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Details of Piperidine-2-carboxylic acid

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Role Metabolite
MPIMP IDM000528
stereoisomer(S)-
isotopomerambient
formulaC6H11NO2
molecular mass129.157
monoisotopic mass129.07898
InChIInChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m0/s1
InChIKeyHXEACLLIILLPRG-YFKPBYRVSA-N
classAcid (N-heterocycle)
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/Metabolite(guid%277c6a2ded-5e15-4dfb-bf48-f9d231169779%27)

Synonyms of Piperidine-2-carboxylic acid

propertyvalue
Beilstein81093
BRENDA59615
CAS3105-95-1
ChEBI IDChEBI:30913
ChEBI ontologyis a pipecolic acid
ChEBI ontologyis conjugate base of L-pipecolate
ChEBI ontologyis enantiomer of D-pipecolic acid
ChEBI ontologyis tautomer of L-pipecolic acid zwitterion
ChemSpider ID388365
MetaCycL-PIPECOLATE
22 synonym(s)

Derivatives of Piperidine-2-carboxylic acid

Reference substances of Piperidine-2-carboxylic acid

reference substancesuppliersupplier codelot
Piperidine-2-carboxylic acidSigma806151094978
Piperidine-2-carboxylic acidSigma-Aldrich P2519MKBK3901V
2 reference substance(s)

Isotopomers and stereoisomers of Piperidine-2-carboxylic acid

Quantitative Piperidine-2-carboxylic acid Profile Data

Each graph visualises metabolite concentrations across a single metabolite profiling experiment. Each box plot represents relative (normalised) metabolite concentrations for single replica groups in the specific metabolite profiling experiment.

Qualitative Piperidine-2-carboxylic acid Profile Data

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 6/19/2014 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., Fehrle I., Kopka J.
service last updated 04/12/2020 © 2008-2014 Golm Metabolome Database - All rights reserved
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