Ericjones03
Bluelighter
- Joined
- Apr 3, 2018
- Messages
- 38
Hey there guys, I'm planning on venturing into the world of research chem opioids- namely O-DSMT or O-Desmethyltramadol but I've got a problem that's probably shared by many others too. Please correct me if I simply haven't looked enough, but the problem is that I feel as though there's a huge lack of information on dosages (PW has a page for it, but I always look for multiple sources), experiences, and general information for O-DSMT. I've only seen small threads consisting of a few posts here and there, but no megathread for it, and considering how it's said to show more of the traditional opiate high (it was even compared to Morphine in one post) vs. Tramadol's stack of stimulation and opiate euphoria, it seems as though it would be educational to have a place for all to discuss this chemical. To start, if anyone has detailed experience reports- yes, I know about Erowid, but there's only 7 so far- please share then here, I'm very interested in giving this a try, as Tramadol is one of my favorite DOC's. And for all other information that anybody has, it'd be great to hear about that too, too much research can never harmful, but too little sure as hell can!
Thanks everyone!
KK edit:
O-desmethyltramadol is the main active metabolite (metabolized by CYP2D6) of the pharmaceutical tramadol.
What we know:
The half life of O-DSMT seems to be around 9 hours [1]
O-DSMT seems to not be a SSRI (tested concentrations up to 5 µmol/l) [2]
(-)-O-DSMT seems to be a NRI [3] while (+)-O-DSMT might cause norepinephrine release [3][4]
O-DSMT seems to inhibit the serotonin receptor 5-HT2C [5]
(+)-O-DSMT has a Ki (in µM) of 0.017 for mu-opioid receptor (for reference morphine has a Ki of 0.0021), 0.69 for delta and 1.8 for kappa [6]
Thanks everyone!
KK edit:
O-desmethyltramadol is the main active metabolite (metabolized by CYP2D6) of the pharmaceutical tramadol.
What we know:
The half life of O-DSMT seems to be around 9 hours [1]
O-DSMT seems to not be a SSRI (tested concentrations up to 5 µmol/l) [2]
(-)-O-DSMT seems to be a NRI [3] while (+)-O-DSMT might cause norepinephrine release [3][4]
O-DSMT seems to inhibit the serotonin receptor 5-HT2C [5]
(+)-O-DSMT has a Ki (in µM) of 0.017 for mu-opioid receptor (for reference morphine has a Ki of 0.0021), 0.69 for delta and 1.8 for kappa [6]
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