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    Sulfameter

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    PharmaCompass
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    2D Structure
    Also known as: 651-06-9, 5-methoxysulfadiazine, Sulfamethoxydiazine, Sulfametoxydiazine, Sulfamethoxine, Sulfametin
    Molecular Formula
    C11H12N4O3S
    Molecular Weight
    280.31  g/mol
    InChI Key
    GPTONYMQFTZPKC-UHFFFAOYSA-N
    FDA UNII
    3L179F09D6
    Long acting sulfonamide used in leprosy, urinary, and respiratory tract infections.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    4-amino-N-(5-methoxypyrimidin-2-yl)benzenesulfonamide
    2.1.2 InChI
    InChI=1S/C11H12N4O3S/c1-18-9-6-13-11(14-7-9)15-19(16,17)10-4-2-8(12)3-5-10/h2-7H,12H2,1H3,(H,13,14,15)
    2.1.3 InChI Key
    GPTONYMQFTZPKC-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    COC1=CN=C(N=C1)NS(=O)(=O)C2=CC=C(C=C2)N
    2.2 Other Identifiers
    2.2.1 UNII
    3L179F09D6
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Sulfamethoxydiazine

    2. Sulfamethoxydine

    3. Sulfametin

    4. Sulfametorinum

    5. Sulfametoxidine

    6. Sulfametoxydiazine

    7. Sulphamethoxydiazine

    2.3.2 Depositor-Supplied Synonyms

    1. 651-06-9

    2. 5-methoxysulfadiazine

    3. Sulfamethoxydiazine

    4. Sulfametoxydiazine

    5. Sulfamethoxine

    6. Sulfametin

    7. Sulfamethoxypyrimidine

    8. 4-amino-n-(5-methoxypyrimidin-2-yl)benzenesulfonamide

    9. Sulphamethoxydiazine

    10. Ultrax

    11. Sulla

    12. Sulfametorine

    13. Sulphameter

    14. Methoxypyrimal

    15. Sulfamethoxydin

    16. Berlicid

    17. Sulfa-5-methoxypyrimidine

    18. Sulfamethorine

    19. Longasulf

    20. Supramid

    21. Bayrena

    22. Dairena

    23. Durenat

    24. Juvoxin

    25. Kinecid

    26. Kirocid

    27. Kiron

    28. Ahr-857

    29. Solfametossidiazina

    30. Sulfametoxipirimidine

    31. Sulfameter [usan]

    32. 2-sulfanilamido-5-methoxypyrimidine

    33. 4-amino-n-(5-methoxy-2-pyrimidinyl)benzenesulfonamide

    34. 5-methoxy-2-sulfanilamidopyrimidine

    35. Sulfamethoxydiazin

    36. Sulfametoxidiazina

    37. Bayer 5400

    38. Sulfametoxydiazinum

    39. Benzenesulfonamide, 4-amino-n-(5-methoxy-2-pyrimidinyl)-

    40. 2-(4-aminobenzenesulfonamido)-5-methoxypyrimidine

    41. 2-sulfanilamido-5-methoxypyrimidin

    42. Sulfamethoxidiazine

    43. Sh 613

    44. Nsc 683528

    45. N(sup 1)-(5-methoxy-2-pyrimidinyl)sulfanilamide

    46. Sulfameter (bayrena)

    47. 4-amino-n-(5-methoxypyrimidin-2-yl)benzene-1-sulfonamide

    48. Sulfametoxydiazine [inn]

    49. I-2586

    50. Nsc-683528

    51. Nsc-757874

    52. Chebi:53727

    53. Bay-5400

    54. Sulfameter (usan)

    55. Nsc683528

    56. Sh-613

    57. Sulfanilamide, N(sup 1)-(5-methoxy-2-pyrimidinyl)-

    58. 3l179f09d6

    59. Sulfametoxydiazine;5-methoxysulfadiazine

    60. Ncgc00016530-01

    61. Sulfametinum

    62. Benzenesulfonamide, 4-amino-n-(5-methoxy-2-pyridimidinyl)-

    63. Cas-651-06-9

    64. Sulfametoxydiazine (inn)

    65. Dsstox_cid_3613

    66. N(1)-(5-methoxy-2-pyrimidinyl)sulfanilamide

    67. Dsstox_rid_77110

    68. Dsstox_gsid_23613

    69. Solfametossidiazina [dcit]

    70. Sulfametoxydiazinum [inn-latin]

    71. Sulfametoxidiazina [inn-spanish]

    72. Sr-01000721917

    73. Einecs 211-480-8

    74. Brn 0621130

    75. N1-(5-methoxy-2-pyrimidinyl)sulfanilamide

    76. 2-sulfanilamido-5-methoxypyrimidin [german]

    77. Unii-3l179f09d6

    78. Mfcd00006067

    79. Prestwick_1048

    80. Sulla (tn)

    81. Spectrum_001149

    82. Sulfameter [mi]

    83. Prestwick0_000769

    84. Prestwick1_000769

    85. Prestwick2_000769

    86. Prestwick3_000769

    87. Spectrum2_001428

    88. Spectrum3_001463

    89. Spectrum4_000426

    90. Spectrum5_000981

    91. 2-sulfa-5-methoxypyrimidine

    92. Oprea1_482593

    93. Schembl79417

    94. Bspbio_000818

    95. Bspbio_002985

    96. Kbiogr_000752

    97. Kbioss_001629

    98. 5-25-12-00525 (beilstein Handbook Reference)

    99. Mls000069640

    100. Bidd:gt0693

    101. Divk1c_000468

    102. Spectrum1501155

    103. Spbio_001536

    104. Spbio_002757

    105. Sulfamethoxydiazine / Sulfamete

    106. Bpbio1_000900

    107. Chembl1200359

    108. Dtxsid5023613

    109. Sulfameter [orange Book]

    110. Gptonymqftzpkc-uhfffaoysa-

    111. Hms501h10

    112. Kbio1_000468

    113. Kbio2_001629

    114. Kbio2_004197

    115. Kbio2_006765

    116. Kbio3_002485

    117. Zinc49142

    118. Ninds_000468

    119. Hms1570i20

    120. Hms1921l15

    121. Hms2092j03

    122. Hms2097i20

    123. Hms2233b12

    124. Hms3374j11

    125. Hms3655a11

    126. Hms3714i20

    127. Pharmakon1600-01501155

    128. Sulfametoxydiazine [who-dd]

    129. Amy38159

    130. Hy-b0213

    131. Tox21_110478

    132. Ccg-38965

    133. Nsc757874

    134. S1618

    135. Akos015897255

    136. Sulfameter 100 Microg/ml In Methanol

    137. Tox21_110478_1

    138. Db06821

    139. Idi1_000468

    140. Ncgc00016530-02

    141. Ncgc00016530-03

    142. Ncgc00016530-04

    143. Ncgc00016530-06

    144. Ncgc00016530-07

    145. Ncgc00094915-01

    146. Ncgc00094915-02

    147. Ac-19932

    148. Ac-32614

    149. As-13912

    150. Smr000058215

    151. Sbi-0051665.p002

    152. Db-054761

    153. Ab00052227

    154. Ft-0632748

    155. Sw197118-3

    156. 51s069

    157. D02517

    158. Sulfameter, Vetranal(tm), Analytical Standard

    159. Ab00052227-11

    160. Ab00052227_12

    161. Ab00052227_13

    162. A834976

    163. Sr-01000721917-2

    164. Sr-01000721917-3

    165. W-104807

    166. Brd-k87492696-001-05-8

    167. Brd-k87492696-001-09-0

    168. Q15410181

    169. 4-azanyl-n-(5-methoxypyrimidin-2-yl)benzenesulfonamide

    170. Z1522567176

    171. 4-amino-n-[5-(methyloxy)pyrimidin-2-yl]benzenesulfonamide

    2.4 Create Date
    2005-03-25
    3 Chemical and Physical Properties
    Molecular Weight 280.31 g/mol
    Molecular Formula C11H12N4O3S
    XLogP30.4
    Hydrogen Bond Donor Count2
    Hydrogen Bond Acceptor Count7
    Rotatable Bond Count4
    Exact Mass280.06301143 g/mol
    Monoisotopic Mass280.06301143 g/mol
    Topological Polar Surface Area116 Ų
    Heavy Atom Count19
    Formal Charge0
    Complexity368
    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

    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.)

    Leprostatic Agents

    Substances that suppress Mycobacterium leprae, ameliorate the clinical manifestations of leprosy, and/or reduce the incidence and severity of leprous reactions. (See all compounds classified as Leprostatic Agents.)

    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

    J01E - Sulfonamides and trimethoprim

    J01ED - Long-acting sulfonamides

    J01ED04 - Sulfametoxydiazine