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Details of Melatonin, 6-hydroxy-

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Role	Metabolite
MPIMP ID	M001081
stereoisomer
isotopomer	ambient
formula	C13H16N2O3
molecular mass	248.278
monoisotopic mass	248.11609
InChI	InChI=1S/C13H16N2O3/c1-8(16)14-4-3-9-7-15-11-6-12(17)13(18-2)5-10(9)11/h5-7,15,17H,3-4H2,1-2H3,(H,14,16)
InChIKey	OMYMRCXOJJZYKE-UHFFFAOYSA-N
class
application/atom+xml	http://gmd.mpimp-golm.mpg.de/REST/gmd.svc/Metabolite(guid%270733a77f-d227-41fd-853e-28134cb5ac46%27)

Synonyms of Melatonin, 6-hydroxy-

property	value
BRENDA	30498
CAS	2208-41-5
ChEBI ID	ChEBI:308079
ChemSpider ID	1794
MetaCyc	CPD-12014
PubChem CID	1864
PubChem SID	24278458
PubChem SID	92297621
synonym	3-(N-Acetylaminoethyl)-6-hydroxy-5-methoxyindole
synonym	6-Hydroxymelatonin
12 synonym(s)
Page of 2 Results per page:

Derivatives of Melatonin, 6-hydroxy-

analyte	stereoisomer	isotopomer
Melatonin, 6-hydroxy- (3TMS)		ambient
1 analyte(s)

Reference substances of Melatonin, 6-hydroxy-

reference substance	supplier	supplier code	lot
Melatonin, 6-hydroxy-	Sigma	H0627	082K0991
1 reference substance(s)

Isotopomers and stereoisomers of Melatonin, 6-hydroxy-

metabolite	stereoisomer	isotopomer
no hits!

Quantitative Melatonin, 6-hydroxy- Profile Data

Each graph visualises metabolite concentrations across a single metabolite profiling experiment. Each box plot represents relative (normalised) metabolite concentrations for single replica groups in the specific metabolite profiling experiment.

Name	Organism	Factor	Heatmap	Box plot	Variance	Anova F score
no metabolite profile(s) found.

Qualitative Melatonin, 6-hydroxy- Profile Data

species
no qualitative metabolite profile data available!

compound timestamp information
deposited	at 4/16/2009 by Strehmel N., Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
last changed	at 8/7/2013 by Hummel J., Max Planck Institute of Molecular Plant Physiology, Bioinformatics, Am Muehlenberg 1, D-14476 Golm, Germany
modified by users	Strehmel N., Hummel J.

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