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Details Cinnamic acid, 4-hydroxy-, trans-

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Role Reference Substance
nameCinnamic acid, 4-hydroxy-, trans-
MPIMP IDR000198
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
lotS03982-081
purity98
solubility 
general 
amount5
amount unitG
store temperature 1RT
store temperature 2RT
store dryFalse
store under argonFalse
store in darkFalse
contributing authorMeltendorf M, Erban A, 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 out 
date expired 
box number86
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/ReferenceSubstance(guid%27de0c215a-ab8c-4a69-bae2-726998242430%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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