CHEBI:136776 - β-D-Glcp-(1→4)-β-D-Glcp-(1→4)-α-D-Glcp-(1→4)-α-D-GalpOCH2CH2NH2

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name β-D-Glcp-(1→4)-β-D-Glcp-(1→4)-α-D-Glcp-(1→4)-α-D-GalpOCH2CH2NH2
ChEBI ID CHEBI:136776
ChEBI ASCII Name beta-D-Glcp-(1->4)-beta-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-GalpOCH2CH2NH2
Definition An α-D-glucoside that is the 2-aminoethyl glycoside of a tetrasaccharide consisting of two β-D-glucosyl residues, an α-D-glucosyl residue and (at the reducing end) an α-D-galactosyl residue, all linked sequentially (1→4).
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C26H47NO21
Net Charge 0
Average Mass 709.647
Monoisotopic Mass 709.26406
InChI InChI=1S/C26H47NO21/c27-1-2-41-23-17(38)13(34)20(8(4-29)43-23)47-25-19(40)15(36)22(10(6-31)45-25)48-26-18(39)14(35)21(9(5-30)44-26)46-24-16(37)12(33)11(32)7(3-28)42-24/h7-26,28-40H,1-6,27H2/t7-,8-,9-,10-,11-,12+,13-,14-,15-,16-,17-,18-,19-,20+,21-,22-,23+,24+,25-,26+/m1/s1
InChIKey VWWLVYYAONNRIC-OLYGLWNMSA-N
SMILES [C@@H]1([C@@H]([C@H]([C@@H]([C@H](O1)CO)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O)O)O[C@H]3[C@@H]([C@H]([C@H](O[C@@H]3CO)O[C@@H]4[C@@H]([C@H]([C@H](O[C@@H]4CO)OCCN)O)O)O)O
ChEBI Ontology
Outgoing β-D-Glcp-(1→4)-β-D-Glcp-(1→4)-α-D-Glcp-(1→4)-α-D-GalpOCH2CH2NH2 (CHEBI:136776) is a α-D-galactoside (CHEBI:46953)
β-D-Glcp-(1→4)-β-D-Glcp-(1→4)-α-D-Glcp-(1→4)-α-D-GalpOCH2CH2NH2 (CHEBI:136776) is a tetrasaccharide derivative (CHEBI:63567)
IUPAC Name
2-aminoethyl β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-α-D-glucopyranosyl-(1→4)-α-D-galactopyranoside
Synonyms Sources
2-aminoethyl β-D-glucosyl-(1→4)-β-D-glucosyl-(1→4)-α-D-glucosyl-(1→4)-α-D-galactoside ChEBI
β-D-Glc-(1→4)-β-D-Glc-(1→4)-α-D-Glc-(1→4)-α-D-GalO[CH2]2NH2 ChEBI
β-D-Glc-(1→4)-β-D-Glc-(1→4)-α-D-Glc-(1→4)-α-D-GalOCH2CH2NH2 ChEBI
β-D-Glcp-(1→4)-β-D-Glcp-(1→4)-α-D-Glcp-(1→4)-α-D-GalpO[CH2]2NH2 IUPAC
Glcβ1-4Glcβ1-4Glcα1-4GalαOCH2CH2NH2 ChEBI
Manual Xref Database
AU2015323651 Patent
View more database links
Registry Number Type Source
29433968 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
28275152 PubMed citation Europe PMC
Last Modified
10 April 2017