Sulfadoxine

Sulfadoxine
Systematic (IUPAC) name
4-Amino-N-(5,6-dimethoxy-4-pyrimidinyl)benzenesulfonamide
Clinical data
AHFS/Drugs.com International Drug Names
Identifiers
CAS Number 2447-57-6 YesY
ATCvet code QJ01EQ13
PubChem CID 17134
DrugBank DB01299 N
ChemSpider 16218 N
UNII 88463U4SM5 N
KEGG D00580 YesY
ChEMBL CHEMBL1539 N
NIAID ChemDB 007816
Chemical data
Formula C12H14N4O4S
Molar mass 310.33 g/mol
 NYesY (what is this?)  (verify)

Sulfadoxine (also spelled sulphadoxine) is an ultra-long-lasting sulfonamide previously used in combination with pyrimethamine to treat or prevent malaria.[1] Due to high levels of resistance, its use is no longer recommended routinely.[2] It is also used, usually in combination with other drugs, to treat or prevent various infections in livestock.[3]

It is on the World Health Organization's List of Essential Medicines, a list of the most important medication needed in a basic health system.[4]

Mechanism of action

Sulfadoxine competitively inhibits dihydropteroate synthase, interfering with folate synthesis.

Synthesis

Sulfadoxine synthesis: U.S. Patent 3,132,139 BE 618639  [5][6]

See also

References

  1. Medical Treatment - Sulphadoxine and Pyrimethamine.
  2. Matondo SI, Temba GS, Kavishe AA, et al. (2014). "High levels of sulphadoxine-pyrimethamine resistance Pfdhfr-Pfdhps quintuple mutations: a cross sectional survey of six regions in Tanzania.". Malar J 13: 152. doi:10.1186/1475-2875-13-152. PMC 3998221. PMID 24751352.
  3. http://en.scientificcommons.org/19483411.
  4. "WHO Model List of EssentialMedicines" (PDF). World Health Organization. October 2013. Retrieved 22 April 2014.
  5. Bretschneider, H.; Richter, W.; Kl�Tzer, W. (1965). "Synthesen des 4-Sulfanilamido-5,6-dimethoxypyrimidins". Monatshefte f�r Chemie 96 (6): 1661. doi:10.1007/BF01185885. replacement character in |last3= at position 3 (help); replacement character in |journal= at position 14 (help)
  6. Gr�Ssner, A.; Montavon, M.; Schnider, O. (1965). "Disubstituierte 4-Sulfanilamido-pyrimidine". Monatshefte f�r Chemie 96 (6): 1677. doi:10.1007/BF01185886. replacement character in |journal= at position 14 (help); replacement character in |last1= at position 3 (help)


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