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Details of Cinnamic acid, 3-hydroxy-, trans

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Role Metabolite
MPIMP IDM000214
stereoisomerE-
isotopomerambient
formulaC9H8O3
molecular mass164.158
monoisotopic mass164.04735
InChIInChI=1S/C9H8O3/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-6,10H,(H,11,12)/b5-4+
InChIKeyKKSDGJDHHZEWEP-SNAWJCMRSA-N
classAcid (Phenylpropanoic)
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/Metabolite(guid%27358818fd-674f-4656-96af-40f17c30f2ee%27)

Synonyms of Cinnamic acid, 3-hydroxy-, trans

propertyvalue
Beilstein2084229
BRENDA28300
CAS14755-02-3
CAS588-30-7
ChEBI IDChEBI:32357
ChEBI ontologyis a 3-coumaric acid
ChEBI ontologyis conjugate acid of trans-3-coumarate
ChemSpider ID553147
MAPMAN3-Hydroxycinnamate
PubChem CID637541
23 synonym(s)

Derivatives of Cinnamic acid, 3-hydroxy-, trans

Reference substances of Cinnamic acid, 3-hydroxy-, trans

Isotopomers and stereoisomers of Cinnamic acid, 3-hydroxy-, trans

Quantitative Cinnamic acid, 3-hydroxy-, trans 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.
NameOrganismFactorHeatmapBox plotVarianceAnova F score
no metabolite profile(s) found.

Qualitative Cinnamic acid, 3-hydroxy-, trans Profile Data

species
no qualitative metabolite profile data available!
compound timestamp information
deposited at 8/29/2006 by Hummel J., Max Planck Institute of Molecular Plant Physiology, Bioinformatics, Am Muehlenberg 1, D-14476 Golm, Germany
last changed at 8/16/2012 by Kopka J., Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
modified by users Hummel J., Kopka J.
service last updated 17/02/2017 © 2008-2014 Golm Metabolome Database - All rights reserved
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