CHEBI:47952 - D-glucopyranuronic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name D-glucopyranuronic acid
ChEBI ID CHEBI:47952
ChEBI ASCII Name D-glucopyranuronic acid
Definition A D-glucuronic acid in cyclic pyranose form.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C6H10O7
Net Charge 0
Average Mass 194.13940
Monoisotopic Mass 194.04265
InChI InChI=1S/C6H10O7/c7-1-2(8)4(5(10)11)13-6(12)3(1)9/h1-4,6-9,12H,(H,10,11)/t1-,2-,3+,4-,6?/m0/s1
InChIKey AEMOLEFTQBMNLQ-AQKNRBDQSA-N
SMILES OC1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O
Metabolite of Species Details
Chlamydomonas reinhardtii (NCBI:txid3055) See: PubMed
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): algal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via glucuronic acid )
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
(via glucuronic acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-glucopyranuronic acid (CHEBI:47952) has role algal metabolite (CHEBI:84735)
D-glucopyranuronic acid (CHEBI:47952) is a D-glucuronic acid (CHEBI:4178)
D-glucopyranuronic acid (CHEBI:47952) is conjugate acid of D-glucopyranuronate (CHEBI:58720)
D-glucopyranuronic acid (CHEBI:47952) is enantiomer of L-glucopyranuronic acid (CHEBI:79049)
Incoming β-D-Xylp-(1→2)-D-GlcpA (CHEBI:151701) has functional parent D-glucopyranuronic acid (CHEBI:47952)
1-O-(α-D-glucopyranuronosyl)-N-tetradecanoyldihydrosphingosine (CHEBI:60476) has functional parent D-glucopyranuronic acid (CHEBI:47952)
4-O-methyl-α-D-glucuronoside ester (CHEBI:171667) has functional parent D-glucopyranuronic acid (CHEBI:47952)
[4)-β-D-GlcpA-(1→4)-α-D-GlcpNAc-(1→]n (CHEBI:62819) has functional parent D-glucopyranuronic acid (CHEBI:47952)
[4)-β-D-GlcpA-(1→4)-α-D-GlcpNAc6OS-(1→]n (CHEBI:62820) has functional parent D-glucopyranuronic acid (CHEBI:47952)
[4)-β-D-GlcpA-(1→4)-α-D-GlcpNS6OS-(1→]n (CHEBI:62821) has functional parent D-glucopyranuronic acid (CHEBI:47952)
glycosylglucopyranuronic acid (CHEBI:152563) has functional parent D-glucopyranuronic acid (CHEBI:47952)
heparosan D-glucuronic acid (CHEBI:85801) has functional parent D-glucopyranuronic acid (CHEBI:47952)
UDP-D-glucuronic acid (CHEBI:197331) has functional parent D-glucopyranuronic acid (CHEBI:47952)
α-D-glucuronic acid (CHEBI:42717) is a D-glucopyranuronic acid (CHEBI:47952)
β-D-glucuronic acid (CHEBI:28860) is a D-glucopyranuronic acid (CHEBI:47952)
heparosan-N-sulfate D-glucuronic acid (CHEBI:17831) is a D-glucopyranuronic acid (CHEBI:47952)
D-glucopyranuronate (CHEBI:58720) is conjugate base of D-glucopyranuronic acid (CHEBI:47952)
L-glucopyranuronic acid (CHEBI:79049) is enantiomer of D-glucopyranuronic acid (CHEBI:47952)
IUPAC Name
D-glucopyranuronic acid
Synonyms Sources
Glucuronate KEGG COMPOUND
Glucuronic acid KEGG COMPOUND
Manual Xrefs Databases
C00001123 KNApSAcK
C00191 KEGG COMPOUND
D-Glucopyranuronate MetaCyc
DB03156 DrugBank
ECMDB04073 ECMDB
HMDB0000127 HMDB
View more database links
Registry Numbers Types Sources
1427741 Reaxys Registry Number Reaxys
397418 Gmelin Registry Number Gmelin
528-16-5 CAS Registry Number ChemIDplus
6556-12-3 CAS Registry Number KEGG COMPOUND
Citations Waiting for Citations Types Sources
1276 PubMed citation Europe PMC
16658890 PubMed citation Europe PMC
17440709 PubMed citation Europe PMC
19093370 PubMed citation Europe PMC
6814425 PubMed citation Europe PMC
6838587 PubMed citation Europe PMC
7504304 PubMed citation Europe PMC
7540499 PubMed citation Europe PMC
8049386 PubMed citation Europe PMC
8111290 PubMed citation Europe PMC
Last Modified
25 September 2023