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4-HO-MPMI

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
4-HO-MPMI
Clinical data
Other names4-Hydroxy-N-methyl-(α,N-trimethylene)tryptamine; Lucigenol
ATC code
  • None
Legal status
Legal status
Identifiers
  • (R)-3-(N-methylpyrrolidin-2-ylmethyl)-4-hydoxyindole
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H17N2O
Molar mass229.303 g·mol−1
3D model (JSmol)
  • OC1=C2C(C[C@@]3([H])CCCN3C)=CNC2=CC=C1
  • InChI=1S/C14H18N2O/c1-16-7-3-4-11(16)8-10-9-15-12-5-2-6-13(17)14(10)12/h2,5-6,9,11,15,17H,3-4,7-8H2,1H3/t11-/m1/s1 ☒N
  • Key:XYRKPZYRLSWABB-LLVKDONJSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

4-HO-MPMI, also known as4-hydroxy-N-methyl-(α,N-trimethylene)tryptamine or aslucigenol, is apsychedelic drug of thepyrrolidinylmethylindole andcyclized tryptamine families.[1]

Interactions

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See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Pharmacology

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Pharmacodynamics

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Theaffinity (Ki) of 4-HO-MPMI for theserotonin5-HT2A receptor has been found to be 13 nM.[1] It producespsychedelic-appropriate responding inanimal tests with similarpotency asDOI.[1] The drug has twoenantiomers, with only the (R)-enantiomer being active.[1]

Chemistry

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Analogues

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Analogues of 4-HO-MPMI includeMPMI,5-MeO-MPMI,5F-MPMI,CP-135,807,4-HO-McPeT,4-HO-pyr-T, andSN-22, among others.

History

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4-HO-MPMI was developed by the team led byDavid E. Nichols fromPurdue University in the late 1990s.[1]

See also

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References

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  1. ^abcdeGerasimov 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.CiteSeerX 10.1.1.690.4941.doi:10.1021/jm990325u.PMID 10514296.

External links

[edit]
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
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Cyclized
Bioisosteres
Phenethylamines
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5-HT1
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5-HT2A
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5-HT2C
5-HT37
5-HT3
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5-HT5A
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Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
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Isotryptamines
Related compounds
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