DOPF
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IUPAC name
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Chemical and physical data | |
Formula | C14H22FNO2 |
Molar mass | 255.333 g·mol−1 |
3D model (JSmol) | |
SMILES
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InChI
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DOPF is a designer drug from the substituted amphetamine family. It was first synthesised by Alexander Shulgin and David Nichols in 1989 but was never published at the time, and was finally disclosed in Daniel Trachsel's review of the field in 2013. It has a binding affinity (Ki) of 9 nM at the serotonin receptor 5-HT2A but is not known to have been tested in humans.[1]
See also
References
- ↑ Trachsel D, Lehmann D, Enzensperger C (2013). Phenethylamine Von der Struktur zur Funktion [Phenethylamine From structure to function] (in German). Nachtschatten Verlag AG. p. 778-780. ISBN 978-3-03788-700-4.
Phenethylamines |
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Amphetamines |
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Phentermines |
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Cathinones |
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Phenylisobutylamines | |
Phenylalkylpyrrolidines | |
Catecholamines (and close relatives) |
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Miscellaneous |
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Psychedelics (5-HT2A agonists) |
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Dissociatives (NMDAR antagonists) |
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Deliriants (mAChR antagonists) |
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Others |
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