Sulfamethizole
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Clinical data | |
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AHFS/Drugs.com | Micromedex Detailed Consumer Information |
MedlinePlus | a682231 |
ATC code | |
Pharmacokinetic data | |
Protein binding | 98–99% |
Elimination half-life | 3–8 hours |
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CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.005.129 ![]() |
Chemical and physical data | |
Formula | C9H10N4O2S2 |
Molar mass | 270.33 g·mol−1 |
3D model (JSmol) | |
Melting point | 208 °C (406 °F) |
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Sulfamethizole is a sulfonamide antibiotic.[1]
References[]
- ^ Ayankojo, Akinrinade George; Tretjakov, Aleksei; Reut, Jekaterina; Boroznjak, Roman; Öpik, Andres; Rappich, Jörg; Furchner, Andreas; Hinrichs, Karsten; Syritski, Vitali (2016). "Molecularly Imprinted Polymer Integrated with a Surface Acoustic Wave Technique for Detection of Sulfamethizole". Anal. Chem. 88 (2): 1476–1484. doi:10.1021/acs.analchem.5b04735. PMID 26704414.
- 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.
- 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.
- 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.
Categories:
- Sulfonamide antibiotics
- Thiadiazoles
- Antibiotic stubs
- Blood and blood forming organ drug stubs
- Dermatologic drug stubs