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Sulfametoxydiazine

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Chemical compound
Pharmaceutical compound
Sulfametoxydiazine
Clinical data
ATC code
Identifiers
  • 4-amino-N-(5-methoxy-2-pyrimidinyl)benzenesulfonamide
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
NIAID ChemDB
CompTox Dashboard(EPA)
ECHA InfoCard100.010.438Edit this at Wikidata
Chemical and physical data
FormulaC11H12N4O3S
Molar mass280.30 g·mol−1
3D model (JSmol)
  • O=S(=O)(Nc1ncc(OC)cn1)c2ccc(N)cc2
  • 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) checkY
  • Key:GPTONYMQFTZPKC-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Sulfametoxydiazine (INN) orsulfamethoxydiazine (USAN:sulfameter) is a long-actingsulfonamideantibacterial.[1] It is used as aleprostatic agent and in the treatment ofurinary tract infections.[2]

Sulfamethoxydiazine is also used to treat and prevent diseases in animals. Because of its relatively long persistence, sulfamethoxydiazine residue can be detected in meat, dairy, and eggs, and is considered hazardous to human health. The United States and Japan both prohibit sulfamethoxydiazine residue in food, whereas theCodex Alimentarius Commission states that the maximum limit for sulfonamides in animal tissues is 100 μg/kg.[1]

References

[edit]
  1. ^abWu Y, Yu S, Yu F, Yan N, Qu L, Zhang H (October 2011). "Chemiluminescence enzyme immunoassay for the determination of sulfamethoxydiazine".Spectrochimica Acta Part A.81 (1):544–547.Bibcode:2011AcSpA..81..544W.doi:10.1016/j.saa.2011.06.047.PMID 21795101.
  2. ^Burros HM, Gillenwater JY (July 1965). "Clinical Experience with Sulfamethoxydiazine* in Urinary Tract Infections".The Journal of Urology.94 (1):86–88.doi:10.1016/S0022-5347(17)63576-6.PMID 14319481.
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