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Details of Cinnamic acid, 4-hydroxy-, cis-

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Role Metabolite
MPIMP IDM000587
stereoisomerZ-
isotopomerambient
formulaC9H8O3
molecular mass164.158
monoisotopic mass164.04735
InChIInChI=1S/C9H8O3/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6,10H,(H,11,12)/b6-3-
InChIKeyNGSWKAQJJWESNS-UTCJRWHESA-N
classAcid (Phenylpropanoic)
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/Metabolite(guid%2715f90638-dcf1-4922-afb2-baf5ea308c8c%27)

Synonyms of Cinnamic acid, 4-hydroxy-, cis-

propertyvalue
BRENDA28303
ChEBI IDChEBI:17450
ChEBI ontologyis a 4-coumaric acid
ChEBI ontologyis conjugate acid of cis-4-coumarate
ChemSpider ID1266072
PubChem CID1549106
PubChem SID92298378
synonym(2Z)-3-(4-hydroxyphenyl)acrylic acid
synonym(2Z)-3-(4-hydroxyphenyl)prop-2-enoic acid
synonym(Z)-3-(4-hydroxyphenyl)-2-propenoic acid
21 synonym(s)

Derivatives of Cinnamic acid, 4-hydroxy-, cis-

Reference substances of Cinnamic acid, 4-hydroxy-, cis-

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No Reference substances found!

Isotopomers and stereoisomers of Cinnamic acid, 4-hydroxy-, cis-

Quantitative Cinnamic acid, 4-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.

Qualitative Cinnamic acid, 4-hydroxy-, cis- Profile Data

species
Lotus Japonicus.Gifu
this metabolite was recorded in 1 species
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 17/02/2017 © 2008-2014 Golm Metabolome Database - All rights reserved
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