Decamethonium iodide

Frog rectus abdominis Membrane depolarization Decamethonium iodide (not a receptor-mediated activity) Bums and Paton, 1951... 

Starting with this hypothetical structure-activity relationship, the syntheses and biological investigations of 210-215 and decamethonium iodide were carried out130,13 U As an example, the synthesis of 212 is described in Scheme 26. The pharmacological and toxicological data are given in Table 20 and Table 21, respectively. 

Overdoses of 210-215 lead to death because of respiratory paralysis. The LDS0 values are very low (see Table 21) and all compounds are even more toxic than the standard decamethonium iodide. In addition, the most toxic agent 212, which is nearly 30 times more toxic than the standard decamethonium iodide, seems to be the most toxic organosilicon compound described in the literature up to now. 

Deca-Durabolin" nandrolone. decamethonium bromide decamethonium iodide. 

Syncurine decamethonium iodide, syndyphalin (Syndyphalin 33) is a synthetic pseudopeptide enkephalin analogue, and is an OPIOID RECEPTOR AGONIST with OPIOID ANALGESIC activity, syndyphalin 25 (SD 25) is a synthetic pseudopeptide enkephalin analogue, and is a (p) opioid RECEPTOR AGONIST with OPIOID ANALGESIC activity. 

Decamethonium iodide (150) is the most prominent and most effective neuromuscular blocking agent in the series of a,cu-polymethylenebisammonium iodides of the type 151. 

C3H< N 75-50-3) see Acetylcholine chloride Betaine hydrate Bethanechol chloride Carbachol Carnitine Cetrimonium bromide Choline chloride Choline hydroxide Decamethonium bromide Hexcarbacholine bromide Miltefosine Prolonium iodide... 

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