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N-(2-Cyanoethyl)tryptamine

Pharmaceutical compound From Wikipedia, the free encyclopedia

N-(2-Cyanoethyl)tryptamine (CE-T) is a serotonin receptor modulator and possible psychedelic drug of the tryptamine family related to tryptamine (T).[1][2][3][4] It is the N-(2-cyanoethyl) derivative of tryptamine.[1][2][3][4]

Other namesN-2-Cyanoethyltryptamine; N-Cyanoethyltryptamine; CE-T; CET
ATC code
  • None
Quick facts Clinical data, Other names ...
N-(2-Cyanoethyl)tryptamine
Clinical data
Other namesN-2-Cyanoethyltryptamine; N-Cyanoethyltryptamine; CE-T; CET
Drug classSerotonin receptor agonist; Monoamine releasing agent
ATC code
  • None
Identifiers
  • 3-[2-(1H-indol-3-yl)ethylamino]propanenitrile
CAS Number
PubChem CID
ChemSpider
Chemical and physical data
FormulaC13H15N3
Molar mass213.284 g·mol−1
3D model (JSmol)
  • C1=CC=C2C(=C1)C(=CN2)CCNCCC#N
  • InChI=1S/C13H15N3/c14-7-3-8-15-9-6-11-10-16-13-5-2-1-4-12(11)13/h1-2,4-5,10,15-16H,3,6,8-9H2
  • Key:HGYHTHWLJDVNPB-UHFFFAOYSA-N
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The drug acts as a prodrug of tryptamine and hence is a non-selective serotonin receptor agonist and monoamine releasing agent similarly.[1][2][3][4] It shows greatly sustained tryptamine levels and neurochemical effects in rodents compared to tryptamine itself however.[3][1][4][2] Peak levels of tryptamine with CE-T in the brain were lower than tryptamine itself, whereas total exposure to tryptamine with CE-T in the brain was no different than with tryptamine itself in rodents.[3] CE-T alters brain serotonin and dopamine levels similarly to tryptamine, whereas both drugs have limited effects on brain norepinephrine levels.[3] It produces hypolocomotion in rodents similarly to the combination of tryptamine with a monoamine oxidase inhibitor (MAOI).[4] However, whereas tryptamine was unable to produce hypolocomotion without an MAOI, CE-T showed hypolocomotion regardless of whether the MAOI clorgiline was co-administered.[4]

CE-T was first described in the scientific literature by 1985.[2][3][1][4]

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