# Pseudomorphine

> Mediated Wiki article. Canonical URL: https://mediated.wiki/source/Pseudomorphine
> Markdown URL: https://mediated.wiki/source/Pseudomorphine.md
> Source: https://en.wikipedia.org/wiki/Pseudomorphine
> Source revision: 1330457771
> License: Creative Commons Attribution-ShareAlike 4.0 International (https://creativecommons.org/licenses/by-sa/4.0/)

{{Redirect-distinguish|Dehydromorphine|dihydromorphine}}
{{Chembox
| ImageFile = Pseudomorphine skeletal.svg
| ImageClass = skin-invert-image
| ImageFile_Ref = {{chemboximage|correct|??}}
| ImageName = 
| IUPACName = (5α,6α)-2-[(5α,6α)-3,6-dihydroxy-17-methyl-7,8-didehydro-4,5-epoxymorphinan-2-yl]-17-methyl-7,8-didehydro-4,5-epoxymorphinan-3,6-diol
|Section1={{Chembox Identifiers
| Abbreviations = 2,2'-bimorphine<ref name=bentley/>
| CASNo =  125-24-6
| CASNo_Ref = {{cascite|correct|??}}
| UNII = AEZ78QX2G7
| PubChem = 234570
| ChemSpiderID = 4590027
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| EINECS = 
| KEGG = 
| KEGG_Ref = {{keggcite|correct|kegg}}
| SMILES = CN1CCC23C4C1CC5=C2C(=C(C(=C5)C6=CC7=C8C(=C6O)OC9C81CCN(C(C7)C1C=CC9O)C)O)OC3C(C=C4)O
| StdInChI = 1S/C34H36N2O6/c1-35-9-7-33-19-3-5-23(37)31(33)41-29-25(33)15(13-21(19)35)11-17(27(29)39)18-12-16-14-22-20-4-6-24(38)32-34(20,8-10-36(22)2)26(16)30(42-32)28(18)40/h3-6,11-12,19-24,31-32,37-40H,7-10,13-14H2,1-2H3
| StdInChIKey = FOJYFDFNGPRXDR-UHFFFAOYSA-N
}}
|Section2={{Chembox Properties
| C=34 | H=36 | N=2 | O=6 
}}
}}

'''Pseudomorphine''' (also known as '''oxydimorphine''' or '''dehydromorphine''') is an inactive, natural [dimerisation](/source/Dimer_(chemistry)) product of the [morphine](/source/morphine) molecule in tandem and thus a common impurity in morphine concentrations. It was first described by Pelletier in 1835.<ref>{{cite journal | author = A. K. Balls | title = Concerning Pseudomorphine | journal = Journal of Biological Chemistry | year = 1927 | volume = 71 | issue = 2 | pages = 537–542 | doi = 10.1016/S0021-9258(18)84438-6 | url = http://www.jbc.org/content/71/2/537 | doi-access = free }}</ref>

This compound may be synthesized by the [oxidative coupling](/source/oxidative_coupling) of [morphine](/source/morphine) by [potassium ferricyanide](/source/potassium_ferricyanide).<ref name=bentley>{{cite journal | title = 512. The structure of pseudomorphine | year = 1959 | last1 = Bentley | first1 = K. W. | last2 = Dyke | first2 = S. F. | journal = Journal of the Chemical Society (Resumed) | volume = 1959 | pages = 2574–2577 | doi = 10.1039/JR9590002574 }}</ref>

Pseudomorphine contributes very little to morphine's effects. It produces no effects in the central nervous or gastrointestinal systems, but it might have some effects on the circulatory system.<ref>{{Cite journal|last1=Schmidt|first1=Carl F.|last2=Livingston|first2=A. E.|date=1933-04-01|title=A Note Concerning the Actions of Pseudomorphine|url=http://jpet.aspetjournals.org/content/47/4/473|journal=Journal of Pharmacology and Experimental Therapeutics|language=en|volume=47|issue=4|pages=473–485|issn=0022-3565}}</ref>

==See also==
*[Thebaine](/source/Thebaine) (paramorphine)
*[Morphine-N-oxide](/source/Morphine-N-oxide)
*[Morphine-3-glucuronide](/source/Morphine-3-glucuronide)
*[Morphine-6-glucuronide](/source/Morphine-6-glucuronide)

==References==
{{Reflist|2}}

{{Components of Opium}}

Category:4,5-Epoxymorphinans

{{analgesic-stub}}

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Adapted from the Wikipedia article [Pseudomorphine](https://en.wikipedia.org/wiki/Pseudomorphine) by Wikipedia contributors ([contributor history](https://en.wikipedia.org/wiki/Pseudomorphine?action=history)). Available under [Creative Commons Attribution-ShareAlike 4.0 International](https://creativecommons.org/licenses/by-sa/4.0/). Changes may have been made.