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1 See also  





2 References  














Pyr-T






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From Wikipedia, the free encyclopedia
 


Pyr-T

Names

Preferred IUPAC name

3-[2-(Pyrrolidin-1-yl)ethyl]-1H-indole

Other names

N,N-Tetramethylenetryptamine

Identifiers

CAS Number

3D model (JSmol)

ChemSpider

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C14H18N2/c1-2-6-14-13(5-1)12(11-15-14)7-10-16-8-3-4-9-16/h1-2,5-6,11,15H,3-4,7-10H2 checkY

    Key: CVTZCBLFHNGYDQ-UHFFFAOYSA-N checkY

  • InChI=1/C14H18N2/c1-2-6-14-13(5-1)12(11-15-14)7-10-16-8-3-4-9-16/h1-2,5-6,11,15H,3-4,7-10H2

    Key: CVTZCBLFHNGYDQ-UHFFFAOYAE

    • c2c(c1ccccc1[nH]2)CCN3CCCC3

    Properties

    Chemical formula

    C14H18N2

    Molar mass

    214.312 g·mol−1

    Melting point

    193 to 194 °C (379 to 381 °F; 466 to 467 K) (HCl salt.)

    Boiling point

    170 to 180 °C (338 to 356 °F; 443 to 453 K) (Freebase at 0.05mm/Hg.)

    log P

    2.74410

    Vapor pressure

    1.02x10−5mmHg

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Pyr-T (N,N-tetramethylenetryptamine) is a lesser-known, possible psychedelic drug. Pyr-T was first characterized by S. Mitzal.[1] Toxicity testing was later performed by Hunt and Brimblecombe, and although a lethal dosage was found in rats, a value is not given.[2] In the book TiHKAL (Tryptamines I Have Known and Loved), neither the dosage nor the duration are reported.[3][4]

    Pyr-T produces few to no effects in humans, but some behavioral changes were observed in animal tests.[2] Very little data exists about the pharmacological properties, metabolism, and toxicity of pyr-T.

    See also[edit]

    References[edit]

    1. ^ Mitzal, S. (1962). "N/A". Dissertationes Pharm. 14: 305.
  • ^ a b Hunt, R. R.; Brimblecombe, R. W. (July 1967). "Synthesis and Biological Activity of Some Ring-Substituted Tryptamines". Journal of Medicinal Chemistry. 10 (4): 646–648. doi:10.1021/jm00316a027. PMID 4962512.
  • ^ Shulgin, Alexander; Shulgin, Ann (1997). TiHKAL, The Continuation (1st ed.). Berkeley, CA, USA: Transform Press. pp. 577–578. ISBN 0-9630096-9-9. Retrieved 7 April 2018.
  • ^ Krasowski MD, Ekins S. Using cheminformatics to predict cross reactivity of “designer drugs” to their currently available immunoassays. J Cheminform 6, 22 (2014). doi:10.1186/1758-2946-6-22
  • 2,alpha-DMT
  • 2-Me-DET
  • 2-Methyl-5-HT
  • 2,N,N-TMT
  • 4,5-DHP-DMT
  • 4,5-MDO-DMT
  • 4,5-MDO-DiPT
  • 4-AcO-DALT
  • 4-AcO-DET
  • 4-AcO-DMT
  • 4-AcO-DiPT
  • 4-AcO-EPT
  • 4-AcO-NMT
  • 4-AcO-MALT
  • 4-AcO-MET
  • 4-AcO-DPT
  • 4-AcO-MiPT
  • 4-F-5-MeO-DMT
  • 4-HO-5-MeO-DMT
  • 4-HO-DALT
  • 4-HO-DBT
  • 4-HO-DET
  • 4-HO-DiPT
  • 4-HO-DPT
  • 4-HO-DSBT
  • 4-HO-EPT
  • 4-HO-MALT
  • 4-HO-MET
  • 4-HO-McPT
  • 4-HO-McPeT
  • 4-HO-MiPT
  • 4-HO-MPMI
  • 4-HO-MPT
  • 4-HO-MsBT
  • 4-HO-NMT
  • 4-HO-PiPT
  • 4-HO-pyr-T
  • 4-HO-αMT
  • 4-Me-αET
  • 4-Me-αMT
  • 4-MeO-DiPT
  • 4-MeO-DMT
  • 4-MeO-MiPT
  • 4-PrO-DMT
  • 5,6-MeO-MiPT
  • 5,6-MDO-DiPT
  • 5,6-MDO-DMT
  • 5,6-MDO-MiPT
  • 5,7-Dihydroxytryptamine
  • 5-BT
  • 5-Bromo-DMT
  • 5-CT
  • 5-Chloro-αMT
  • 5-Chloro-DMT
  • 5-Ethoxy-αMT
  • 5-Ethoxy-DMT
  • 5-Ethyl-DMT
  • 5-Fluoro-AET
  • 5-Fluoro-αMT
  • 5-Fluoro-DET
  • 5-Fluoro-DMT
  • 5-Fluoro-EPT
  • 5-Fluoro-MET
  • 5-HO-αMT
  • 5-HO-DiPT
  • 5-HTP
  • 5-iPrO-AMT
  • 5-MeS-DMT
  • 5-Methoxytryptamine
  • 5-MeO-7,N,N-TMT
  • 5-Methyl-αET
  • 5-MeO-2-TMT
  • 5-MeO-αET
  • 5-MeO-αMT
  • 5-MeO-DALT
  • 5-MeO-DBT
  • 5-MeO-DET
  • 5-MeO-DiPT
  • 5-MeO-DMT
  • 5-MeO-DPT
  • 5-MeO-EiPT
  • 5-MeO-EPT
  • 5-MeO-MALT
  • 5-MeO-MET
  • 5-MeO-MiPT
  • 5-MeO-MPMI
  • 5-MeO-NMT
  • 5-MeO-pyr-T
  • 5-MeO-NBpBrT
  • 5-Methyl-DMT
  • 5-(Nonyloxy)tryptamine
  • 6-Fluoro-αMT
  • 6-Fluoro-DMT
  • 6-Hydroxymelatonin
  • 6-MeO-THH
  • 7-Chloro-AMT
  • 7-Methyl-α-ethyltryptamine
  • 7-Methyl-DMT
  • Acetryptine
  • Aeruginascin
  • αET
  • Alpha,N-DMT
  • α,N,N-Trimethyltryptamine
  • Alpha,N,O-TMS
  • AL-37350A
  • αMT
  • Baeocystin
  • BNC-210
  • Bufotenidine
  • Bufotenin (5-HO-DMT)
  • BW-723C86
  • Convolutindole A
  • CP-132,484
  • DALT
  • DBT
  • Desformylflustrabromine
  • DET
  • DiPT
  • DPT
  • E-6801
  • E-6837
  • Ethocybin
  • EiPT
  • EMDT
  • EPT
  • FGIN-127
  • FGIN-143
  • Harmaline
  • HIOC
  • Ibogaine
  • Idalopirdine
  • Indorenate
  • Iprocin
  • Lespedamine
  • Luzindole
  • MET
  • Methylbutyltryptamine
  • MiPT
  • MPT
  • Miprocin
  • Melatonin
  • MPMI
  • MS-245
  • NAS
  • N-Ethyltryptamine
  • N-Feruloylserotonin
  • NMT
  • DMT
  • Norbaeocystin
  • Normelatonin
  • N-t-Butyltryptamine
  • O-4310
  • Oxypertine
  • Plakohypaphorine
  • PiPT
  • Psilocin (4-HO-DMT)
  • Psilocybin (4-PO-DMT)
  • Pyr-T
  • Rizatriptan
  • RU-28306
  • Serotonin
  • ST-1936
  • Sumatriptan
  • Tryptamine
  • Tryptophan
  • Yohimbine
  • Yuremamine
  • Zolmitriptan

  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Pyr-T&oldid=1170123981"

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    This page was last edited on 13 August 2023, at 08:42 (UTC).

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