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Soman, or GD (systematic name: O-Pinacolyl methylphosphonofluoridate), is an extremely toxic chemical substance. It is a nerve agent, interfering with normal functioning of the mammalian nervous system by inhibiting the cholinesterase enzyme. It is an inhibitor of both acetylcholinesterase and butyrylcholinesterase.[1] As a chemical weapon, it is classified as a weapon of mass destruction by the United Nations according to UN Resolution 687. Its production is strictly controlled, and stockpiling is outlawed by the Chemical Weapons Convention of 1993 where it is classified as a Schedule 1 substance. Soman was the third of the so-called G-series nerve agents to be discovered along with GA (tabun), GB (sarin), and GF (cyclosarin).
It is a volatile, corrosive, and colorless liquid with a faint odor when pure. More commonly, it is a yellow to brown color and has a strong odor described as similar to camphor. The LCt50 for soman is 70 mg·min/m3 in humans. It is both more lethal and more persistent than sarin or tabun, but less so than cyclosarin.
GD can be thickened for use as a chemical spray using an acryloid copolymer. It can also be deployed as a binary chemical weapon; its precursor chemicals are methylphosphonyl difluoride and a mixture of pinacolyl alcohol and an amine.
Contents
History
After World War I, in which mustard agent and phosgene were used as chemical warfare agents, the Geneva protocol (1925) was signed in an attempt to ban chemical warfare. Nevertheless, research into chemical warfare agents and the use of them continued. It wasn’t until 1936 before new, more dangerous chemical agents were discovered: Gerhard Schrader (I.G. Farben, Germany) isolated Tabun (named GA for German Agent A by the United States) the first nerve agent while developing new insecticides. This discovery was followed by the isolation of sarin (designated GB by the United States) in 1938, also discovered by Schrader.During World War II the research into nerve agents continued in the United States and Germany. In 1944, soman, a colorless liquid with a camphor odor, (designated GD by the United States) was developed by the Germans. Soman proved to be even more toxic than tabun and sarin. Nobel Laureate Richard Kuhn discovered soman during research into the pharmacology of tabun and sarin. This research was commissioned by the German Army. Although soman was produced and stored by the Germans, it was never used in World War II, just like tabun and sarin were never used as chemical warfare agents.[2]:10-13
The crystal structure of soman complexed with acetylcholinesterase was determined by Millard et al. (1999) by X-ray crystallography.[3]
Structure and reactivity
Soman has a phosphonyl group with a fluoride and a (large) hydrocarbon covalently bound to it. The structure is therefore similar like sarin; which only has a smaller hydrocarbon group attached (isopropyl). Because of the similarity between the chemical structures, the reactivity of both toxins is (almost) the same. Soman and Sarin will both react by using the phospho oxygen group; which can bind to amino acids, like Serine.Synthesis
The manufacture of soman is very similar to the manufacture of sarin. The difference is that the isopropanol from the sarin processes is replaced with pinacolyl alcohol:
The synthesis of soman from pinacolyl alcohol
Available forms
Soman is a liquid under standard conditions with a somewhat fruity aroma. On the battlefield, it is nebulized and thus not a gaseous substance. Soman has four stereo isomers, each with a different toxicity, though largely similar.Mechanisms of action
Soman is an organophosphorous nerve agent with a mechanism of action similar to Tabun. Nerve agents inhibit acetylcholine esterase (AChE) by forming an adduct with the enzyme via a serine residue on that enzyme. These adducts may be decomposed hydrolytically or, for example, by the action of some oximes and thereby regenerate the enzyme. A second reaction type, one in which the enzyme–organophosphate (OP) complex undergoes a subsequent reaction, is usually described as ‘‘aging’’. Once the enzyme–OP complex has aged it is no longer regenerated by the common, oxime reactivators. The rate of this process is dependant on the OP. Soman is an OP that stimulates the rate of aging most rapidly decreasing the half-life to just a few minutes.AChE is an enzyme involved with neurotransmission. Because of the severe decrease of the half-life of this enzyme, neurotransmission is abolished in a matter of minutes.[2]
Metabolism
Once taken up in the human body, soman doesn’t only inhibit AChE, but it is also a substrate for other esterases. Reaction of soman with these esterases allows for the detoxication of the compound. No metabolic toxification reactions are known for soman.Soman can be hydrolyzed by a so-called A-esterase, more specific a diisopropylfluorophosphatase. This esterase, also called somanase, reacts with the anhydride bond between phosphorus and fluorine and accounts for the hydrolysis of the fluoride. Somanase also hydrolyses the methyl group of soman resulting in the formation of pinacolyl methylphosphonic acid (PMPA), which is a less potent AChE inhibitor.
Soman can also bind to other esterases, e.g., AChE, cholinesterase (ChE) and carboxylesterases (CarbE). In this binding, soman loses its fluoride. After binding to AChE or ChE soman also loses its phosphoryl group, leading to the formation of methylphosphonic acid (MPA). Binding to CarbE reduce the total concentration of soman in the blood, thus resulting in a lower toxicity. Furthermore, CarbE are involved in the detoxication by hydrolysing soman to PMPA. So CarbE account for the detoxication of soman in two ways.[4][5]
The importance of the detoxication of soman after exposure was illustrated in experiments of Fonnum and Sterri (1981). They reported that only 5% of LD50 inhibited AChE in rats, resulting in acute toxic effects. This shows that metabolic reactions accounted for the detoxification of the remaining 95% of the dose.[6]
The metabolisim of soman
Indications
As Soman is closely related to compounds such as Sarin, indications for a Soman poisoning are relatively similar. One of the first observable signs of a soman poisoning is miosis. Some, but not all of the later indications are vomiting, extreme muscle pain and peripheral nervous system problems. Those symptoms show as fast as 10 minutes after exposure and may last for many days.[7]Toxicity and efficacy
Soman is a very effective compound that has severe health implications at very low doses. The LC50 of soman in air is 70 mg min per m3. For compounds such as soman, which may also be used as a weapon, often a fraction of the LC50 dose is where the first effects appear. Miosis, is one of the first symptoms of soman intoxication and can be seen in doses of less than 1% of the LC50.[8]By using animal models, it is able to predict the LD50 value of soman. Table 1 [9][10] shows LD50 values of several exposed organisms via different administration routes. Most LD50 values via the same administration route give somewhat different lethal doses, which means the organisms metabolize the compounds differently.
Side effects
Except for the direct toxic effects concerning the nervous system, people exposed to soman might experience some long term effects, most of which are psychological.People that were exposed to a very little dose of soman suffered severe toxic effects, once those were treated and long gone the same persons often developed a depression, admitted they had antisocial thoughts, were withdrawn and subdued, slept restlessly and had bad dreams. Those symptoms lasted until half a year after exposure but left without any lifelong damages.[7]
Effects on animals
Experiments have been done in which rats were exposed to soman to test if behavioral effects could be seen at low doses without generating overt symptoms. Exposure of the rats to soman in a dose of less than 3 percent of the LD50 caused alterations of the behavior. The active avoidance of the exposed rats was less than the avoidance of non-exposed rats (two-way shuttlebox experiment). Also the motor coordination (hurdle-stepping task), open field behavior and active as well as passive avoidance behavior were affected. One can conclude that rats that are exposed to soman performed with less success in tasks that require motor activity as well as the function of higher structures of the central nervous system (CNS) on the same time. In this, soman has a predominantly central effect.The knowledge of the effects of low doses of soman and other choline esterase inhibitors on rats could possibly be used to explain the relatively high incidence of airplane accidents due to errors of agricultural pilots. If this knowledge could be applied to humans, one could explain this high incidence with depressed choline esterase activity due to exposure to pesticides. It is not known whether the extrapolation from rats to humans can be made.[11]
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