VANILLYLAMINE

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NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C8H11NO2
Molecular Weight	153.1784
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of VANILLYLAMINE

SMILES

COC1=CC(CN)=CC=C1O

InChI

InChIKey=WRPWWVNUCXQDQV-UHFFFAOYSA-N

InChI=1S/C8H11NO2/c1-11-8-4-6(5-9)2-3-7(8)10/h2-4,10H,5,9H2,1H3

HIDE SMILES / InChI

Approval Year

PubMed

Show entries

Title	Date	PubMed
Methyl jasmonate modulated biotransformation of phenylpropanoids to vanillin related metabolites using Capsicum frutescens root cultures.	2005 Feb	15820659
The Pun1 gene for pungency in pepper encodes a putative acyltransferase.	2005 Jun	15918882
Enzymatic synthesis of capsaicin analogs and their effect on the T-type Ca2+ channels.	2007 May 4	17362879
In vitro hepatic and skin metabolism of capsaicin.	2008 Apr	18180272
Functional loss of pAMT results in biosynthesis of capsinoids, capsaicinoid analogs, in Capsicum annuum cv. CH-19 Sweet.	2009 Sep	19473323

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Patents

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Name

Type

Language

VANILLYLAMINE

Systematic Name

English

CAPSIVIROL-T

Brand Name

English

(3-METHOXY-4-HYDROXYPHENYL)METHYLAMINE

Systematic Name

English

4-HYDROXY-3-METHOXYBENZYLAMINE

Systematic Name

English

4-(AMINOMETHYL)-2-METHOXYPHENOL

Systematic Name

English

Showing 1 to 5 of 12 entries

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Code System

Code

Type

Description

DAILYMED

1WEZ91E3Z0

PRIMARY

CAS

1196-92-5

PRIMARY

CHEBI

149596

PRIMARY

WIKIPEDIA

Vanillylamine

PRIMARY

RXCUI

156075

PRIMARY

RxNorm

Showing 1 to 5 of 10 entries

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ACTIVE MOIETY


					1WEZ91E3Z0

PARENT (METABOLITE)


					S07O44R1ZM

CAPSAICIN

SALT/SOLVATE (PARENT)


					YD97FX0LRF

VANILLYLAMINE HYDROCHLORIDE