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Cannabinoid

THJ-2201

Also called AM-2201 Indazole

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Common dose · Smoked1–2 mg PW
Onset5–10 minutes PW
Total1–2 hours PW
After-effects60–90 minutes PW

Dosage

Smoked

SourceThresholdLightCommonStrongHeavy
PsychonautWiki< 0.5 mg PW0.5–1 mg PW1–2 mg PW2–5 mg PW5 mg+ PW
What dose are you on? (self-reported, unverified)
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Duration

Route · sourceOnsetCome-upPeakOffsetTotalAfter-effects
Smoked · PsychonautWiki5–10 minutes PW–30–45 minutes PW0–0 minutes (Abrupt) PW1–2 hours PW60–90 minutes PW

Mixing

Acute combinations: what happens when these are taken close together. Entries backed by a medical journal or agency are listed first.

Backed by medical journals

Awaiting sourcePeer-reviewed reports on acute combinations, from PubMed and the journals the harm reduction sites cite.

PsychonautWiki also lists dangerous combinations shared across a whole group (cannabis) in a table this page does not copy. Read that list on PsychonautWiki.

Risks and toxicity

The toxicity and long-term health effects of recreational THJ-2201 use do not seem to have been studied in any scientific context and the exact toxic dosage is unknown. This is because THJ-2201 has very little history of human usage. Anecdotal evidence from people who have tried THJ-2201 within the community suggest that there do not seem to be any negative health effects attributed to simply trying this drug at low to moderate doses by itself and using it sparingly (but nothing can be completely guaranteed). PW

Informal experiments have shown that overdose will cause physical discomfort including heart palpitations, vertigo and sedation at much lower than dangerous doses, usually causing the user to suffer moderate to severe anxiety or fall asleep. PW

It has often been recommended that those with severe pre-existing mental conditions should not ingest these substances due to the way they strongly increase one's current state of mind and emotions. Also, like THC, prolonged usage of synthetic cannabinoids may increase one's disposition to mental illness and psychosis, particularly in vulnerable individuals with risk factors for psychotic illnesses (like a past or family history of schizophrenia).[6–9] PW

As synthetic cannabinoids are active in the milligram range (with below 5mg being a common dose), it is important to use proper precautions when dosing to avoid a negative experience. PW

It is strongly recommended that one use harm reduction practices when using this drug. PW

Tolerance and addiction potential

As with other synthetic cannibanoids, the chronic use of THJ-2201 can be considered moderately addictive with a high potential for abuse and is capable of causing psychological dependence among certain users. When addiction has developed, cravings and withdrawal effects may occur if a person suddenly stops their usage. PW

Tolerance to many of the effects of THJ-2201 develops with prolonged and repeated use. This results in users having to administer increasingly large doses to achieve the same effects. After that, it takes about 3 - 7 days for the tolerance to be reduced to half and 1 - 2 weeks to be back at baseline (in the absence of further consumption). THJ-2201 presents cross-tolerance with all cannabinoids, meaning that after the consumption of THJ-2201 all cannabinoids will have a reduced effect. PW

Testing

Awaiting sourceReagent reactions and test kit guidance from a harm reduction testing service.

Effects

Awaiting sourceSubjective and physical effects from PsychonautWiki or TripSit.

Overview

THJ-2201 (1-​[(5-​fluoropentyl)-​1H-​indazol-​3-​yl](naphthalen-​1-​yl)methanone) is a synthetic cannabinoid and analog of AM-2201. It has been marketed by many research chemical vendors as a legal alternative to the popular AM-2201, which had been banned in 2011. PW

THJ-2201 is an indazole-based synthetic cannabinoid that presumably acts as a potent agonist of the CB₁ receptor and has been sold online as a designer drug.[1–4] WP

It is a structural analog of AM-2201 in which the central indole ring has been replaced by indazole.[5] WP

History

Awaiting sourceHistory and culture from Wikipedia or PsychonautWiki, with their citations.

Pharmacology

Pharmacology

THJ-2201 acts as a full agonist with a binding affinity of 1.34 nM at CB₁ and 1.32 nM at CB₂ cannabinoid receptors.[20] WP

Chemistry

Formula
C23H21FN2O PC
CAS number
1801552-01-1 PC
Molar mass (g/mol)
360.4 PC
IUPAC name (computed by PubChem)
[1-(5-fluoropentyl)indazol-3-yl]-naphthalen-1-ylmethanone PC
SMILES
C1=CC=C2C(=C1)C=CC=C2C(=O)C3=NN(C4=CC=CC=C43)CCCCCF PC
InChIKey
DULWRYKFTVFPTL-UHFFFAOYSA-N PC
PubChem CID
91864533

User reports

Erowid erowid.org

Listings
Awaiting sourceExperience Vault listing and report categories.
Top stories
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Bluelight bluelight.org

Listings
Awaiting sourceTrip report threads and this substance's discussion forum.
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Pop culture

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References

  1. Journal / agency Diao X, Wohlfarth A, Pang S, Scheidweiler KB, Huestis MA. High-Resolution Mass Spectrometry for Characterizing the Metabolism of Synthetic Cannabinoid THJ-018 and Its 5-Fluoro Analog THJ-2201 after Incubation in Human Hepatocytes. Clinical Chemistry. January 2016. doi:10.1373/clinchem.2015.243535 · PMID 26430074
  2. Journal / agency Shevyrin V, Melkozerov V, Nevero A, Eltsov O, Morzherin Y, Shafran Y. 3-Naphthoylindazoles and 2-naphthoylbenzoimidazoles as novel chemical groups of synthetic cannabinoids: chemical structure elucidation, analytical characteristics and identification of the first representatives in smoke mixtures. Forensic Science International. September 2014. doi:10.1016/j.forsciint.2014.06.022 · PMID 25036783
  3. Journal / agency Uchiyama N, Shimokawa Y, Kawamura M, Kikura-Hanajiri R, Hakamatsuka T. Chemical analysis of a benzofuran derivative, 2-(2-ethylaminopropyl)benzofuran (2-EAPB), eight synthetic cannabinoids, five cathinone derivatives, and five other designer drugs newly detected in illegal products. Forensic Toxicology. August 2014. doi:10.1007/s11419-014-0238-5
  4. Journal / agency Diao X, Scheidweiler KB, Wohlfarth A, Zhu M, Pang S, Huestis MA. Strategies to distinguish new synthetic cannabinoid FUBIMINA (BIM-2201) intake from its isomer THJ-2201: metabolism of FUBIMINA in human hepatocytes. Forensic Toxicology. 2016. doi:10.1007/s11419-016-0312-2 · PMID 27547265 · PMC4971051
  5. Other THJ-2201
  6. Journal / agency Arseneault, L., Cannon, M., Witton, J., Murray, R. M. Causal association between cannabis and psychosis: examination of the evidence. The British Journal of Psychiatry. February 2004. doi:10.1192/bjp.184.2.110
  7. Journal / agency Every-Palmer, S. Synthetic cannabinoid JWH-018 and psychosis: An explorative study. Drug and Alcohol Dependence. September 2011. doi:10.1016/j.drugalcdep.2011.01.012
  8. Journal / agency Schneir, A. B., Cullen, J., Ly, B. T. “Spice” Girls: Synthetic Cannabinoid Intoxication. The Journal of Emergency Medicine. 1 March 2011. doi:10.1016/j.jemermed.2010.10.014
  9. Journal / agency Vearrier, D., Osterhoudt, K. C. A Teenager With Agitation: Higher Than She Should Have Climbed. Pediatric Emergency Care. June 2010. doi:10.1097/PEC.0b013e3181e4f416
  10. Other Bekendtgørelse om euforiserende stoffer - ni nye stoffer tilføjet
  11. Other Anlage II BtMG
  12. Other Achtundzwanzigste Verordnung zur Änderung betäubungsmittelrechtlicher Vorschriften
  13. Other § 29 BtMG
  14. Other Zaudējis spēku - Noteikumi par Latvijā kontrolējamajām narkotiskajām vielām, psihotropajām vielām un prekursoriem
  15. Other http://www.folkhalsomyndigheten.se/nyheter-och-press/nyhetsarkiv/2014/november/cannabinoider-foreslas-bli-klassade-som-halsofarlig-vara/
  16. Other Verordnung des EDI über die Verzeichnisse der Betäubungsmittel, psychotropen Stoffe, Vorläuferstoffe und Hilfschemikalien
  17. Other The Misuse of Drugs Act 1971 (Amendment) Order 2016
  18. Journal / agency Schedules of controlled substances: temporary placement of three synthetic cannabinoids into schedule I. Final order. PMID 25730924
  19. Other Gesetz über den Verkehr mit Betäubungsmitteln (Betäubungsmittelgesetz - BtMG) Anlage II (zu § 1 Abs. 1) (verkehrsfähige, aber nicht verschreibungsfähige Betäubungsmittel)
  20. Journal / agency Hess C, Schoeder CT, Pillaiyar T, Madea B, Müller CE. Pharmacological evaluation of synthetic cannabinoids identified as constituents of spice. Forensic Toxicology. 1 July 2016. doi:10.1007/s11419-016-0320-2 · PMID 27429655 · PMC4929166

Text and values on this page are quoted from PsychonautWiki (CC BY-SA 4.0), Wikipedia (CC BY-SA 4.0), PubChem (public domain). Each value links to the exact revision it came from.