Summary
Alpha-PCyP is a stimulant substance classified within the cathinone class and marketed online as a designer drug. Within a group of alpha-substituted pyrrolidinyl cathinone derivatives created in 2015, the alpha-cyclopentyl variation was identified to possess roughly equivalent in vitro potency as an inhibitor of the dopamine transporter compared to the alpha-propyl derivative α-PVP. Conversely, the alpha-cyclohexyl variation α-PCyP exhibited approximately twice the power.
| Identifiers | |
|---|---|
| IUPAC name | |
| CAS Number | 1803168-11-7 |
|---|---|
| PubChem CID | 155884437 |
| UNII | PJ2S9WH4A2 |
| Chemical and physical data | |
| Formula | C18H25NO |
| Molar mass | 271.404 g·mol−1 |
Legal status
| Legal status | |
|---|---|
| Legal status | CA: Schedule I DE: NpSG (Industrial and scientific use only) UK: Under Psychoactive Substances Act US: Unscheduled Illegal in Virginia |
FAQ
1. What is α-PCYP?
- α-PCYP is a synthetic compound categorized within the cathinone class. It is known for its stimulant properties and is often sold online as a designer drug.
2. What are the effects of α-PCYP?
- α-PCYP is recognized for its stimulating effects, including increased alertness, energy, and euphoria. Users may also experience heightened sociability.
3. Is α-PCYP legal?
- The legal status of α-PCYP can vary by country and region. In some areas, it may be classified as a controlled substance, making its manufacture, possession, or distribution illegal without proper authorization. It’s essential to check local regulations to determine its legal status.
4. What are the health risks associated with α-PCYP use?
- Using α-PCYP can carry various health risks, such as an increased heart rate, anxiety, paranoia, and potential addiction. Long-term effects are not well understood due to limited research.
5. Can α-PCYP be detected in drug tests?
- α-PCYP may potentially be detectable in drug tests, especially in urine screenings. However, its inclusion in standard drug tests may vary. Specialized tests may be required for accurate detection.
6. Are there any street names for α-PCYP?
- Street names for α-PCYP may vary by region and include nicknames or slang terms used in the illicit drug trade.
7. Is α-PCYP used for any medical purposes?
- α-PCYP is not approved for any medical use and is primarily encountered as a recreational or illicit substance.
8. What should I do if I suspect someone is using α-PCYP?
- If you suspect someone is using α-PCYP or any other illicit substance, it’s crucial to encourage them to seek professional help. Substance abuse can have severe health and social consequences, and early intervention is essential.
9. Where can I get more information about α-PCYP and its risks?
- For comprehensive information about α-PCYP, associated risks, and harm reduction strategies, consider consulting local substance abuse resources, addiction treatment centers, or medical professionals specializing in addiction and mental health. Additionally, government health agencies often provide information on substance abuse and its consequences.
References
- “§ 54.1-3446. Classification in Schedule I.” Virginia State Law. Retrieved on September 14, 2023.
- Kolanos R, Sakloth F, Jain AD, Partilla JS, Baumann MH, Glennon RA (October 2015). “Altering the Structure of the Designer Stimulant α-Pyrrolidinovalerophenone (α-PVP) Affects Its Potency at Dopamine Transporters.” Published in ACS Chemical Neuroscience. Volume 6, Issue 10, Pages 1726–1731. DOI: 10.1021/acschemneuro.5b00160. PMC 5349767. PMID 26217965.
- Glennon RA, Dukat M (2016). “Investigating the Relationship Between Structure and Activity of Synthetic Cathinones.” Published in Current Topics in Behavioral Neurosciences. Volume 32, Pages 19–47. DOI: 10.1007/7854_2016_41. ISBN 978-3-319-52442-9. PMC 5818155. PMID 27830576.
- Baumann MH, Walters HM, Niello M, Sitte HH (2018). “Neuropharmacology of Synthetic Cathinones.” Published in New Psychoactive Substances. Handbook of Experimental Pharmacology. Volume 252, Pages 113–142. DOI: 10.1007/164_2018_178. ISBN 978-3-030-10560-0. PMC 7257813. PMID 30406443.