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Details Cinnamic acid, 2-hydroxy-, trans-

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Role Reference Substance
nameCinnamic acid, 2-hydroxy-, trans-
MPIMP IDR000614
stereoisomerE-
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-AATRIKPKSA-N
supplierSigma
supplier codeC4400
lot20K3727
purity 
solubility 
general 
amount5
amount unitG
store temperature 1RT
store temperature 2RT
store dryFalse
store under argonFalse
store in darkFalse
contributing authorEckardt A, Boelling C, Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
date of order 
date in2000-01-01
date out 
date expired 
box number47
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/ReferenceSubstance(guid%27c9ce0e95-f578-411c-92f5-339aae234e90%27)

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

propertyvalue
BRENDA28310
CAS614-60-8
ChEBI IDChEBI:18125
ChEBI ontologyis a 2-coumaric acid
ChEBI ontologyis conjugate acid of trans-2-coumarate
ChemSpider ID553146
MAPMAN2-Coumarate
PubChem CID637540
PubChem SID92298030
synonym(2E)-3-(2-hydroxyphenyl)-2-propenoic acid
27 synonym(s)

Metabolites mapped to Cinnamic acid, 2-hydroxy-, trans-

Replica of Cinnamic acid, 2-hydroxy-, trans-

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.
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