From Surf Wiki (app.surf) — the open knowledge base
2C-CPe
| Column 1 |
|---|
| 2C-CPE; 4-Cyclopentyl-2,5-dimethoxyphenethylamine; 2,5-Dimethoxy-4-cyclopentylphenethylamine |
| IUPAC name |
| 2-(4-cyclopentyl-2,5-dimethoxyphenyl)ethanamine |
| .mw-parser-output .plainlist ol,.mw-parser-output .plainlist ul{line-height:inherit;list-style:none;margin:0;padding:0}.mw-parser-output .plainlist ol li,.mw-parser-output .plainlist ul li{margin-bottom:0}169149436 |
| C15H23NO2 |
| 249.354 g·mol−1 |
| Interactive image |
| SMILES |
| COC1=CC(=C(C=C1CCN)OC)C2CCCC2 |
| InChI |
| InChI=1S/C15H23NO2/c1-17-14-10-13(11-5-3-4-6-11)15(18-2)9-12(14)7-8-16/h9-11H,3-8,16H2,1-2H3Key:GIYHLPFOZWFVHO-UHFFFAOYSA-N |
2C-CPe, also known as 4-cyclopentyl-2,5-dimethoxyphenethylamine, is a designer drug from the substituted phenethylamine family, which was first synthesised by Josh Hartsel and colleagues in 2024. It is a moderately potent agonist at the serotonin receptor 5-HT2A in vitro, with a binding affinity (Ki) of 134 nM, slightly weaker than the related cyclopropyl compound 2C-CP. It is not known to have been tested in humans or animals. It is a controlled substance in Canada under phenethylamine blanket-ban language.
-
2C (psychedelics)
-
2C-P
-
2C-Bu
-
2C-iBu
-
2C-CPe - Isomer Design
Ask Mako anything about 2C-CPe — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report