Sulfisoxazole Diethanolamine Salt [mi]

    33. D05957

    34. Q27160153

    35. 4-amino-n-(3,4-dimethyl-1,2-oxazol-5-yl)benzene-1-sulfonamide--2,2'-azanediyldi(ethan-1-ol) (1/1)

    2.4 Create Date
    2005-08-08
    3 Chemical and Physical Properties
    Molecular Weight 372.4 g/mol
    Molecular Formula C15H24N4O5S
    Hydrogen Bond Donor Count5
    Hydrogen Bond Acceptor Count9
    Rotatable Bond Count7
    Exact Mass372.14674105 g/mol
    Monoisotopic Mass372.14674105 g/mol
    Topological Polar Surface Area159 Ų
    Heavy Atom Count25
    Formal Charge0
    Complexity402
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count2
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Anti-Infective Agents

    Substances that prevent infectious agents or organisms from spreading or kill infectious agents in order to prevent the spread of infection. (See all compounds classified as Anti-Infective Agents.)