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7-Chloro-AMT
| Column 1 |
|---|
| IUPAC name |
| 1-(7-chloro-1H-indol-3-yl)propan-2-amine |
| .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}711-99-9 Y |
| 13900 |
| 13298 |
| J4Y6BPR38T |
| C11H13ClN2 |
| 208.69 g·mol−1 |
| Interactive image |
| SMILES |
| CC(CC1=CNC2=C1C=CC=C2Cl)N |
| InChI |
| InChI=1S/C11H13ClN2/c1-7(13)5-8-6-14-11-9(8)3-2-4-10(11)12/h2-4,6-7,14H,5,13H2,1H3Key:OHEYTFPYHFDAJQ-UHFFFAOYSA-N |
7-Chloro-α-methyltryptamine (7-Cl-AMT) is a tryptamine derivative with stimulant effects, invented in the 1960s. It is a weak monoamine oxidase inhibitor but its pharmacology has not otherwise been studied by modern techniques, though several closely related compounds are known to act as serotonin–dopamine releasing agents and agonists of the 5-HT2A receptor.
- Substituted tryptamine
- 7-Chlorotryptamine
- 5-Chloro-AMT
- 5-Chloro-DMT
- 5-Fluoro-AMT
- 5-Fluoro-AET
- 5-Fluoro-DMT
- 6-Fluoro-AMT
- 7-Methyl-DMT
- 7-Methyl-AET
- 7F-5-MeO-MET
- O-4310
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