Etorphine
Legal status | |
---|---|
Legal status | |
Identifiers | |
| |
CAS Number | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C25H33NO4 |
Molar mass | 411.53 g/mol |
WikiDoc Resources for Etorphine |
Articles |
---|
Most recent articles on Etorphine |
Media |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Etorphine at Clinical Trials.gov Clinical Trials on Etorphine at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Etorphine
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Etorphine Discussion groups on Etorphine Directions to Hospitals Treating Etorphine Risk calculators and risk factors for Etorphine
|
Healthcare Provider Resources |
Causes & Risk Factors for Etorphine |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
Overview
Etorphine (Immobilon® or M99) is a semi-synthetic opioid possessing an analgesic potency approximately 1000-3000 times that of morphine depending on the test. It was invented in 1963 by a research group at McFarlan-Smith and Co. in Edinburgh, led by Professor Kenneth Bentley.[1][2] It can be produced from thebaine. It is most often used to immobilize elephants and other large mammals. Etorphine is only available legally for veterinary use and is strictly governed by law. Diprenorphine (M5050) is an opioid receptor antagonist that can be administered in proportion to the amount of etorphine used (1.3 times) to reverse its effects. Veterinary-strength etorphine is fatal to humans; one drop on the skin can cause death within a few minutes.[3]
Large Animal Immobilon is a combination of etorphine plus acepromazine maleate. An etorphine antidote Large Animal Revivon contains mainly diprenorphine for animals and a human-specific naloxone-based antidote, which should be prepared prior to the etorphine.
A close relative, dihydroetorphine has been used as opiate painkiller for human usage in China. It is claimed to be less addictive than traditional opioids but this has yet to be confirmed.
Pharmacology
Etorphine is an agonist at <math>\mu</math>, <math>\delta</math>, and <math>\kappa</math> opioid receptors. It also has a weak affinity for the ORL1 nociceptin/orphanin FQ receptor.[4]
Legal status
In Hong Kong, Etorphine is regulated under Schedule 1 of Hong Kong's Chapter 134 Dangerous Drugs Ordinance. It can only be used legally by health professionals and for university research purporses. The substance can be given by pharmacists under a prescription. Anyone who supplies the substance without prescription can be fined $10000(HKD). The penalty for trafficking or manufacturing the substance is a $5,000,000 (Hong Kong dollar) fine and life imprisonment. Possession of the substance for consumption without license from the Department of Health is illegal with a $1,000,000 (HKD) fine and/or 7 years of jail time.
In the Netherlands, Etorphine is a list I drug of the Opium Law. It is only used for veterinary purposes in zoo's to inmobilise large animals.
In the US, Etorphine is listed as a Schedule I drug, although Etorphine hydrochloride is classified as Schedule II.
In popular culture
Etorphine is the drug which the main character in the books and TV-series about the serial killer and blood spatter specialist Dexter uses to immobilize his victims. In one episode of the TV-series it is shown that the character uses a fake doctor's name to obtain the controlled substance.
References
- ↑ Bentley KW, Hardy DG. "New potent analgesics in the morphine series." Proceedings of the Chemical Society. 1963;220.
- ↑ Bentley KW, Hardy DG. "Novel analgesics and molecular rearrangements in the morphine-thebaine group. 3. Alcohols of the 6,14-endo-ethenotetrahydrooripavine series and derived analogs of N-allylnormorphine and -norcodeine." Journal of the American Chemical Society. 1967 Jun 21;89(13):3281-92. PMID 6042764
- ↑ Zoo Vet At Large - Sky Travel (8 July 2007, Part 10 of 26)
- ↑ Hawkinson JE, Acosta-Burruel M, Espitia SA. "Opioid activity profiles indicate similarities between the nociceptin/orphanin FQ and opioid receptors." European Journal of Pharmacology. 2000 Feb 18;389(2-3):107-14. PMID 10688973
External links
- Opioids.com page on etorphine
- Etorphine: Molecule of the Month
- Pages with script errors
- Drugs with non-standard legal status
- E number from Wikidata
- ECHA InfoCard ID from Wikidata
- Chemical articles with unknown parameter in Infobox drug
- Infobox drug articles without a structure image
- Articles without EBI source
- Chemical pages without ChemSpiderID
- Chemical pages without DrugBank identifier
- Articles without KEGG source
- Articles without InChI source
- Articles without UNII source
- Drugs missing an ATC code
- Articles containing unverified chemical infoboxes
- Semisynthetic opioids
- Mu-opioid agonists
- Opioids
- Drugs