Sulfisomidine: Difference between revisions

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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 ;
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C12H14N4O2S
Molar mass	278.331 g/mol
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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VisualWikitext

Latest revision as of 13:06, 15 April 2015

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Sulfisomidine (INN), also known as sulphasomidine (BAN until 2003),^[1] sulfamethin and sulfaisodimidine, is a sulfonamide antibacterial. It is closely related to sulfadimidine.

References

↑ Template:PDFlink. 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.

Template:Sulfonamides and trimethoprim

[1] Template:PDFlink. United Kingdom Medicines and Healthcare products Regulatory Agency (December 12, 2003). Retrieved on 2007-08-26 through Archive.org.

[1]

@@ Line 3: / Line 3: @@
 | verifiedrevid = 470473700
 | IUPAC_name = 4-amino-''N''-(2,6-dimethylpyrimidin-4-yl)<br>benzenesulfonamide
-| image = Sulfisomidine.svg
+| image = Sulfisomidine.png
-| image2 = Sulfisomidine ball-and-stick.png
+| image2 = Sulfisomidine_ball-and-stick.png
 <!--Clinical data-->
@@ Line 55: / Line 55: @@
 | StdInChIKey = YZMCKZRAOLZXAZ-UHFFFAOYSA-N
 }}
+                     __NOTOC__
+{{SI}}
+{{CMG}}
+==Overview==
 '''Sulfisomidine''' ([[International Nonproprietary Name|INN]]), also known as '''sulphasomidine''' ([[British Approved Name|BAN]] until 2003),<ref>
 {{PDFlink|[http://web.archive.org/web/20050827062201/medicines.mhra.gov.uk/inforesources/productinfo/banslist.pdf  Changing substance names from BANs to rINNs.]|34.5&nbsp;[[Kibibyte|KiB]]<!-- application/pdf, 35419 bytes -->}}. [[United Kingdom]] [[Medicines and Healthcare products Regulatory Agency]] (December 12, 2003). Retrieved on 2007-08-26 through [[Archive.org]].</ref> '''sulfamethin''' and '''sulfaisodimidine''', is a [[sulfonamide (medicine)|sulfonamide]] [[antibacterial]]. It is closely related to [[sulfadimidine]].
 ==References==
-{{Reflist}}
+{{Reflist|2}}
 ==External links==
@@ Line 68: / Line 73: @@
 [[Category:Sulfonamide antibiotics]]
 [[Category:Pyrimidines]]
+[[Category:Drug]]
-{{antibiotic-stub}}

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^N
PubChem CID	5343
ChemSpider	5150^Y
UNII	W03L3ODK6E
KEGG	D01526^Y
ChEBI	CHEBI:32166^Y
ChEMBL	ChEMBL485696^Y
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C₁₂H₁₄N₄O₂S
Molar mass	278.331 g/mol
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)^Y Key:YZMCKZRAOLZXAZ-UHFFFAOYSA-N^Y
^NY (what is this?) (verify)

Sulfisomidine: Difference between revisions

Latest revision as of 13:06, 15 April 2015

Overview

References

External links

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