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- Q15410160 subject Q8887197.
- Q15410160 subject Q8949762.
- Q15410160 abstract "3,14-Diacetyloxymorphone is an opioid analgesic which has never been marketed. It is an acetyl derivative of oxymorphone. It is related to other acetylated morphone derivatives, including 3,6-diacetyloxymorphone, 3,8,14-triacetyloxymorphone, 3,6,8,14-tetraacetyloxymorphone, noroxymorphone analogs of all or most of the above, and 3,6,14-triacetyloxymorphone, a derivative of oxymorphone whose structure-activity relationship suggests is 800 per cent the potency of the parent drug versus 250 per cent for 3,14-diacetyoxymorphone. Both were developed in Austria in the 1920s along with other derivatives of the strong dihydromorphinones and these drugs are generated by reacting oxymorphone with either acetic anhydride or acetyl chloride at various temperatures in the 80-160 °C for several hours; 3,6,14-triacetyloxymorphone may be more easily made when a catalylst is used but elevated pressure or reaction in vacuo or under a nitrogen or noble gas atmosphere is not required. Each of the acetyl esters of oxymorphone has a hydromorphone analogue, and these were all developed around the same time (1915-1930) in Austria and Germany.As an ester of oxymorphone, it is presumably a Schedule II controlled substance as it and its relatives save acetlmorphone do not specifically appear in Schedule I. 3,14-Diacetyloxymorphone and its relatives including acetylmorphone do not, however, have annual production quotas published by the DEA in the Federal Register.Like all or most of the direct morphine derivatives, halogenated derivatives of these drugs and their hydromorphone and hydromorphinol analogues were synthesized in the 1930s when both the esters and the halogenated morphine derivatives were being developed, including one given as 1,2-iodo-3,6,14-triacetyl-6ɑ-14β-hydroxydihydromorphinone in a footnote to a 1948 German medical journal article about the esters of morphine. It appears that this drug was used, labelled with Iodine 129, as a tracer in animal studies, was significantly stronger than morphine, and possibly has 1- and/or 2- fluoro, chloro, and bromo analogues.3,6-Diacetyloxymorphone is a third acetylated oxymorphone derivative, the oxymorphone analogue of acetylmorphone and expected to be intermediate in strength betwixt the two aforementioned drugs. Another is 3-acetyloxymorphone. All of the above have been, owing to their somewhat sophisticated yet straightforward synthesis from pharmaceutical opioids, consistently if in vanishingly small quantities since at least the 1960s by law enforcement around the world as the results of clandestine synthesis, and acetylmorphone itself was banned by the League of Nations in 1930 to prevent its use as a legal heroin substitute. Therefore all or most of this group and its hydromorphone analogues along with some others more closely related to heroin such as acetylpropionylmorphine were the first designer drugs in the 1920s.".
- Q15410160 iupacName "(4R,4aS,7aR,12bS)-3-Methyl-7-oxo-2,3,4,4a,5,6,7,7a-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,9-diyl diacetate".
- Q15410160 thumbnail 3,14-Diacetyloxymorphone.svg?width=300.
- Q15410160 wikiPageWikiLink Q1200715.
- Q15410160 wikiPageWikiLink Q15410157.
- Q15410160 wikiPageWikiLink Q173235.
- Q15410160 wikiPageWikiLink Q303646.
- Q15410160 wikiPageWikiLink Q423380.
- Q15410160 wikiPageWikiLink Q427523.
- Q15410160 wikiPageWikiLink Q4673314.
- Q15410160 wikiPageWikiLink Q4673318.
- Q15410160 wikiPageWikiLink Q481808.
- Q15410160 wikiPageWikiLink Q5955182.
- Q15410160 wikiPageWikiLink Q8887197.
- Q15410160 wikiPageWikiLink Q8949762.
- Q15410160 wikiPageWikiLink Q898317.
- Q15410160 iupacname "-3".
- Q15410160 type ChemicalCompound.
- Q15410160 type ChemicalSubstance.
- Q15410160 type ChemicalObject.
- Q15410160 type Thing.
- Q15410160 type Q11173.
- Q15410160 comment "3,14-Diacetyloxymorphone is an opioid analgesic which has never been marketed. It is an acetyl derivative of oxymorphone.".
- Q15410160 label "3,14-Diacetyloxymorphone".
- Q15410160 depiction 3,14-Diacetyloxymorphone.svg.