kyanite
Bluelighter
- Joined
- Oct 15, 2005
- Messages
- 248
The drug I'm describing here is Tramadol without the methyl on the phenolic group(-OH instead of -OCH3). A lot of people on Bluelight have tried Tramadol, I haven't, but from what I've read it feels as if it's missing something. Not to mention Tramadol also acts on other systems than the opiate receptors(GABA, adrenergic, serotonin).
Theres a file on the net showing the results of a drug dependance study by Virginia Commonwealth University, and one of the drugs was this O-desmethyl-tramadol(called NIH 10913). It suppresses morphine withdrawals with a morphine like potency in monkeys. Pretty good for a pretty simple compound.
But the question is if Tramadol and this O-desmethyl have a similar relationship like Codeine and Morphine. Roughly 10% of codeine is turned into morphine, O-desmethyl is roughly morphine's potency, and Tramadol is 10% potency morphine given IV/IM. Maybe the opiate effects of tramadol is actually from the O-desmethyl.
Is there any other information on o-desmethyl tramadol? If it doesn't have the adrenergic and serotonin effects of tramadol, then tramadol might be more useful than we think.
edit: from wikipedia
Metabolism
Tramadol undergoes hepatic metabolism via the cytochrome P450 isozyme CYP2D6, being O- and N-demethylated to 5 different metabolites. Of these, M1 is the most significant since it has 200 times the μ-affinity of (+)-tramadol, and furthermore has an elimination half-life of 9 hours compared to 6 hours for tramadol itself. In the 6% of the population who have slow CYP2D6 activity, there is therefore a slightly reduced analgesic effect. Phase II hepatic metabolism renders the metabolites water-soluble and they are renally excreted. Thus reduced doses may be used in renal and hepatic impairment.
Okay, M1 is the o-desmethyl-tramadol, so apparently it's pretty potent... any more info?
Theres a file on the net showing the results of a drug dependance study by Virginia Commonwealth University, and one of the drugs was this O-desmethyl-tramadol(called NIH 10913). It suppresses morphine withdrawals with a morphine like potency in monkeys. Pretty good for a pretty simple compound.
But the question is if Tramadol and this O-desmethyl have a similar relationship like Codeine and Morphine. Roughly 10% of codeine is turned into morphine, O-desmethyl is roughly morphine's potency, and Tramadol is 10% potency morphine given IV/IM. Maybe the opiate effects of tramadol is actually from the O-desmethyl.
Is there any other information on o-desmethyl tramadol? If it doesn't have the adrenergic and serotonin effects of tramadol, then tramadol might be more useful than we think.

edit: from wikipedia
Metabolism
Tramadol undergoes hepatic metabolism via the cytochrome P450 isozyme CYP2D6, being O- and N-demethylated to 5 different metabolites. Of these, M1 is the most significant since it has 200 times the μ-affinity of (+)-tramadol, and furthermore has an elimination half-life of 9 hours compared to 6 hours for tramadol itself. In the 6% of the population who have slow CYP2D6 activity, there is therefore a slightly reduced analgesic effect. Phase II hepatic metabolism renders the metabolites water-soluble and they are renally excreted. Thus reduced doses may be used in renal and hepatic impairment.
Okay, M1 is the o-desmethyl-tramadol, so apparently it's pretty potent... any more info?
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