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CHEBI:27931 - α-maltotriose

ChEBI IDCHEBI:27931
ChEBI Nameα-maltotriose
Stars
ASCII Namealpha-maltotriose
DefinitionA maltotriose trisaccharide in which the glucose residue at the reducing end is in the pyranose ring form and has α configuration at the anomeric carbon atom..
Secondary ChEBI IDsCHEBI:6672, CHEBI:25146, CHEBI:43937
Last Modified17 April 2015
DownloadsMolfile

FormulaC18H32O16
Net Charge0
Average Mass504.438
Monoisotopic Mass504.16903
SMILESOC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@@H](O[C@H]3[C@H](O)[C@@H](O)[C@@H](O)O[C@@H]3CO)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O
WURCSWURCS=2.0/1,3,2/[a2122h-1a_1-5]/1-1-1/a4-b1_b4-c1
InChIInChI=1S/C18H32O16/c19-1-4-7(22)8(23)12(27)17(31-4)34-15-6(3-21)32-18(13(28)10(15)25)33-14-5(2-20)30-16(29)11(26)9(14)24/h4-29H,1-3H2/t4-,5-,6-,7-,8+,9-,10-,11-,12-,13-,14-,15-,16+,17-,18-/m1/s1
InChIKeyFYGDTMLNYKFZSV-PXXRMHSHSA-N

Species of MetaboliteComponentSourceComments
Homo sapiens (ncbitaxon:9606) - DOI (10.1038/nbt.2488)
Roles Classification

ChEBI Ontology
IUPAC Name 
α-D-glucopyranosyl-(1→4)-α-D-glucopyranosyl-(1→4)-α-D-glucopyranose
Synonyms  Source
MaltotrioseKEGG COMPOUND
AmylotrioseKEGG COMPOUND
MALTOTRIOSEPDBeChem
α-D-Glcp-(1→4)-α-D-Glcp-(1→4)-α-D-GlcpIUPAC
UniProt Name  Source
α-maltotrioseUniProt
Manual XrefsDatabases
C01835KEGG COMPOUND
MLRPDBeChem
DB03277DrugBank
G96370VAGlyTouCan
G96370VAGlyGen
Registry NumbersSources
Beilstein:1275025Beilstein