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Chemistry

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Also known as: 80-35-3, Sulphamethoxypyridazine, Midicel, Sulfapyridazine, Depovernil, Sulfalex

Molecular Formula

C₁₁H₁₂N₄O₃S

Molecular Weight

280.31 g/mol

InChI Key

VLYWMPOKSSWJAL-UHFFFAOYSA-N

FDA UNII

T034E4NS2Z

A sulfanilamide antibacterial agent.

1 2D Structure

Sulfamethoxypyridazine

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

4-amino-N-(6-methoxypyridazin-3-yl)benzenesulfonamide

2.1.2 InChI

InChI=1S/C11H12N4O3S/c1-18-11-7-6-10(13-14-11)15-19(16,17)9-4-2-8(12)3-5-9/h2-7H,12H2,1H3,(H,13,15)

2.1.3 InChI Key

VLYWMPOKSSWJAL-UHFFFAOYSA-N

2.1.4 Canonical SMILES

COC1=NN=C(C=C1)NS(=O)(=O)C2=CC=C(C=C2)N

2.2 Other Identifiers

2.2.1 UNII

T034E4NS2Z

2.3 Synonyms

2.3.1 MeSH Synonyms

1. Sulfapyridazine

2. Sulphamethoxypyridazine

2.3.2 Depositor-Supplied Synonyms

1. 80-35-3

2. Sulphamethoxypyridazine

3. Midicel

4. Sulfapyridazine

5. Depovernil

6. Sulfalex

7. Sulfametoxipiridazine

8. Spofadazine

9. Sulfdurazin

10. Lederkyn

11. Longin

12. 3-sulfa-6-methoxypyridazine

13. Sulfamethoxypyridazinum

14. Lisulfen

15. Petrisul

16. Piridolo

17. Quinoseptyl

18. Retasulfin

19. Sulfametoxipiridazina

20. Sulfozona

21. Sultirene

22. Altezol

23. Davosin

24. Lentac

25. Medicel

26. Midikel

27. Myasul

28. Opinsul

29. Paramid

30. Retamid

31. Slosul

32. Vinces

33. Durox

34. Kinex

35. Kynex

36. Smop

37. Solfametossipiridazina

38. Paramid Supra

39. 3-methoxy-6-sulfanylamidopyridazine

40. 3-sulfanilamide-6-methoxypyridazine

41. 3-sulfanilamido-6-methoxypyridazine

42. 6-methoxy-3-sulfanilamidopyridazine

43. 6-sulfanilamido-3-methoxypyridazine

44. 4-amino-n-(6-methoxypyridazin-3-yl)benzenesulfonamide

45. Retasulphine

46. 3-(p-aminobenzenesulfamido)-6-methoxypyridazine

47. 3-p-aminobenzenesulphonamido-6-methoxypyridazine

48. Benzenesulfonamide, 4-amino-n-(6-methoxy-3-pyridazinyl)-

49. Sulfamethoxipyridazine

50. 4-amino-n-(6-methoxy-3-pyridazinyl)benzenesulfonamide

51. 4-amino-n-(6-methoxy-3-pyridazinyl)-benzenesulfonamide

52. Cl 13494

53. 6-methoxy-3-pyridazinylsulfanilamide

54. Sulfamethoxypyridazine [inn]

55. Rp 7522

56. Chebi:102516

57. 3-(4-aminobenzenesulfonamido)-6-methoxypyridazine

58. N(sup 1)-(6-methoxy-3-pyridazinyl)sulfanilamide

59. Nsc-757875

60. Mls000069641

61. T034e4ns2z

62. N(1)-(6-methoxy-3-pyridazinyl)sulfanilamide

63. Ncgc00016324-01

64. Cl-13494

65. N-(6-methoxy-3-pyridazinyl)sulfanilamide

66. Smr000018386

67. Sulfamethoxipyridazinum

68. Dsstox_cid_3611

69. Dsstox_rid_77108

70. Dsstox_gsid_23611

71. Sulfamethoxypyridazine (inn)

72. Sulfamethoxypyridazine 100 Microg/ml In Acetonitrile

73. Cas-80-35-3

74. Solfametossipiridazina [dcit]

75. Sr-01000000179

76. Sulfamethoxypyridazinum [inn-latin]

77. Sulfametoxipiridazina [inn-spanish]

78. Einecs 201-272-5

79. Brn 0277076

80. Unii-t034e4ns2z

81. Kineks

82. N1-(6-methoxy-3-pyridazinyl)sulfanilamide

83. Lederkyn (tn)

84. Prestwick_118

85. 4-amino-n-(6-methoxy-3-pyridazinyl)benzolsulfonamid

86. Sulfamethoxypyridazine [usp:inn:ban]

87. Spectrum_001151

88. Opera_id_698

89. Prestwick0_000724

90. Prestwick1_000724

91. Prestwick2_000724

92. Prestwick3_000724

93. Pyridazine, Sulfamethoxy-

94. Spectrum2_001429

95. Spectrum3_001462

96. Spectrum4_000430

97. Spectrum5_001187

98. Epitope Id:122239

99. Sulphamethazine Sodium Salt

100. Oprea1_275757

101. Schembl93617

102. Bspbio_000648

103. Bspbio_002983

104. Kbiogr_000760

105. Kbioss_001631

106. 5-25-12-00424 (beilstein Handbook Reference)

107. Mls000100719

108. Mls001148433

109. Divk1c_000239

110. Spectrum1501156

111. Spbio_001538

112. Spbio_002587

113. Bpbio1_000714

114. Chembl268869

115. Sulfanilamide, N(sup 1)-(6-methoxy-3-pyridazinyl)-

116. 4-amino-n-(6-methoxy-pyridazin-3-yl)-benzenesulfonamide

117. Benzenesulfonamide,4-amino-n-(6-methoxy-3-pyridazinyl)-

118. Dtxsid5023611

119. Hms500l21

120. Kbio1_000239

121. Kbio2_001631

122. Kbio2_004199

123. Kbio2_006767

124. Kbio3_002483

125. Zinc49141

126. Ninds_000239

127. Hms1570a10

128. Hms1921l17

129. Hms2092j05

130. Hms2097a10

131. Hms2234f17

132. Hms3652h21

133. Hms3714a10

134. Pharmakon1600-01501156

135. Sulfamethoxypyridazine [mi]

136. 3-methoxy-6-sulfanilamidopyridazine

137. Hy-b1387

138. Tox21_110373

139. Ccg-38976

140. Mfcd00057372

141. Nsc757875

142. S4250

143. Sulfamethoxypyridazine [mart.]

144. Akos000605846

145. Tox21_110373_1

146. Cs-4821

147. Db13773

148. Nsc 757875

149. Sdccgmls-0003277.p003

150. Sulfamethoxypyridazine [who-dd]

151. Sulfamethoxypyridazine [who-ip]

152. Idi1_000239

153. Ncgc00016324-02

154. Ncgc00016324-03

155. Ncgc00016324-04

156. Ncgc00016324-05

157. Ncgc00016324-06

158. Ncgc00016324-08

159. Ncgc00016324-09

160. Ncgc00022232-03

161. Ncgc00022232-04

162. Ac-12005

163. Ac-32613

164. Bs-32820

165. Sbi-0051666.p002

166. Sulfamethoxypyridazine, Analytical Standard

167. Ab00052228

168. Ft-0653623

169. S0591

170. Sw196429-3

171. Sulfamethoxypyridazinum [who-ip Latin]

172. D02439

173. D70409

174. Sulfanilamide, N1-(6-methoxy-3-pyridazinyl)-

175. Ab00052228_12

176. Sulfamethoxypyridazine 100 Microg/ml In Methanol

177. A839894

178. Sulfamethoxypyridazine 1000 Microg/ml In Methanol

179. Q7636177

180. Sr-01000000179-3

181. Sr-01000000179-4

182. W-104237

183. Brd-k00938507-001-05-3

184. Brd-k00938507-001-13-7

185. 4-amino-n-[6-(methyloxy)pyridazin-3-yl]benzenesulfonamide

186. Sulfamethoxypyridazine, Vetranal(tm), Analytical Standard

187. Sulfamethoxypyridazine, European Pharmacopoeia (ep) Reference Standard

2.4 Create Date

2005-03-25

3 Chemical and Physical Properties

Molecular Formula	C₁₁H₁₂N₄O₃S
Molecular Weight	280.31 g/mol
XLogP3	0.3
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	7
Rotatable Bond Count	4
Exact Mass	280.06301143 g/mol
Monoisotopic Mass	280.06301143 g/mol
Topological Polar Surface Area	116 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	376
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-Bacterial Agents

Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)

4.2 ATC Code

J - Antiinfectives for systemic use

J01 - Antibacterials for systemic use

J01E - Sulfonamides and trimethoprim

J01ED - Long-acting sulfonamides

J01ED05 - Sulfamethoxypyridazine

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