Chemistry:Gallamine triethiodide
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| Trade names | Flaxedil |
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| Formula | C30H60N3O3+3 · 3 I− (gallamine triethiodide) C24H45N3O3 (gallamine) |
| Molar mass | 891.529 g/mol (gallamine triethiodide) 423.633 g/mol (gallamine) |
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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 is a non-depolarising type of blocker as it binds to the acetylcholine receptor but does not have the biological activity of acetyl choline. 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.[citation needed]
Presence of iodine makes it radio opaque, and its ampule in a bag at airport's x-ray scanner raise the false suspicion of a bullet in the bag.
Gallamine triethiodide was commonly used to prevent muscle contractions during surgical procedures, but now superseded by new neuromuscular blocking drugs with less side effects.
It was developed by Daniel Bovet in 1947.[5]
The drug is no longer marketed in the United States, according to the FDA Orange Book.
See also
References
- ↑ "Webster's Online Dictionary - Flaxedil". http://www.websters-online-dictionary.org/Fl/Flaxedil.html.[yes|permanent dead link|dead link}}]
- ↑ "RxMed: Pharmaceutical Information - FLAXEDIL". http://www.rxmed.com/b.main/b2.pharmaceutical/b2.1.monographs/CPS-%20Monographs/CPS-%20(General%20Monographs-%20F)/FLAXEDIL.html.
- ↑ "[Studies on the causes of gallamine tachycardia and its antagonistic modification by beta adrenolytics]" (in de). Der Anaesthesist 14 (10): 298–301. October 1965. PMID 4380161.
- ↑ "Ventricular tachycardia with gallamine and cyclopropane anesthesia". Anesthesiology 24: 119. 1963. doi:10.1097/00000542-196301000-00024. PMID 13998750.
- ↑ "Neuromuscular blocking drugs: discovery and development". Journal of the Royal Society of Medicine 95 (7): 363–7. July 2002. doi:10.1177/014107680209500713. PMID 12091515. PMC 1279945. http://www.jrsm.org/cgi/pmidlookup?view=long&pmid=12091515.
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