Sulfamethizole

Sulfamethizole

Clinical data
AHFS/Drugs.com	Micromedex Detailed Consumer Information
MedlinePlus	a682231
ATC code	B05CA04 (WHO) D06BA04 (WHO) J01EB02 (WHO) S01AB01 (WHO) QJ01EQ02 (WHO)
Pharmacokinetic data
Protein binding	98–99%
Elimination half-life	3–8 hours
Identifiers
IUPAC name 4-amino-N-(5-methyl-1,3,4-thiadiazol-2-yl)- benzenesulfonamide
CAS Number	144-82-1 Y
PubChem CID	5328
DrugBank	DB00576 Y
ChemSpider	5137 Y
UNII	25W8454H16
KEGG	D00870 Y
ChEBI	CHEBI:9331 Y
ChEMBL	ChEMBL1191 Y
CompTox Dashboard (EPA)	DTXSID5023615
ECHA InfoCard	100.005.129
Chemical and physical data
Formula	C9H10N4O2S2
Molar mass	270.333 g/mol g·mol−1
3D model (JSmol)	Interactive image
SMILES O=S(=O)(Nc1nnc(s1)C)c2ccc(N)cc2
InChI InChI=1S/C9H10N4O2S2/c1-6-11-12-9(16-6)13-17(14,15)8-4-2-7(10)3-5-8/h2-5H,10H2,1H3,(H,12,13) Y Key:VACCAVUAMIDAGB-UHFFFAOYSA-N Y
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Sulfamethizole is a sulfonamide antibiotic.

References

• Ratanajamit C, Skriver M, Nørgaard M, Jepsen P, Schønheyder H, Sørensen H (2003). "Adverse pregnancy outcome in users of sulfamethizole during pregnancy: a population-based observational study". J Antimicrob Chemother. 52 (5): 837–41. doi:10.1093/jac/dkg438. PMID 14519675.{{cite journal}}: CS1 maint: multiple names: authors list (link)
• Kerrn M, Frimodt-Møller N, Espersen F (2003). "Effects of Sulfamethizole and Amdinocillin against Escherichia coli Strains (with Various Susceptibilities) in an Ascending Urinary Tract Infection Mouse Model". Antimicrob Agents Chemother. 47 (3): 1002–9. doi:10.1128/AAC.47.3.1002-1009.2003. PMC 149286. PMID 12604534.{{cite journal}}: CS1 maint: multiple names: authors list (link)
• Watanabe H, Hastings J (1990). "Inhibition of bioluminescence in Photobacterium phosphoreum by sulfamethizole and its stimulation by thymine". Biochim Biophys Acta. 1017 (3): 229–34. doi:10.1016/0005-2728(90)90189-B. PMID 2372557.