CHEBI:40583 - α-D-GalpA-(1→4)-α-D-GalpA

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name α-D-GalpA-(1→4)-α-D-GalpA
ChEBI ID CHEBI:40583
ChEBI ASCII Name alpha-D-GalpA-(1->4)-alpha-D-GalpA
Definition A α-D-GalpA-(1→4)-D-GalpA in which the anomeric hydroxy group has α- configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:40577, CHEBI:22369
Supplier Information
Download Molfile XML SDF
Formula C12H18O13
Net Charge 0
Average Mass 370.26352
Monoisotopic Mass 370.07474
InChI InChI=1S/C12H18O13/c13-1-2(14)7(9(18)19)25-12(5(1)17)24-6-3(15)4(16)11(22)23-8(6)10(20)21/h1-8,11-17,22H,(H,18,19)(H,20,21)/t1-,2+,3+,4+,5+,6+,7-,8-,11-,12-/m0/s1
InChIKey IGSYEZFZPOZFNC-MMGXBETBSA-N
SMILES O[C@H]1O[C@@H]([C@H](O[C@H]2O[C@@H]([C@H](O)[C@H](O)[C@H]2O)C(O)=O)[C@H](O)[C@H]1O)C(O)=O
Metabolite of Species Details
Clostridium cellulovorans (NCBI:txid1493) 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): bacterial xenobiotic metabolite
Any bacterial metabolite produced by metabolism of a xenobiotic compound in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing α-D-GalpA-(1→4)-α-D-GalpA (CHEBI:40583) has role bacterial xenobiotic metabolite (CHEBI:76976)
α-D-GalpA-(1→4)-α-D-GalpA (CHEBI:40583) is a α-D-GalpA-(1→4)-D-GalpA (CHEBI:141006)
α-D-GalpA-(1→4)-α-D-GalpA (CHEBI:40583) is conjugate acid of α-D-GalpA-(1→4)-α-D-GalpA(2−) (CHEBI:39473)
Incoming α-D-GalpA-(1→4)-α-D-GalpA(2−) (CHEBI:39473) is conjugate base of α-D-GalpA-(1→4)-α-D-GalpA (CHEBI:40583)
IUPAC Names
(α-D-galactopyranosyluronic acid)-(1→4)-α-D-galactopyranuronic acid
4-O-(α-D-galactopyranosyluronic acid)-α-D-galactopyranuronic acid
α-D-galactopyranuronosyl-(1→4)-α-D-galactopyranuronic acid
Synonyms Sources
4-O-alpha-D-Galactopyranuronosyl-alpha-D-galactopyranuronic acid ChemIDplus
4-O-α-D-galactopyranuronosyl-α-D-galactopyranuronic acid ChEBI
α-D,α-D-digalacturonic acid ChEBI
α-D-GalA-(1→4)-α-D-GalA ChEBI
α-D-galacturonosyl-(1→4)-α-D-galacturonic acid ChEBI
Digalacturonic acid ChemIDplus
DIGALACTURONIC ACID PDBeChem
O-(alpha-D-Galactopyranosyluronic acid)-(1-4)-alpha-D-galactopyranuronic acid ChemIDplus
pectin disaccharide ChEBI
Manual Xref Database
AD0 PDBeChem
View more database links
Registry Numbers Types Sources
1442091 Reaxys Registry Number Reaxys
28144-27-6 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
7954511 PubMed citation Europe PMC
Last Modified
13 June 2018