Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C12H16N2 |
| Molecular Weight | 188.2688 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(N)CC1=CNC2=CC=CC=C12
InChI
InChIKey=ZXUMUPVQYAFTLF-UHFFFAOYSA-N
InChI=1S/C12H16N2/c1-2-10(13)7-9-8-14-12-6-4-3-5-11(9)12/h3-6,8,10,14H,2,7,13H2,1H3
Approval Year
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| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
TiHKAL
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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DEA NO. |
7249
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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WIKIPEDIA |
Designer-drugs-Monase
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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NCI_THESAURUS |
C667
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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| Code System | Code | Type | Description | ||
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1117
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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DB01546
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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100000082116
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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SUB07347MIG
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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CHEMBL1619758
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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1276
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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PRIMARY | |||
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alpha-Ethyltryptamine
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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PRIMARY | α-Ethyltryptamine (αET, AET), also known as etryptamine (INN, BAN, USAN), is a psychedelic, stimulant, and entactogenic drug of the tryptamine class. It was originally developed and marketed as an antidepressant under the brand name Monase by Upjohn in the 1960s. αET is structurally and pharmacologically related to αMT, α-methyltryptamine, and it is believed[4] its central stimulant activity is probably not due to its activity as an MAOI, but appears to stem from its structural relationship to the indolic psychedelics. In contrast to αMT, αET is less stimulating and hallucinogenic, its effects resembling more those of entactogens like MDMA ("Ecstasy"). | ||
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C72772
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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m727
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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PRIMARY | Merck Index | ||
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C038034
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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2235-90-7
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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GR181O3R32
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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8367
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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DTXSID1046764
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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PRIMARY | |||
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PE 006
Created by
admin on Fri Dec 15 16:17:30 UTC 2023 , Edited by admin on Fri Dec 15 16:17:30 UTC 2023
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PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)
SALT/SOLVATE (PARENT)
