Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

Jump to content

GD-42

From Wikipedia, the free encyclopedia
GD-42
Names
Preferred IUPAC name
4,8-Dimethyl-4-oxo-3-oxa-5,8-dithia-4λ5-phosphadecan-8-ium methyl sulfate
Other names
Methylsulfomethylate
Identifiers
3D model (JSmol)
ChemSpider
  • 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-1
    Key: AUACWHVUVIIDOR-UHFFFAOYSA-M
  • CCOP(=O)(C)SCC[S+](C)CC.COS(=O)(=O)[O-]
Properties
C9H23O6PS3
Molar mass 354.43 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

GD-42 (methylsulfomethylate) is an irreversible acetylcholinesterase inhibitor.[1][2] It has a positively charged sulfonium group.

See also

[edit]

References

[edit]
  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.