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GD-42

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Chemical compound
GD-42
Names
Preferred IUPAC name 4,8-Dimethyl-4-oxo-3-oxa-5,8-dithia-4λ-phosphadecan-8-ium methyl sulfate
Other names Methylsulfomethylate
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C8H20O2PS2.CH4O4S/c1-5-10-11(3,9)12-7-8-13(4)6-2;1-5-6(2,3)4/h5-8H2,1-4H3;1H3,(H,2,3,4)/q+1;/p-1Key: AUACWHVUVIIDOR-UHFFFAOYSA-M
SMILES
  • CCOP(=O)(C)SCC(C)CC.COS(=O)(=O)
Properties
Chemical formula C9H23O6PS3
Molar mass 354.43 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

GD-42 (methylsulfomethylate) is an irreversible acetylcholinesterase inhibitor. It has a positively charged sulfonium group.

See also

References

  1. Danilov, AF; Kvitko, IJ; Lavrentieva, VV; Michelson, MJ; Porai-Koshits, BA; Rozhkova, EK; Shelkovnikov, SA (April 1972). "Action of some bisquaternary derivatives of phthalic acids and related substances on neuromuscular transmission". British Journal of Pharmacology. 44 (4): 765–78. doi:10.1111/j.1476-5381.1972.tb07314.x. PMC 1665980. PMID 4339387.
  2. Danilov, AF; Ivanov, YJ; Michelson, MJ (January 1976). "The influence of motor nerve tetanization on the effect of organophosphorus cholinesterase inhibitors on neuromuscular transmission". British Journal of Pharmacology. 56 (1): 115–23. doi:10.1111/j.1476-5381.1976.tb06966.x. PMC 1666757. PMID 175873.
Acetylcholine metabolism and transport modulators
Enzyme
(modulators)
ChATTooltip Choline acetyltransferase
AChETooltip Acetylcholinesterase
BChETooltip Butyrylcholinesterase
Transporter
(modulators)
CHTTooltip Choline transporter
VAChTTooltip Vesicular acetylcholine transporter
Release
(modulators)
Inhibitors
Enhancers
See also
Receptor/signaling modulators
Muscarinic acetylcholine receptor modulators
Nicotinic acetylcholine receptor modulators
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