Dextrallorphan

Dextrallorphan
Dextrallorphan
Systematic (IUPAC) name
(+)-(13α,14α)-17-allylmorphinan-3-ol
Clinical data
Pregnancy cat.  ?
Legal status Uncontrolled
Routes Oral
Identifiers
CAS number 5822-43-5
ATC code None
PubChem CID 5748237
ChemSpider 2339009
Chemical data
Formula C19H25NO 
Mol. mass 283.41 g/mol
SMILES eMolecules & PubChem

Dextrallorphan (DXA) is a drug of the morphinan class known in scientific research. It acts as a σ1 receptor agonist, κ-opioid receptor agonist[citation needed], and NMDA receptor antagonist.[1][2][3][4] It has no significant affinity for the σ2, μ-opioid, or δ-opioid receptor, or for the serotonin or norepinephrine transporter.[5][2] As an NMDA receptor antagonist, in vivo, it is approximately twice as potent as dextromethorphan, and five-fold less potent than dextrorphan.[3]

See also

References

  1. ^ Su TP (November 1982). "Evidence for sigma opioid receptor: binding of [3HSKF-10047 to etorphine-inaccessible sites in guinea-pig brain"]. The Journal of Pharmacology and Experimental Therapeutics 223 (2): 284–90. PMID 6290634. http://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=6290634. 
  2. ^ a b Codd EE, Shank RP, Schupsky JJ, Raffa RB (September 1995). "Serotonin and norepinephrine uptake inhibiting activity of centrally acting analgesics: structural determinants and role in antinociception". The Journal of Pharmacology and Experimental Therapeutics 274 (3): 1263–70. PMID 7562497. http://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=7562497. 
  3. ^ a b Shukla VK, Lemaire S (January 1997). "N-methyl-D-aspartate antagonist activity of alpha- and beta-sulfallorphans". The Journal of Pharmacology and Experimental Therapeutics 280 (1): 357–65. PMID 8996216. http://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=8996216. 
  4. ^ Shannon HE (April 1983). "Pharmacological evaluation of N-allynormetazocine (SKF 10,047) on the basis of its discriminative stimulus properties in the rat". The Journal of Pharmacology and Experimental Therapeutics 225 (1): 144–52. PMID 6834266. http://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=6834266. 
  5. ^ He XS, Bowen WD, Lee KS, Williams W, Weinberger DR, de Costa BR (March 1993). "Synthesis and binding characteristics of potential SPECT imaging agents for sigma-1 and sigma-2 binding sites". Journal of Medicinal Chemistry 36 (5): 566–71. doi:10.1021/jm00057a006. PMID 8496936. 



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