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Details of Cinnamic acid, 2-hydroxy-, cis-

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Role Metabolite
MPIMP IDM000585
stereoisomerZ-
isotopomerambient
formulaC9H8O3
molecular mass164.158
monoisotopic mass164.04735
InChIInChI=1S/C9H8O3/c10-8-4-2-1-3-7(8)5-6-9(11)12/h1-6,10H,(H,11,12)/b6-5-
InChIKeyPMOWTIHVNWZYFI-WAYWQWQTSA-N
classAcid (Phenylpropanoic)
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/Metabolite(guid%277af78ce0-7d8b-427a-8189-578c732f4e8e%27)

Synonyms of Cinnamic acid, 2-hydroxy-, cis-

propertyvalue
BRENDA84667
ChEBI IDChEBI:28873
ChEBI ontologyis a 2-coumaric acid
ChEBI ontologyis conjugate acid of cis-2-coumarate
ChemSpider ID4444389
PubChem CID5280841
PubChem SID92297876
synonym(2Z)-3-(2-hydroxyphenyl)acrylic acid
synonym(2Z)-3-(2-hydroxyphenyl)prop-2-enoic acid
synonym2-Coumarinate
16 synonym(s)

Derivatives of Cinnamic acid, 2-hydroxy-, cis-

Reference substances of Cinnamic acid, 2-hydroxy-, cis-

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No Reference substances found!

Isotopomers and stereoisomers of Cinnamic acid, 2-hydroxy-, cis-

Quantitative Cinnamic acid, 2-hydroxy-, cis- 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, 2-hydroxy-, cis- 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 5/21/2012 by Hummel J., Max Planck Institute of Molecular Plant Physiology, Bioinformatics, Am Muehlenberg 1, D-14476 Golm, Germany
modified by users Hummel J.
service last updated 03/01/2017 © 2008-2014 Golm Metabolome Database - All rights reserved
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