MiPT
| Clinical data | |
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| Other names | MiPT; N-Methyl-N-isopropyltryptamine |
| Routes of administration | Oral |
| Drug class | Serotonin receptor modulator; Serotonin 5-HT2A receptor agonist; Serotonergic psychedelic; Hallucinogen |
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| Pharmacokinetic data | |
| Onset of action | Oral: 30 minutes Insufflation: <1 minute |
| Duration of action | 3–4 hours |
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| Chemical and physical data | |
| Formula | C14H20N2 |
| Molar mass | 216.328 g·mol−1 |
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Methylisopropyltryptamine (MiPT), also known as N-methyl-N-isopropyltryptamine, is a psychedelic drug of the tryptamine family related to other psychedelics like dimethyltryptamine (DMT) and diisopropyltryptamine (DiPT). It is taken orally.
The drug acts as a serotonin receptor modulator, including as an agonist of the serotonin 5-HT2A receptor. Derivatives of MiPT include 4-HO-MiPT (miprocin) and 5-MeO-MiPT (moxy).
MiPT was first described by David Repke and colleagues in 1981. It was subsequently evaluated and described in Alexander Shulgin's 1997 book TiHKAL (Tryptamines I Have Known and Loved). MiPT was encountered as a novel designer drug by 2005.