Ethylmethylthiambutene: Difference between revisions
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Latest revision as of 20:53, 16 March 2025
Ethylmethylthiambutene is a synthetic opioid that is part of the thiambutene family. It is a potent analgesic drug, several times stronger than morphine.
Chemistry[edit]
Ethylmethylthiambutene is a chemical compound with the formula C15H23NS. It is a derivative of thiambutene, which is a series of opioid drugs synthesized in the 1950s. The chemical structure of ethylmethylthiambutene is similar to other opioids, with a core structure of a phenylpiperidine moiety. This structure is responsible for the drug's analgesic properties.
Pharmacology[edit]
The pharmacological action of ethylmethylthiambutene is primarily due to its agonist activity at the mu-opioid receptor. This receptor is a G-protein coupled receptor that mediates the pain-relieving effects of opioids. Ethylmethylthiambutene binds to the mu-opioid receptor, causing a conformational change that leads to the inhibition of an intracellular enzyme called adenylate cyclase. This inhibition decreases the levels of cyclic adenosine monophosphate (cAMP) in the cell, leading to a decrease in pain sensation.
Medical Use[edit]
Ethylmethylthiambutene is used in the treatment of severe pain. Due to its potency, it is typically reserved for use in patients who have not responded to other, less potent opioids. Like other opioids, ethylmethylthiambutene has the potential for abuse and dependence, and its use is strictly controlled under the Controlled Substances Act.
Side Effects[edit]
The side effects of ethylmethylthiambutene are similar to those of other opioids and can include nausea, vomiting, constipation, and respiratory depression. In addition, long-term use can lead to physical dependence and withdrawal symptoms upon cessation of use.
See Also[edit]
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Ethylmethylthiambutene
