Prestwick3_000715

Synopsis, Chemistry

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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

Prestwick3_000715

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 Formula	C₁₀H₉ClN₄O₂S
Molecular Weight	284.72 g/mol
XLogP3	1
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	3
Exact Mass	284.0134744 g/mol
Monoisotopic Mass	284.0134744 g/mol
Topological Polar Surface Area	106 Å²
Heavy Atom Count	18
Formal Charge	0
Complexity	365
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	1

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.)