Chlormezanone

"Trancopal" redirects here. For Trancopal Dolo, see Flupirtine.

Chlormezanone

Systematic (IUPAC) name
2-(4-chlorophenyl)-3-methyl-1,1-dioxo-1,3-thiazinan-4-one
Clinical data
AHFS/Drugs.com	International Drug Names
Pregnancy cat.	?
Legal status	℞ Prescription only
Routes	Oral
Pharmacokinetic data
Half-life	40.5 hours
Identifiers
CAS number	80-77-3 Y
ATC code	M03BB02
PubChem	CID 2717
DrugBank	APRD00865
ChemSpider	2616 Y
UNII	GP568V9G19 Y
KEGG	D00268 Y
ChEBI	CHEBI:3619 Y
ChEMBL	CHEMBL1200714 N
Chemical data
Formula	C11H12ClNO3S
Mol. mass	273.737 g/mol
SMILES	eMolecules & PubChem
InChI InChI=1S/C11H12ClNO3S/c1-13-10(14)6-7-17(15,16)11(13)8-2-4-9(12)5-3-8/h2-5,11H,6-7H2,1H3 Y Key:WEQAYVWKMWHEJO-UHFFFAOYSA-N Y
N(what is this?)  (verify)

Chlormezanone (marketed under the brandname Trancopal) is a drug used as an anxiolytic and a muscle relaxant.

Its use was discontinued in many countries in 1996, due to rare but serious cases of toxic epidermal necrolysis.

Chemistry

• Sterling Drug Inc., US 3082209  (1958).
• Surrey, A. R.; Webb, W. G.; Gesler, R. M. (1958). "Central Nervous System Depressants. The Preparation of Some 2-Aryl-4-metathiazanones". Journal of the American Chemical Society 80 (13): 3469. doi:10.1021/ja01546a065. 

References

• Wollina U, Hipler U, Seeling A, Oelschlager H (2005). "Investigations of interactions of chlormezanone racemate and its enantiomers on human keratinocytes and human leucoytes in vitro". Skin Pharmacol Physiol 18 (3): 132–138. doi:10.1159/000084910. PMID 15897685. 
• Seeling A, Oelschläger H, Rothley D (2000). "Important pharmaceutical-chemical characteristics of the central muscle relaxant chlormezanone". Pharmazie 55 (4): 293–6. PMID 10798243. 
• Oelschläger H, Klinger W, Rothley D, Seeling A, Bockhard H, Hofmann B, Machts H, Riederer H, Rackur H (1998). "[Cleavage and biotransformation of the central muscle relaxant chlormezanone]". Pharmazie 53 (9): 620–4. PMID 9770210. 
• Gautier V, Vincon G, Demotes-Mainard F, Albin H (1990). "[Pharmacokinetics of chlormezanone in healthy volunteers] (original in French)". Pharmazie 45 (4): 315–9. PMID 2399514.