Misplaced Pages

Ro4-1539: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editNext edit →Content deleted Content addedVisualWikitext
Revision as of 16:40, 12 September 2011 editPotatoBot (talk | contribs)Bots51,239 editsm Stub sorting and placement of stub template(s): analgesic-stub. See approval. Report errors and suggestions at User talk:PotatoBot.← Previous edit Revision as of 13:40, 23 October 2011 edit undo70.137.143.167 (talk) cite patentNext edit →
Line 39: Line 39:
}} }}


'''Ro4-1539''' ('''Furethylnorlevorphanol''') is an ] ] drug from the ] series, which was developed by the pharmaceutical company ] in the 1950s.<ref>US Patent 2970147</ref> It acts as a potent ] agonist, and was found to be around 30-60x more potent than the related drug ] in animal experiments.<ref></ref><ref>Hellerbach J, Schnider O, Besendorf H, Pellmont B. Synthetic Analgesics. Part IIA. Morphinans. Pergamon Press, 1966.</ref> While it is notable for its high potency, being among the more potent μ-agonist found in the morphinan series of drugs (though not on the scale of ] and other morphinans in the extremity of their level of potency), Ro4-1539 had no particular clinical advantages over other available opioid drugs, and was never commercially marketed. '''Ro4-1539''' ('''Furethylnorlevorphanol''') is an ] ] drug from the ] series, which was developed by the pharmaceutical company ] in the 1950s.<ref>{{cite patent | US | 2970147 }}</ref> It acts as a potent ] agonist, and was found to be around 30-60x more potent than the related drug ] in animal experiments.<ref></ref><ref>Hellerbach J, Schnider O, Besendorf H, Pellmont B. Synthetic Analgesics. Part IIA. Morphinans. Pergamon Press, 1966.</ref> While it is notable for its high potency, being among the more potent μ-agonist found in the morphinan series of drugs (though not on the scale of ] and other morphinans in the extremity of their level of potency), Ro4-1539 had no particular clinical advantages over other available opioid drugs, and was never commercially marketed.


Ro4-1539 has never been formally trialled in humans, but based on its effects in animals it would be expected to produce effects similar to those of other potent opioid agonists, including strong ], ], ], ], ] and also ] which could be harmful or fatal. Ro4-1539 has never been formally trialled in humans, but based on its effects in animals it would be expected to produce effects similar to those of other potent opioid agonists, including strong ], ], ], ], ] and also ] which could be harmful or fatal.




==See also== ==See also==

Revision as of 13:40, 23 October 2011

Pharmaceutical compound
Ro4-1539
Identifiers
IUPAC name
  • 17-(2-(furan-2-yl)ethyl)-3-hydroxymorphinan
CAS Number
PubChem CID
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC22H27NO2
Molar mass337.454 g/mol g·mol
3D model (JSmol)
SMILES
  • C3CCCC1C35c2cc(O)ccc2CC1N(CC5)CCc4ccco4
  (verify)

Ro4-1539 (Furethylnorlevorphanol) is an opioid analgesic drug from the morphinan series, which was developed by the pharmaceutical company Hoffmann–La Roche in the 1950s. It acts as a potent μ-opioid agonist, and was found to be around 30-60x more potent than the related drug levorphanol in animal experiments. While it is notable for its high potency, being among the more potent μ-agonist found in the morphinan series of drugs (though not on the scale of acetorphine and other morphinans in the extremity of their level of potency), Ro4-1539 had no particular clinical advantages over other available opioid drugs, and was never commercially marketed.

Ro4-1539 has never been formally trialled in humans, but based on its effects in animals it would be expected to produce effects similar to those of other potent opioid agonists, including strong analgesia, sedation, euphoria, constipation, itching and also respiratory depression which could be harmful or fatal.

See also

References

  1. US 2970147 
  2. Nathan B. Eddy, Hedwig Besendorf and Béla Pellmont. Synthetic analgesics - Aralkyl substitution on nitrogen of morphinan. UNODC Bulletin on Narcotics 1958 p 23-42.
  3. Hellerbach J, Schnider O, Besendorf H, Pellmont B. Synthetic Analgesics. Part IIA. Morphinans. Pergamon Press, 1966.
Opioid receptor modulators
μ-opioid
(MOR)
Agonists
(abridged;
full list)
Antagonists
δ-opioid
(DOR)
Agonists
Antagonists
κ-opioid
(KOR)
Agonists
Antagonists
Nociceptin
(NOP)
Agonists
Antagonists
Others
  • Others: Kyotorphin (met-enkephalin releaser/degradation stabilizer)


Stub icon

This analgesic-related article is a stub. You can help Misplaced Pages by expanding it.

Categories: