5-Methoxy-7,N,N-trimethyltryptamine

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5-Methoxy-7,N,N-trimethyltryptamine
5-MeO-7-TMT.png
Systematic (IUPAC) name
2-(5-Methoxy-7-methyl-1H-indol-3-yl)-N,N-dimethylethanamine
Identifiers
CAS Number 61018-77-7 N freebase
74798-76-8 oxalate salt
PubChem CID: 12338919
ChemSpider 10578304 YesY
ChEMBL CHEMBL20243 YesY
Chemical data
Formula C14H20N2O
Molecular mass 232.32 g/mol
  • CC1=C(NC=C2CCN(C)C)C2=CC(OC)=C1
  • InChI=1S/C14H20N2O/c1-10-7-12(17-4)8-13-11(5-6-16(2)3)9-15-14(10)13/h7-9,15H,5-6H2,1-4H3 YesY
  • Key:YGAOMGVUIWNFMD-UHFFFAOYSA-N YesY
 NYesY (what is this?)  (verify)

5-Methoxy-7,N,N-trimethyltryptamine (5-MeO-7,N,N-TMT, 5-MeO-7-TMT), is a tryptamine derivative which acts as an agonist at the 5-HT2 serotonin receptors.[1][2] In animal tests, both 7,N,N-TMT and 5-MeO-7,N,N-TMT produced behavioural responses similar to those of psychedelic drugs such as DMT and 5-MeO-DMT, but compounds with larger 7-position substituents such as 7-ethyl-DMT and 7-bromo-DMT did not produce psychedelic-appropriate responding despite high 5-HT2 receptor binding affinity, suggesting these may be antagonists or weak partial agonists for the 5-HT2 receptors.[3] The related compound 7-MeO-MiPT (cf. 5-MeO-MiPT) was also found to be inactive, suggesting that the 7-position has poor tolerance for bulky groups at this position, at least if agonist activity is desired.[4]

See also

References

  1. Benington F, Morin RD, Bradley RJ. 7-(N,N-Trimethyl)-5-methoxytryptamine. Journal of Heterocyclic Chemistry 1976; 13(4):749-751. doi:10.1002/jhet.5570130412
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