结构:CCC(N)Cc1c[nH]c2ccccc12
HCID8367

Alpha-Ethyltryptamine

1-(1H-indol-3-yl)butan-2-amine

C12H16N2188.27 g/molCAS 2235-90-7

IDENTITY

结构与身份

标准 SMILES
CCC(N)Cc1c[nH]c2ccccc12
InChIKey
ZXUMUPVQYAFTLF-UHFFFAOYSA-N
分子式
C12H16N2
平均分子量
188.27 g/mol
单同位素质量
188.13134852

COMPUTED

结构计算性质

已同步
XLogP
2.5
极性表面积
41.8 Ų
氢键供体
2
氢键受体
1
可旋转键
3
重原子
14
形式电荷
0
复杂度
181

PROPERTIES

实验与物化性质

来源:PubChem
LogS

-2.57

Solubility

510

Melting Point

221

Kovats Retention Index

1848

HAZARDS

危害信息

来源:PubChem
Regulatory Information

DEA schedule I controlled substance

REGULATORY

法规信息

来源:PubChem
Regulatory Information

DEA schedule I controlled substance

PHARMACOLOGY

药理信息

来源:PubChem
Pharmacodynamics

αET is a stimulant and psychedelic with MDMA like physiological effects. Like MDMA, increases in locomotor activity and mood elevation can be seen post administration. [2]

Mechanism of Action

The mechanism of action responsible for its antidepressant activity was believed to lie in its ability to inhibit monoamine oxidase, while its stimulant activity on the central nervous system appeared to result from its structural similarity to indole-based psychedelics. [5] Research discovered αET to be both a monoamine oxidase inhibitor and a potent monoamine releasing agent capable of serotonergic neurotoxicity. [3] The ability to release serotonin was linked to αET's MDMA like properties. [2] αET has been shown to release serotonin pre-synaptically, as well as lesser amounts of norepinephrine and dopamine.

ALIASES

名称与别名

80
ETRYPTAMINEalpha-Ethyltryptamine3-(2-Aminobutyl)indole2235-90-73-IndolylbutylamineEtriptaminaMonaseRo 3-1932Etryptaminum1H-Indole-3-ethanamine, alpha-ethyl-alphaETDTXSID1046764NSC-88061GR181O3R32DTXCID9026764NSC880612-ethyltryptamine3-(2-aminobutylindole)RefChem:1393041-(1H-indol-3-yl)butan-2-amine

REACTIONS

参与反应

4