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Details of Quinoline-2-carboxylic acid, 4,8-dihydroxy-

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Role Metabolite
MPIMP IDM001063
stereoisomer 
isotopomerambient
formulaC10H7NO4
molecular mass205.167
monoisotopic mass205.03751
InChIInChI=1S/C10H7NO4/c12-7-3-1-2-5-8(13)4-6(10(14)15)11-9(5)7/h1-4,12H,(H,11,13)(H,14,15)
InChIKeyFBZONXHGGPHHIY-UHFFFAOYSA-N
class 
application/atom+xmlhttp://gmd.mpimp-golm.mpg.de/REST/gmd.svc/Metabolite(guid%27b5ff212d-76cb-4875-8a36-c67d8e69489c%27)

Synonyms of Quinoline-2-carboxylic acid, 4,8-dihydroxy-

propertyvalue
BRENDA1941
CAS59-00-7
ChEBI IDChEBI:217069
ChemSpider ID5497
PubChem CID5699
PubChem SID24893378
PubChem SID92298434
synonym4,8-Dihydroxyquinaldic acid
synonym4,8-Dihydroxyquinoline-2-carboxylic acid
synonym4,8-Dihydroxy-quinoline-2-carboxylic acid(Xanthurenate)
11 synonym(s)

Derivatives of Quinoline-2-carboxylic acid, 4,8-dihydroxy-

Reference substances of Quinoline-2-carboxylic acid, 4,8-dihydroxy-

Isotopomers and stereoisomers of Quinoline-2-carboxylic acid, 4,8-dihydroxy-

Quantitative Quinoline-2-carboxylic acid, 4,8-dihydroxy- 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.
NameOrganismFactorHeatmapBox plotVarianceAnova F score
no metabolite profile(s) found.

Qualitative Quinoline-2-carboxylic acid, 4,8-dihydroxy- Profile Data

species
no qualitative metabolite profile data available!
compound timestamp information
deposited at 4/16/2009 by Strehmel N., Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
last changed at 5/21/2012 by Hummel J., Max Planck Institute of Molecular Plant Physiology, Bioinformatics, Am Muehlenberg 1, D-14476 Golm, Germany
modified by users Strehmel N., Hummel J.
service last updated 17/02/2017 © 2008-2014 Golm Metabolome Database - All rights reserved
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