3-MeO-PCP: Difference between revisions
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Dissociative anesthetic that is roughly 10 times stronger than 4-MeO-PCP. May also have opioid or dopaminergic activity. | |||
Dissociative that is roughly 10 times stronger than 4-MeO-PCP. | |||
= History = | |||
3-Methoxyphencyclidine (3-MeO-PCP) is a dissociative anesthetic drug that has been sold online as a research chemical. The compound was first synthesized in 1979 to investigate the structure-activity relationship of phencyclidine derivatives. The activity of 3-MeO-PCP in man was not described until 1999 when a chemist using the pseudonym John Q. Beagle wrote that 3-MeO-PCP was qualitatively similar to PCP with comparable potency. | |||
= Dosage = | = Dosage = | ||
Oral Threshold: 1.5- | Oral Threshold: 1.5-3 mg Light: 3-5mg Common: 5-8mg Strong: 8-12mg Heavy: 12mg+ | ||
= Duration = | = Duration = | ||
Onset: 20-40 minutes. | Oral Onset: 20-40 minutes. | ||
Duration: 3-5 hours +/- 1 hour depending on dose. | |||
Insufflated Onset: 5-15 minutes | |||
Duration for oral and insufflated: 3-5 hours +/- 1 hour depending on dose. | |||
After-effects: 2-48 hours. | After-effects: 2-48 hours. | ||
= Effects = | = Effects = | ||
* Dissociation | |||
* Difficulty walking | |||
* Difficulty talking | |||
* Time dilation | |||
* Music appreciation | |||
* Produces an inner stillness as if all the leaky naggings of the subconscious are completely muted | |||
= Harm Reduction = | |||
Do not drive or operate heavy machinery. Take extra precaution if going out in public on 3-MeO-PCP. Do not drink alcohol or take any other drugs. | |||
= Chemistry and Pharmacology = | = Chemistry and Pharmacology = | ||
3-MeO-PCP binds to the NMDA receptor with higher affinity than PCP and has the highest affinity of the three isomeric anisyl-substitutions, followed by 2-MeO-PCP and 4-MeO-PCP. 3-MeO-PCP has a Ki of 20 nM for the NMDA receptor, 216 nM for the serotonin transporter and 42 for the sigma1 receptor | |||
= Legal = | = Legal = | ||
May be Class B in UK as an analog of MXE. | |||
May be illegal in the US as part of the Analog Act. | |||
= Sites = | |||
[http://www.vice.com/read/interview-with-ketamine-chemist-704-v18n2 Interview with a 3-MeO Chemist] | |||
[http://onlinelibrary.wiley.com/doi/10.1002/dta.1620/abstract From MXE to PCP] | |||
[[Category:Drugs]] | [[Category:Drugs]] | ||
[[Category:Dissociative]] | [[Category:Dissociative]] | ||
Revision as of 13:15, 21 July 2014
Dissociative anesthetic that is roughly 10 times stronger than 4-MeO-PCP. May also have opioid or dopaminergic activity.
History
3-Methoxyphencyclidine (3-MeO-PCP) is a dissociative anesthetic drug that has been sold online as a research chemical. The compound was first synthesized in 1979 to investigate the structure-activity relationship of phencyclidine derivatives. The activity of 3-MeO-PCP in man was not described until 1999 when a chemist using the pseudonym John Q. Beagle wrote that 3-MeO-PCP was qualitatively similar to PCP with comparable potency.
Dosage
Oral Threshold: 1.5-3 mg Light: 3-5mg Common: 5-8mg Strong: 8-12mg Heavy: 12mg+
Duration
Oral Onset: 20-40 minutes.
Insufflated Onset: 5-15 minutes
Duration for oral and insufflated: 3-5 hours +/- 1 hour depending on dose.
After-effects: 2-48 hours.
Effects
- Dissociation
- Difficulty walking
- Difficulty talking
- Time dilation
- Music appreciation
- Produces an inner stillness as if all the leaky naggings of the subconscious are completely muted
Harm Reduction
Do not drive or operate heavy machinery. Take extra precaution if going out in public on 3-MeO-PCP. Do not drink alcohol or take any other drugs.
Chemistry and Pharmacology
3-MeO-PCP binds to the NMDA receptor with higher affinity than PCP and has the highest affinity of the three isomeric anisyl-substitutions, followed by 2-MeO-PCP and 4-MeO-PCP. 3-MeO-PCP has a Ki of 20 nM for the NMDA receptor, 216 nM for the serotonin transporter and 42 for the sigma1 receptor
Legal
May be Class B in UK as an analog of MXE.
May be illegal in the US as part of the Analog Act.