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Details Cinnamic acid, 2-hydroxy-, trans-

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Role Reference Substance
nameCinnamic acid, 2-hydroxy-, trans-
MPIMP IDR002151
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
supplierSSX
supplier code6029
lot 
purity 
solubility 
general 
amount 
amount unit 
store temperature 1 
store temperature 2 
store dry 
store under argon 
store in dark 
contributing authorTohge, RIKEN Plant Service Center, Metabolome Analysis Research Team, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, JAPAN
date of order 
date in 
date out 
date expired 
box number 
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/ReferenceSubstance(guid%27ea578dd0-df57-494a-b51f-c9b4b8513369%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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