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MPMI (drug)

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
MPMI
Clinical data
Other names3-(N-Methylpyrrolidin-3-ylmethyl)indole;N-Methyl-α,N-trimethylenetryptamine; α,N-Trimethylene-N-methyltryptamine
Drug classSerotonin receptor agonist
Identifiers
  • 3-[(1-methylpyrrolidin-2-yl)methyl]-1H-indole
CAS Number
PubChemCID
ChemSpider
Chemical and physical data
FormulaC14H18N2
Molar mass214.312 g·mol−1
3D model (JSmol)
  • CN1CCCC1CC2=CNC3=CC=CC=C32
  • InChI=1S/C14H18N2/c1-16-8-4-5-12(16)9-11-10-15-14-7-3-2-6-13(11)14/h2-3,6-7,10,12,15H,4-5,8-9H2,1H3
  • Key:HCTCDEAMCNSARD-UHFFFAOYSA-N

MPMI, also known as3-(N-methylpyrrolidin-3-ylmethyl)indole or asN-methyl-α,N-trimethylenetryptamine, is apyrrolidinylmethylindole andcyclized tryptamine which acts as aserotonin receptor agonist. It has been studied as an analogue and trace impurity of theantimigraine drugeletriptan but is otherwise little known.[1][2]

Chemistry

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Analogues

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Analogues of MPMI include4-HO-MPMI,5-MeO-MPMI,5F-MPMI,eletriptan,CP-122288,CP-135807,10,11-secoergoline (α,N-Pip-T),pyr-T,SN-22, andα,N,N-trimethyltryptamine, among others.

See also

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References

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  1. ^FI 105812, Wythes MJ, Macor JE, "Menetelmä terapeuttisesti käyttökelpoisten indolijohdannaisten valmistamiseksi", issued 14 April 1993, assigned to Pfizer, Inc. 
  2. ^US 5607951, Macor JE, Wythes MJ, "Indole derivatives", issued 4 March 1997, assigned to Pfizer, Inc. 

External links

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Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
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Cyclized
Lysergamides
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5-HT1
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5-HT1E
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5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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