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Details of Cinnamaldehyde, trans-

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Role Metabolite
MPIMP IDM000916
stereoisomer 
isotopomerambient
formulaC9H8O
molecular mass132.160
monoisotopic mass132.05752
InChIInChI=1S/C9H8O/c10-8-4-7-9-5-2-1-3-6-9/h1-8H/b7-4+
InChIKeyKJPRLNWUNMBNBZ-QPJJXVBHSA-N
class 
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/Metabolite(guid%27b99dd6c7-1c6d-4fe3-a172-54bfdb987683%27)

Synonyms of Cinnamaldehyde, trans-

propertyvalue
BRENDA28263
CAS14371-10-9
ChEBI IDChEBI:16731
ChEBI ontologyhas role antifungal drug
ChEBI ontologyhas role flavouring agent
ChEBI ontologyhas role hypoglycemic drug
ChEBI ontologyhas role phenylalanine ammonia-lyase inhibitor
ChEBI ontologyhas role vasodilator agent
ChEBI ontologyis a cinnamaldehydes
ChemSpider ID553117
28 synonym(s)
    of 3    

Derivatives of Cinnamaldehyde, trans-

Reference substances of Cinnamaldehyde, trans-

reference substancesuppliersupplier codelot
Cinnamaldehyde, trans-AldrichC8,068-7 
Cinnamaldehyde, trans-Sigma239968S07483-304
2 reference substance(s)

Isotopomers and stereoisomers of Cinnamaldehyde, trans-

Quantitative Cinnamaldehyde, 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 Cinnamaldehyde, trans- Profile Data

species
no qualitative metabolite profile data available!
compound timestamp information
deposited at 4/9/2009 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 11/26/2013 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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