loader
Please Wait
Applying Filters...

Bora CDMO Bora CDMO

X
menu

    Market Place

    Market Place

    Post Enquiry

    Post Enquiry
    menu

    Technical details about Prestwick3_000715, learn more about the structure, uses, toxicity, action, side effects and more

    Client Email Product
    Menu

    Prestwick3_000715

    APIs // Active Pharmaceutical Ingredients

    ANALYTICAL SOLUTION(s)

    PharmaCompass

    Phyton is a World Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.

    Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.

    2D Structure
    1. Also known as: Sulfachloropyridazine, 80-32-0, 4-amino-n-(6-chloropyridazin-3-yl)benzenesulfonamide, Sulphachlorpyridazine, Nefrosul, Sonilyn
    Molecular Formula
    C10H9ClN4O2S
    Molecular Weight
    284.72  g/mol
    InChI Key
    XOXHILFPRYWFOD-UHFFFAOYSA-N
    FDA UNII
    P78D9P90C0
    A sulfonamide antimicrobial used for urinary tract infections and in veterinary medicine.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    4-amino-N-(6-chloropyridazin-3-yl)benzenesulfonamide
    2.1.2 InChI
    InChI=1S/C10H9ClN4O2S/c11-9-5-6-10(14-13-9)15-18(16,17)8-3-1-7(12)2-4-8/h1-6H,12H2,(H,14,15)
    2.1.3 InChI Key
    XOXHILFPRYWFOD-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    C1=CC(=CC=C1N)S(=O)(=O)NC2=NN=C(C=C2)Cl
    2.2 Other Identifiers
    2.2.1 UNII
    P78D9P90C0
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Monosodium Salt Sulfachlorpyridazine

    2. Sulfachloropyridazine

    3. Sulfachlorpyridazine, Monosodium Salt

    4. Sulphachlorpyridazine

    2.3.2 Depositor-Supplied Synonyms

    1. Sulfachloropyridazine

    2. 80-32-0

    3. 4-amino-n-(6-chloropyridazin-3-yl)benzenesulfonamide

    4. Sulphachlorpyridazine

    5. Nefrosul

    6. Sonilyn

    7. N1-(6-chloro-3-pyridazinyl)sulfanilamide

    8. 4-amino-n-(6-chloro-3-pyridazinyl)benzenesulfonamide

    9. Sulfacloropiridazina

    10. Durasulf

    11. Sulfachlorpyridazinum

    12. Vetisulid

    13. Benzenesulfonamide, 4-amino-n-(6-chloro-3-pyridazinyl)-

    14. Ba 10370

    15. Sulfachloropyridizine

    16. Chebi:59057

    17. Nsc-757858

    18. Mls000777734

    19. N(sup 1)-(6-chloro-3-pyridazinyl)sulfanilamide

    20. P78d9p90c0

    21. 4-amino-n-(6-chloropyridazin-3-yl)-benzenesulfonamide

    22. Cas-80-32-0

    23. Ncgc00016323-01

    24. Ncgc00016323-04

    25. Cluricol

    26. Smr000414174

    27. N(1)-(6-chloro-3-pyridazinyl)sulfanilamide

    28. Dsstox_cid_25265

    29. Dsstox_rid_80778

    30. Dsstox_gsid_45265

    31. Sulfachloropyridazine 100 Microg/ml In Acetonitrile

    32. 4-amino-n-(6-chloro-pyridazin-3-yl)-benzenesulfonamide

    33. Vetisulid (veterinary)

    34. Prinzone Vet.

    35. Solfaclorpiridazina

    36. Solfaclorpiridazina [dcit]

    37. Scp

    38. Sulphachloropyridazine

    39. Sulfachlorpyridazinum [inn-latin]

    40. Sr-01000773478

    41. Sulfacloropiridazina [inn-spanish]

    42. Einecs 201-269-9

    43. N1-(6-chlor-3-pyridazinyl)sulfanilamid

    44. Cosulid

    45. Unii-p78d9p90c0

    46. Nefrosul (tn)

    47. Prestwick_130

    48. Sulfachlorpyridazine [usp:inn:ban]

    49. Mfcd00057371

    50. Cosumix (salt/mix)

    51. 4-amino-n-(6-chloropyridazin-3-yl)benzene-1-sulfonamide

    52. Spectrum_000127

    53. Prestwick0_000715

    54. Prestwick1_000715

    55. Prestwick2_000715

    56. Prestwick3_000715

    57. Spectrum2_001942

    58. Spectrum3_001221

    59. Spectrum4_000444

    60. Spectrum5_001011

    61. Epitope Id:122243

    62. Cid_6634

    63. Ciba 10370

    64. Oprea1_485631

    65. Schembl94138

    66. Bspbio_000929

    67. Bspbio_002662

    68. Kbiogr_000828

    69. Kbioss_000587

    70. Spectrum1501142

    71. Spbio_002003

    72. Spbio_002850

    73. Bpbio1_001023

    74. Sulfachlorpyridazine (usp/inn)

    75. [(4-aminophenyl)sulfonyl](6-chloropyridazin-3-yl)amine

    76. Chembl1443577

    77. Dtxsid9045265

    78. Bdbm90673

    79. Kbio2_000587

    80. Kbio2_003155

    81. Kbio2_005723

    82. Kbio3_002162

    83. Sulfachlorpyridazine [mi]

    84. Zinc49140

    85. Sulfachlorpyridazine [inn]

    86. Hms1570o11

    87. Hms1921j11

    88. Hms2092f19

    89. Hms2097o11

    90. Hms2766b06

    91. Hms3714o11

    92. Pharmakon1600-01501142

    93. Albb-011657

    94. Hy-b1781

    95. Str03778

    96. Sulfachlorpyridazine [mart.]

    97. Tox21_110372

    98. Tox21_112957

    99. Bbl037369

    100. Ccg-39459

    101. Nsc757858

    102. S3708

    103. Stk315422

    104. Sulfachlorpyridazine [usp-rs]

    105. Sulfachlorpyridazine [who-dd]

    106. Akos000308728

    107. Tox21_110372_1

    108. Cs-7970

    109. Db11461

    110. Nsc 757858

    111. Ncgc00016323-02

    112. Ncgc00016323-03

    113. Ncgc00016323-09

    114. Ncgc00094909-01

    115. Ncgc00094909-02

    116. Sulfachlorpyridazine [green Book]

    117. Ac-12002

    118. N'-(6-chloro-3-pyridazinyl)sulfanilamide

    119. Sbi-0051655.p002

    120. Sulfachlorpyridazine [usp Monograph]

    121. Ab00052217

    122. Ft-0674699

    123. C76571

    124. D05948

    125. Ab00052217_11

    126. Sulfachloropyridazine 100 Microg/ml In Methanol

    127. A839891

    128. Sulfachloropyridazine 1000 Microg/ml In Methanol

    129. Sr-01000773478-2

    130. Sr-01000773478-3

    131. W-104238

    132. 4-amino-n-(6-chloro-3-pyridazinyl)-benzenesulfnamide

    133. Brd-k32021043-001-05-1

    134. Q27126423

    135. 4-amino-n-(6-chloro-3-pyridazinyl)benzenesulfonamide #

    136. 4-azanyl-n-(6-chloranylpyridazin-3-yl)benzenesulfonamide

    137. Pyridazin-3-amine, N-(4-aminophenylsulfonyl)-6-chloro-

    138. Sulfachloropyridazine, Vetranal(tm), Analytical Standard

    139. Sulfachlorpyridazine, United States Pharmacopeia (usp) Reference Standard

    140. N'-[(5z)-7,7-dimethyl-3-oxo-2,6,7,8-tetrahydrocinnolin-5(3h)-ylidene]-n,n-dimethylhydrazonoformamide

    2.4 Create Date
    2005-03-27
    3 Chemical and Physical Properties
    Molecular Weight 284.72 g/mol
    Molecular Formula C10H9ClN4O2S
    XLogP31
    Hydrogen Bond Donor Count2
    Hydrogen Bond Acceptor Count6
    Rotatable Bond Count3
    Exact Mass284.0134744 g/mol
    Monoisotopic Mass284.0134744 g/mol
    Topological Polar Surface Area106 Ų
    Heavy Atom Count18
    Formal Charge0
    Complexity365
    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, 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.)

    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.)

    Post Enquiry
    POST ENQUIRY