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|WikiProject Psychedelics, Dissociatives and Deliriants|
Should dextrorphan be classified an opioid, with Ki's ranging from 420 to >1,000 nM? Or is this only formaly because of the "pseudomorphinan" skeleton?--22.214.171.124 18:07, 4 November 2007 (UTC)
- OK, it should:) Pethidine has even lower affinities. Sorry for the monologue.--126.96.36.199 18:09, 4 November 2007 (UTC)
Space Filling Model
So I noticed that the space filling model is wrong in one spot: http://en.wikipedia.org/wiki/Image:Dextrorphan_3d.gif
At the top where the oxygen (red) comes off of one of the benzene ring carbons (grey). The model shows both a hydrogen (white) AND oxygen atom on the same carbon, there should be no hydrogen on that carbon.
Inconsistent Molecular Structure Orientation
I'm not good with graphics or I would correct this. It's not so much a problem, but the molcular structures for DXO and DXM are oriented completely differently from one and another. This makes it very difficult for someone to see the structural similarities/differences. It would be nice if they could be oriented the same way. --Jmcclare (talk) 20:44, 3 January 2009 (UTC)
Additionally, it would be nice if the structures were oriented similarly to morphine for likewise reasons. The DXO molecule is already oriented like the morphine molecule. --Jmcclare (talk) 23:31, 3 January 2009 (UTC)
I removed the following, which I'd tagged with "citation needed" because I think that it should have a citation.
"Dextrorphan's opioid, serotonin, and norepinephrine reuptake-inhibiting effects are pharmacologically insignificant."