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Details Cinnamic acid, 4-hydroxy-, trans-

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Role Reference Substance
nameCinnamic acid, 4-hydroxy-, trans-
MPIMP IDR100165
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
supplierAldrich
supplier codeH2,320-1
lot 
purity 
solubility 
general 
amount 
amount unit 
store temperature 1 
store temperature 2 
store dryFalse
store under argonFalse
store in darkFalse
contributing authorKopka J, Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Kopka J), Am Muehlenberg 1, D-14476 Golm, Germany
date of order 
date in2004-08-26
date out2005-09-01
date expired 
box number 
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/ReferenceSubstance(guid%2718ba724f-5c07-4970-a97e-be8460439c12%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)

Metabolites mapped to Cinnamic acid, 4-hydroxy-, trans-

Replica of Cinnamic acid, 4-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 6/8/2015 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.
service last updated 17/02/2017 © 2008-2014 Golm Metabolome Database - All rights reserved
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