6-Methoxytryptamine

COC1=CC2=C(C=C1)C(CCN)=CN2

InChIKey=VOCGEKMEZOPDFP-UHFFFAOYSA-N

InChI=1S/C11H14N2O/c1-14-9-2-3-10-8(4-5-12)7-13-11(10)6-9/h2-3,6-7,13H,4-5,12H2,1H3

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Tandem intramolecular photocycloaddition-retro-Mannich fragmentation as a route to spiro[pyrrolidine-3,3'-oxindoles]. Total synthesis of (+/-)-coerulescine, (+/-)-horsfiline, (+/-)-elacomine, and (+/-)-6-deoxyelacomine.	2010-06-04	20429523
Screening for endogenous substrates reveals that CYP2D6 is a 5-methoxyindolethylamine O-demethylase.	2003-06	12777961

Substance Class	Chemical Created by `admin` on `Tue Apr 01 19:44:10 GMT 2025` Edited by `admin` on `Tue Apr 01 19:44:10 GMT 2025`
Record UNII	83E56U9G2L
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

6-Methoxytryptamine

Common Name

English

2-(2-Aminoethyl)-5-methoxyindole

Preferred Name

English

1H-Indole-3-ethanamine, 6-methoxy-

Systematic Name

English

6-Methoxy-1H-indole-3-ethanamine

Systematic Name

English

Code System Code Type Description

FDA UNII

83E56U9G2L