Buy Desmetramadol O-desmethyltramadol (O-DSMT)
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Desmetramadol (INNTooltip International Nonproprietary Name), also known as O-desmethyltramadol (O-DSMT), is an opioid analgesic and the main active metabolite of tramadol.[2] Tramadol is demethylated by the liver enzyme CYP2D6[3] to desmetramadol in the same way as codeine, and so similarly to the variation in effects seen with codeine, individuals who have a less active form of CYP2D6 will tend to have reduced analgesic effects from tramadol. Because desmetramadol itself does not need to be metabolized to induce an analgesic effect, it can be used in individuals with CYP2D6 inactivating mutations.
Desmetramadol is commonly encountered as a designer drug online[4] in powder form or as an ingredient in pressed pills due to being unscheduled in many jurisdictions. Outside of its role as a metabolite, a chemical used in research, and as a recreational drug, desmetramadol has a very limited history of human usage and is not approved for medicinal use in any country as of 2025.
Pharmacology
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Pharmacodynamics
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(+)-Desmetramadol is a G-protein biased μ-opioid receptor full agonist.[5] It shows comparatively far lower affinity for the δ- and κ-opioid receptors.[6] The two enantiomers of desmetramadol show quite distinct pharmacological profiles;[7] both (+) and (−)-desmetramadol are inactive as serotonin reuptake inhibitors,[8] but (−)-desmetramadol retains activity as a norepinephrine reuptake inhibitor,[9] and so the mix of both the parent compound and metabolites contributes significantly to the complex pharmacological profile of tramadol. While the multiple receptor targets can be beneficial in the treatment of pain (especially complex pain syndromes such as neuropathic pain), they increase the potential for drug interactions compared to other opioids, and may also contribute to side effects. Desmetramadol is also an antagonist of the serotonin 5-HT2C receptor, at pharmacologically relevant concentrations, via competitive inhibition.[10] This suggests that the apparent anti-depressant properties of tramadol may be at least partially mediated by desmetramadol, thus prolonging the duration of therapeutic benefit. Inhibition of the 5-HT2C receptor is a suggested factor in the mechanism of anti-depressant effects of agomelatine and maprotiline. The potential selectivity and favorable side effect profile of desmetramadol compared to tramadol, makes it more suitable for use as antidepressant, although clinical development appears to have stopped. Upon inhibition of the receptor, downstream signaling causes dopamine and norepinephrine release, and the receptor is thought to significantly regulate mood, anxiety, feeding, and reproductive behavior. 5-HT2C receptors regulate dopamine release in the striatum, prefrontal cortex, nucleus accumbens, hippocampus, hypothalamus, and amygdala, among others.[11] Research indicates that some suicide victims have an abnormally high number of 5-HT2C receptors in the prefrontal cortex.[12] There is some mixed evidence that agomelatine, a 5-HT2C antagonist, is an effective antidepressant.[13] Antagonism of 5-HT2C receptors by agomelatine results in an increase of dopamine and norepinephrine activity in the frontal cortex.
Pharmacokinetics
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
Buy Desmetramadol O-desmethyltramadol (O-DSMT)
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O-Desmethyltramadol (O-DSMT) is an opioid that has primarily been used indirectly due to it being a primary metabolite of the analgesic tramadol. It has other names such as O-Desmethyltramadol, Desmetramadol, O-DSMT, Omnitram, has a strong similarity in action on Furanyl-Fentanyl. is a synthetic opipodic drug, an active metabolite of tramadol of the cyclohexanol class. O-DSMT IUPAC: 3- (2 – ((dimethylamino) methyl) -1-hydroxycyclohexyl) phenol. o-dsmt has a similar molecular structure to tramadol.Firstly O-DSMT has good analgesic properties, acts as a sedative, euphoric, but can quickly become addictive. It has the most potent effect compared to tramadol. Buy O-DSMT online
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O-DMST, has efficacy in the same conditions as typical opioids like oxycodone and morphine. Also, based on research with tramadol, there’s some evidence indicating how much benefit people receive from tramadol is at least partly dependent on how much O-DSMT they produce (Kirchheiner, 2008; Stamer, 2007; Poulsen, 1996). Buy O-DSMT online
Metabolites
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Desmetramadol is metabolized in the liver into the active metabolite N,O-didesmethyltramadol via CYP3A4 and CYP2B6. The inactive tramadol metabolite N-desmethyltramadol is metabolized into the active metabolite N,O-didesmethyltramadol by CYP2D6
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O-DSMT, also known as O-Desmethyltramadol, is a synthetic opioid compound derived from tramadol. It exhibits analgesic properties and is often used in laboratory settings for research purposes. O-DSMT interacts with opioid receptors in the central nervous system, producing effects similar to other opioids.
Key Features and Characteristics of odsmt
- Pain Relief: This product is a potent analgesic that can provide relief from moderate to severe pain. It exerts its analgesic effects by binding to the mu-opioid receptors in the central nervous system, thereby reducing the perception of pain.
- Opioid Activity: This product exhibits opioid-like activity due to its structural similarity to tramadol. It acts as a mu-opioid receptor agonist, which results in pain relief, sedation, and euphoria.
- Metabolism: This product is a metabolite of tramadol. Tramadol is metabolized in the liver by the enzyme CYP2D6 to form O-DSMT. This metabolite has a longer half-life than tramadol, leading to prolonged effects.
- Research Chemical: This product is frequently used as a research chemical. Researchers study its pharmacological properties, potential therapeutic applications, and its effects on opioid receptors and pain pathways.
- Dosage: The suggested dosage of this product is 1mg. However, it is crucial to note that dosages should be determined by researchers based on their specific experimental requirements and in compliance with legal and ethical guidelines.
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Molecular Formula: C15H23NO2
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CAS: 80456-81-1
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Molecular Weight: 249.354 g·mol−1
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Buy O-DSMT online. O-Desmethyltramadol (O-DSMT) is an opioid that has primarily been used indirectly due to it being a primary metabolite of the analgesic tramadol.
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O-DSMT is a high-affinity ligand that can be used to treat opioid dependence. It’s similar to the – and -opioid receptors. Both O-DSMT and its metabolites are active reuptake inhibitors.
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