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Short description : Typical antipsychotic medication
Sulforidazine Clinical data ATC code Identifiers
10-{2-[(RS) -1-Methylpiperidin-2-yl]ethyl}-2-(methylsulfonyl)-10H -phenothiazine
CAS Number PubChem CID ChemSpider UNII ChEBI ChEMBL Chemical and physical data Formula C 21 H 26 N 2 O 2 S 2 Molar mass 402.57 g·mol−1 3D model (JSmol )
O=S(=O)(c2cc1N(c3c(Sc1cc2)cccc3)CCC4N(C)CCCC4)C
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
Y Key:FLGCRGJDQJIJAW-UHFFFAOYSA-N
Y
N Y (what is this?) (verify)
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]
Synthesis
2-bromo-2'-amino-4'-methylsulphonyl-diphenyl Sulphide, CID:43448246 (1 )
2-bromo-2'-acetamino-4'-methylsulphonyl diphenylsulphide (2 )
2-(2-Chloroethyl)-1-Methylpiperidine [50846-01-0] (3 )
References
↑ "Greater potency of mesoridazine and sulforidazine compared with the parent compound, thioridazine, on striatal dopamine autoreceptors". Journal of Pharmacology and Experimental Therapeutics 228 (3): 636–9. March 1984. PMID 6707914 .
↑ Morrow, Ryan J.; Millership, Jeff S.; Collier, Paul S. (2005). "Facile Syntheses of the Three Major Metabolites of Thioridazine". Helvetica Chimica Acta. 88 (5): 962–967. doi:10.1002/hlca.200590089.
↑ FR1363683 idem Bruschweiler Conrad, Schwarb Gustav, Winkler Hans, Renz Jany, U.S. Patent 3,314,948 (1967 to Sandoz Ltd).
mAChRs
Agonists Antagonists
3-Quinuclidinyl benzilate
4-DAMP
Aclidinium bromide (+formoterol )
Abediterol
AF-DX 250
AF-DX 384
Ambutonium bromide
Anisodamine
Anisodine
Antihistamines (first-generation) (e.g., brompheniramine , buclizine , captodiame , chlorphenamine (chlorpheniramine) , cinnarizine , clemastine , cyproheptadine , dimenhydrinate , [[Chemistry:Dimetdimetindene, Diphenhydramine |diphenhydramine]], doxylamine , meclizine , mepyramine (pyrilamine) , mequitazine , perlapine , phenindamine , pheniramine , Phenyltoloxamine|Phenyltoloxamine ]]]], promethazine , propiomazine , triprolidine )
AQ-RA 741
Atropine
Atropine methonitrate
Atypical antipsychotics (e.g., clozapine, Chemistry :Fluperlapine
Precursors (and prodrugs)
nAChRs
Agonists (and PAMs )
5-HIAA
A-84,543
A-366,833
A-582,941
A-867,744
ABT-202
ABT-418
ABT-560
ABT-894
Acetylcholine
Altinicline
Anabasine
Anatoxin-a
AR-R17779
Bephenium hydroxynaphthoate
Butinoline
Butyrylcholine
Carbachol
Choline
Cotinine
Cytisine
Decamethonium
Desformylflustrabromine
Dianicline
Dimethylphenylpiperazinium
Epibatidine
Epiboxidine
Ethanol (alcohol)
Ethoxysebacylcholine
EVP-4473
EVP-6124
Galantamine
GTS-21
Ispronicline
Ivermectin
JNJ-39393406
Levamisole
Lobeline
MEM-63,908 (RG-3487)
Morantel
Nicotine (tobacco )
NS-1738
PHA-543,613
PHA-709,829
PNU-120,596
PNU-282,987
Pozanicline
Pyrantel
Rivanicline
RJR-2429
Sazetidine A
SB-206553
Sebacylcholine
SIB-1508Y
SIB-1553A
SSR-180,711
Suberyldicholine
Suxamethonium (succinylcholine)
Suxethonium (succinyldicholine)
TC-1698
TC-1734
TC-1827
TC-2216
TC-5214
TC-5619
TC-6683
Tebanicline
Tribendimidine
Tropisetron
UB-165
Varenicline
WAY-317,538
XY-4083
Antagonists (and NAMs )
Precursors (and prodrugs)
Original source: https://en.wikipedia.org/wiki/Sulforidazine. Read more