INDOPAN

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C11H14N2
Molecular Weight	174.2423
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of INDOPAN

Structure Search

SMILES

CC(N)CC1=CNC2=CC=CC=C12

InChI

InChIKey=QSQQQURBVYWZKJ-UHFFFAOYSA-N

InChI=1S/C11H14N2/c1-8(12)6-9-7-13-11-5-3-2-4-10(9)11/h2-5,7-8,13H,6,12H2,1H3

HIDE SMILES / InChI

Molecular Formula	C11H14N2
Molecular Weight	174.2423
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 08:35:52 UTC 2023` Edited by `admin` on `Sat Dec 16 08:35:52 UTC 2023`
Record UNII	BIK35ACJ0Q
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

INDOPAN

Common Name

English

2-(1H-INDOL-3-YL)-1-METHYLETHYLAMINE

Systematic Name

English

3-(2-AMINOPROPYL)INDOLE

Systematic Name

English

1H-INDOLE-3-ETHANAMINE, .ALPHA.-METHYL-

Systematic Name

English

AMT-

Common Name

English

164 E

Code

English

.ALPHA.-METHYL-.BETA.-INDOLEETHYLAMINE

Common Name

English

INDOLE, 3-(2-AMINOPROPYL)-

Systematic Name

English

(±)-.ALPHA.-METHYLTRYPTAMINE

Systematic Name

English

DL-.ALPHA.-METHYLTRYPTAMINE

Common Name

English

DL-3-(2-AMINOPROPYL)INDOLE

Common Name

English

.ALPHA.-METHYLTRYPTAMINE

Systematic Name

English

U 14

Code

English

3-(2-AMINOPROPYL)-1H-INDOLE

Systematic Name

English

SPIRALS

Common Name

English

NSC-97069

Code

English

.ALPHA.-METHYLTRYPTAMINE [MI]

Common Name

English

AMT

Common Name

English

RO 3-0926

Code

English

.ALPHA.-METHYL-3-INDOLEETHANAMINE

Systematic Name

English

.ALPHA.-METHYLTRYPTAMINE-

Systematic Name

English

.ALPHA.MT

Common Name

English

Classification Tree Code System Code

DEA NO.

7432

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

WIKIPEDIA

TiHKAL

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

WIKIPEDIA

Designer-drugs-.alpha.-Methyltryptamine

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

Code System Code Type Description

EPA CompTox

DTXSID00861850

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

PRIMARY

MERCK INDEX

m7477

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

PRIMARY

Merck Index

DRUG BANK

DB01446

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

PRIMARY

FDA UNII

BIK35ACJ0Q

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

PRIMARY

WIKIPEDIA

alpha-Methyltryptamine

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

PRIMARY

α-Methyltryptamine (abbreviated as αMT, AMT) is a psychedelic, stimulant, and entactogen drug of the tryptamine class. It was originally developed as an antidepressant by workers at Upjohn in the 1960s,[4] and was used briefly as an antidepressant in Russia under the trade name Indopan before being discontinued. αMT has been shown as a reversible inhibitor of the enzyme monoamine oxidase (MAO) in-vitro and in-vivo. In rats the potency of αMT as an MAO-A inhibitor in the brain was approximately equal to that of harmaline at equimolar doses.[note 1] Dexamphetamine did not enhance the 5-hydroxytryptophan-induced rise of serotonin at any level.

NSC

97069

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

PRIMARY

CHEBI

59020

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

PRIMARY

ECHA (EC/EINECS)

206-073-7

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

PRIMARY

PUBCHEM

9287

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

PRIMARY

CAS

299-26-3

Created by admin on Sat Dec 16 08:35:52 UTC 2023 , Edited by admin on Sat Dec 16 08:35:52 UTC 2023

PRIMARY

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