Gallamine triethiodide

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Gallamine triethiodide
File:Gallamine triethiodide.svg
Systematic (IUPAC) name
2,2’,2’’-[benzene-1,2,3-triyltris(oxy)]tris(N,N,N-triethylethanaminium) triiodide
Clinical data
Trade names Flaxedil
AHFS/Drugs.com International Drug Names
Identifiers
CAS Number 65-29-2 YesY
ATC code M03AC02 (WHO)
PubChem CID: 6172
IUPHAR/BPS 356
DrugBank DB00483 YesY
ChemSpider 5937 N
UNII Q3254X40X2 YesY
KEGG D02292 YesY
ChEBI CHEBI:503442 YesY
ChEMBL CHEMBL1200993 N
Chemical data
Formula C30H60N3O3+3 · 3 I (gallamine triethiodide)
C24H45N3O3 (gallamine)
Molecular mass 891.529 g/mol (gallamine triethiodide)
423.633 g/mol
(gallamine)
  • [I-].[I-].[I-].O(c1c(OCC[N+](CC)(CC)CC)cccc1OCC[N+](CC)(CC)CC)CC[N+](CC)(CC)CC
  • InChI=1S/C24H45N3O3/c1-7-25(8-2)16-19-28-22-14-13-15-23(29-20-17-26(9-3)10-4)24(22)30-21-18-27(11-5)12-6/h13-15H,7-12,16-21H2,1-6H3 YesY
  • Key:ICLWTJIMXVISSR-UHFFFAOYSA-N YesY
 NYesY (what is this?)  (verify)

Gallamine triethiodide (Flaxedil) is a non-depolarising muscle relaxant.[1] It acts by combining with the cholinergic receptor sites in muscle and competitively blocking the transmitter action of acetylcholine.[2] Gallamine triethiodide has a parasympatholytic effect on the cardiac vagus nerve which causes tachycardia[3][4] and occasionally hypertension. Very high doses cause histamine release.

Gallamine triethiodide is commonly used to stabilize muscle contractions during surgical procedures.

It was developed by Daniel Bovet in 1947.[5]

The pharmaceutical is no longer marketed in the United States, according to the FDA Orange Book.

File:Flaxedil.png
An ampoule of gallamine.

References

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