Sulfisomidine

Sulfisomidine
Clinical data
Routes of; administration	Oral
ATC code	J01EB01 (WHO) ;
Pharmacokinetic data
Metabolism	Minor acetylation
Excretion	Renal, 85%
Identifiers
	IUPAC name 4-amino-N-(2,6-dimethylpyrimidin-4-yl); benzenesulfonamide;
CAS Number	515-64-0 ;
PubChem CID	5343;
ChemSpider	5150 ;
UNII	W03L3ODK6E;
KEGG	D01526 ;
ChEBI	CHEBI:32166 ;
ChEMBL	ChEMBL485696 ;
CompTox Dashboard (EPA)	DTXSID1046390 ;
ECHA InfoCard	100.007.460
Chemical and physical data
Formula	C12H14N4O2S
Molar mass	278.33 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES O=S(=O)(Nc1nc(nc(c1)C)C)c2ccc(N)cc2;
	InChI InChI=1S/C12H14N4O2S/c1-8-7-12(15-9(2)14-8)16-19(17,18)11-5-3-10(13)4-6-11/h3-7H,13H2,1-2H3,(H,14,15,16) ; Key:YZMCKZRAOLZXAZ-UHFFFAOYSA-N ;
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Sulfisomidine (INN), also known as sulphasomidine (BAN until 2003),[1] sulfamethin and sulfaisodimidine, is a sulfonamide antibacterial. It is closely related to sulfadimidine.

References

"Changing substance names from BANs to rINNs" (PDF). Archived from the original on 2005-08-27.CS1 maint: bot: original URL status unknown (link) (34.5 KiB). United Kingdom Medicines and Healthcare products Regulatory Agency (December 12, 2003). Retrieved on 2007-08-26 through Archive.org.

External links

Melander A, Bitzén PO, Olsson S (1982). "Therapeutic equivalence of sulfaisodimidine 2 g twice daily and 1 g four times daily in lower urinary tract infections". Acta Medica Scandinavica. 211 (5): 361–4. doi:10.1111/j.0954-6820.1982.tb01962.x. PMID 7051761.

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[1] "Changing substance names from BANs to rINNs" (PDF). Archived from the original on 2005-08-27.CS1 maint: bot: original URL status unknown (link) (34.5 KiB). United Kingdom Medicines and Healthcare products Regulatory Agency (December 12, 2003). Retrieved on 2007-08-26 through Archive.org.