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

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Role Metabolite
MPIMP IDM000117
stereoisomerE-
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-ZZXKWVIFSA-N
classAcid (Phenylpropanoic)
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/Metabolite(guid%270c1bff2d-2cf7-4fc1-9f76-3268c2c7f783%27)

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

propertyvalue
BRENDA28301
CAS501-98-4
CAS7400-08-0
ChEBI IDChEBI:32374
ChEBI ontologyis a 4-coumaric acid
ChEBI ontologyis conjugate acid of trans-4-coumarate
ChemSpider ID553148
MAPMAN4-Coumarate
PubChem CID637542
PubChem SID24893127
30 synonym(s)
    of 3    

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

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

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

Quantitative Cinnamic acid, 4-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.

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

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 9/25/2018 by Fehrle I., 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., Fehrle I.
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