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Thebaine

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Thebaine
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IUPAC names
6,7,8,14-tetradehydro-4,5a-epoxy-
3,6-dimethoxy-17-methylmorphinan
Other names
Paramorphine
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115-37-7 7pxY
ChEBI CHEBI:9519 7pxY
ChEMBL ChEMBL403893 7pxY
ChemSpider 4481822 7pxY
4479543 7pxY
Jmol-3D images Image
KEGG C06173 7pxN
MeSH Thebaine
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C19H21NO3
Molar mass Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). g·mol−1
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Metabolism O-demethylation [1]
Legal status
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Thebaine (paramorphine), also known as codeine methyl enol ether, is an opiate alkaloid, its name coming from the Greek Θῆβαι, Thēbai (Thebes), an ancient city in Upper Egypt. A minor constituent of opium, thebaine is chemically similar to both morphine and codeine, but has stimulatory rather than depressant effects. At high doses, it causes convulsions similar to strychnine poisoning. The synthetic enantiomer (+)-thebaine does show analgesic effects apparently mediated through opioid receptors, unlike the inactive natural enantiomer (−)-thebaine.[3] Thebaine is not used therapeutically, but as the main alkaloid extracted from Papaver bracteatum (Iranian poppy), it can be converted industrially into a variety of compounds including oxycodone, oxymorphone, nalbuphine, naloxone, naltrexone, buprenorphine and etorphine.

Thebaine is controlled under international law, is listed as a Class A drug under the Misuse of Drugs Act 1971 in the United Kingdom, is controlled as an analog of a Schedule II drug per the Analog Act in the United States of America, and is controlled with its derivatives and salts, as a Schedule I substance of the Controlled Drugs and Substances Act in Canada.[4] The 2013 US Drug Enforcement Administration (DEA) aggregate manufacturing quota for thebaine (ACSCN 9333) was unchanged from the previous year at 145 metric tons.

This alkaloid is biosynthetically related to salutaridine, oripavine, morphine and reticuline.[5]

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Morphine biosynthesis


See also

References

  1. ^ Mikus, G.; Somogyi, A. A.; Bochner, F.; Eichelbaum, M. (1991). "Thebaine O-demethylation to oripavine: Genetic differences between two rat strains". Xenobiotica 21 (11): 1501–9. PMID 1763524. doi:10.3109/00498259109044400. 
  2. ^ WHO Advisory Group (1980). "The dependence potential of thebaine". Bulletin on Narcotics 32 (1): 45–54. PMID 6778542. 
  3. ^ Aceto, M. D.; Harris, L. S.; Abood, M. E.; Rice, K. C. (1999). "Stereoselective μ- and δ-opioid receptor-related antinociception and binding with (+)-thebaine". European Journal of Pharmacology 365 (2–3): 143–7. PMID 9988096. doi:10.1016/S0014-2999(98)00862-0. 
  4. ^ "Controlled Drugs and Substances Act". Justice Laws Website. Government of Canada. 2012-11-06. Retrieved 2014-01-12. 
  5. ^ Novak, B.; Hudlicky, T.; Reed, J.; Mulzer, J.; Trauner, D. (2000). "Morphine Synthesis and Biosynthesis-An Update" (PDF). Current Organic Chemistry 4 (3): 343–62. doi:10.2174/1385272003376292. 


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