5-MeO-pyr-T

5-MeO-pyr-T

Names
IUPAC name 5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole
Other names 5-MeO-pyr-T
Identifiers
CAS Number	3949-14-2 N
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL608537 Y
ChemSpider	16153 Y
PubChem CID	17053
CompTox Dashboard (EPA)	DTXSID50192626
InChI InChI=1S/C15H20N2O/c1-18-13-4-5-15-14(10-13)12(11-16-15)6-9-17-7-2-3-8-17/h4-5,10-11,16H,2-3,6-9H2,1H3 Y Key: KAASYKNZNPWPQG-UHFFFAOYSA-N Y InChI=1/C15H20N2O/c1-18-13-4-5-15-14(10-13)12(11-16-15)6-9-17-7-2-3-8-17/h4-5,10-11,16H,2-3,6-9H2,1H3 Key: KAASYKNZNPWPQG-UHFFFAOYAA
SMILES O(c3ccc1c(c(cn1)CCN2CCCC2)c3)C
Properties
Chemical formula	C15H20N2O
Molar mass	244.33 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

5-MeO-pyr-T, or 5-methoxy-N,N-tetramethylenetryptamine, is a lesser-known psychedelic drug. It is the 5-methoxy analog of pyr-T. 5-MeO-pyr-T was first synthesized by Alexander Shulgin. In his book TiHKAL (Tryptamines I Have Known and Loved), neither the dosage nor the duration are known. 5-MeO-pyr-T causes tinnitus, vomiting, and a 5-MeO-DMT-like rushing sensation. At the highest dosage reported in TiHKAL, the subject describes awakening from an apparent fugue state in which they were wandering the streets, with complete amnesia upon awakening of what they had been doing. This suggests that 5-MeO-pyr-T could cause potentially hazardous random behavior at high doses. Very little data exists about the pharmacological properties, metabolism, and toxicity of 5-MeO-pyr-T.

See also

• Pyr-T
• Tryptamine
• Psychedelics, dissociatives and deliriants

External links

• 5-MeO-pyr-T Entry in TIHKAL
• 5-MeO-pyr-T Entry in TiHKAL • info