Sulforidazine

Sulforidazine
Systematic (IUPAC) name
	10-[2-(1-methylpiperidin-2-yl)ethyl]-2-(methylsulfonyl)-10H-phenothiazine
Clinical data
Pregnancy cat.	?
Legal status	?
Identifiers
CAS number	14759-06-9
ATC code	None
PubChem	CID 31765
ChemSpider	29458
UNII	B7599I244X
Chemical data
Formula	C21H26N2O2S2
Mol. mass	402.575 g/mol
SMILES	eMolecules & PubChem
	InChI InChI=1S/C21H26N2O2S2/c1-22-13-6-5-7-16(22)12-14-23-18-8-3-4-9-20(18)26-21-11-10-17(15-19(21)23)27(2,24)25/h3-4,8-11,15-16H,5-7,12-14H2,1-2H3 ; Key:FLGCRGJDQJIJAW-UHFFFAOYSA-N ;
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Sulforidazine (Imagotan, Psychoson, Inofal) a typical antipsychotic and a metabolite of thioridazine; it and mesoridazine are more potent than the parent compound, whose pharmacological effects are believed by some to be largely due to its metabolism into sulforidazine and mesoridazine.^[1]

[edit] References

^ Niedzwiecki DM, Mailman RB, Cubeddu LX (March 1984). "Greater potency of mesoridazine and sulforidazine compared with the parent compound, thioridazine, on striatal dopamine autoreceptors". Journal of Pharmacology & Experimental Therapeutics 228 (3): 636–9. PMID 6707914.

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[0] Niedzwiecki DM, Mailman RB, Cubeddu LX (March 1984). "Greater potency of mesoridazine and sulforidazine compared with the parent compound, thioridazine, on striatal dopamine autoreceptors". Journal of Pharmacology & Experimental Therapeutics 228 (3): 636–9. PMID 6707914.

[1]

Jan	FEB	Mar
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2011	2012	2013

Sulforidazine

[edit] References

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