5-MeO-MPMI
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Systematic (IUPAC) name | |
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(R)-3-(N-methylpyrrolidin-2-ylmethyl)-5-methoxyindole | |
Identifiers | |
CAS Number |
143321-57-7 ![]() |
PubChem | CID 9881324 |
ChemSpider |
8057000 ![]() |
ChEMBL |
CHEMBL137485 ![]() |
Chemical data | |
Formula | C15H19N2O |
Molar mass | 243.323 g/mol |
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5-MeO-MPMI (also known as 5-Methoxy-N-methyl-(α,N-trimethylene)tryptamine) is a tryptamine derivative that is a psychedelic drug. It was first developed by the team led by JE Macor in 1992,[1] and subsequently investigated by the team led by David Nichols from Purdue University in the late 1990s. This compound produces psychedelic-appropriate responding in animal tests with a similar potency to the amphetamine-derived psychedelic DOI, and has two enantiomers, with only the (R)-enantiomer being active.[2]
See also
References
- ↑ Macor JE, Blake J, Fox CB, Johnson C, Koe BK, Lebel LA, Morrone JM, Ryan K, Schmidt AW, Schulz DW; et al. (1992). "Synthesis and serotonergic pharmacology of the enantiomers of 3-[(N-methylpyrrolidin-2-yl)methyl]-5-methoxy-1H-indole: discovery of stereogenic differentiation in the aminoethyl side chain of the neurotransmitter serotonin". Journal of Medicinal Chemistry 35 (23): 4503–4305. doi:10.1021/jm00101a032. PMID 1447752.
- ↑ Gerasimov M, Marona-Lewicka D, Kurrasch-Orbaugh DM, Qandil AM, Nichols DE (1999). "Further studies on oxygenated tryptamines with LSD-like activity incorporating a chiral pyrrolidine moiety into the side chain". Journal of Medicinal Chemistry 42 (20): 4257–4263. doi:10.1021/jm990325u. PMID 10514296.
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