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Details Cinnamic acid, 3-hydroxy-, trans

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Role Reference Substance
nameCinnamic acid, 3-hydroxy-, trans
MPIMP IDR000197
stereoisomerE-
isotopomerambient
formulaC9H8O3
molecular mass164.158
monoisotopic mass164.04735
InChIInChI=1S/C9H8O3/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-6,10H,(H,11,12)/b5-4+
InChIKeyKKSDGJDHHZEWEP-SNAWJCMRSA-N
supplierAldrich
supplier codeH2,300-7
lot35235-041
purity99
solubility 
generalirritant
amount5
amount unitG
store temperature 1RT
store temperature 2RT
store dryFalse
store under argonFalse
store in darkFalse
contributing authorWiggert D, 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 number89
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/ReferenceSubstance(guid%27cadcbe6f-c7dd-47ae-bd16-5a7408376209%27)

Synonyms of Cinnamic acid, 3-hydroxy-, trans

propertyvalue
Beilstein2084229
BRENDA28300
CAS14755-02-3
CAS588-30-7
ChEBI IDChEBI:32357
ChEBI ontologyis a 3-coumaric acid
ChEBI ontologyis conjugate acid of trans-3-coumarate
ChemSpider ID553147
MAPMAN3-Hydroxycinnamate
PubChem CID637541
23 synonym(s)

Metabolites mapped to Cinnamic acid, 3-hydroxy-, trans

Replica of Cinnamic acid, 3-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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