CHEBI:136741 - β-D-GlcpA-(1→4)-β-D-Glcp-(1→4)-α-D-Glcp-(1→4)-α-D-GalpO[CH2]5NH2

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name β-D-GlcpA-(1→4)-β-D-Glcp-(1→4)-α-D-Glcp-(1→4)-α-D-GalpO[CH2]5NH2
ChEBI ID CHEBI:136741
ChEBI ASCII Name beta-D-GlcpA-(1->4)-beta-D-Glcp-(1->4)-alpha-D-Glcp-(1->4)-alpha-D-GalpO[CH2]5NH2
Definition An α-D-galactoside that is the 5-aminopentyl glycoside of a tetrasaccharide consisting of β-D-glucuronosyl, β-D-glucosyl, α-D-glucosyl and α-D-galactosyl residues linked sequentially (1→4).
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C29H51NO22
Net Charge 0
Average Mass 765.710
Monoisotopic Mass 765.29027
InChI InChI=1S/C29H51NO22/c30-4-2-1-3-5-45-26-18(40)14(36)21(9(6-31)46-26)49-27-19(41)15(37)22(10(7-32)47-27)50-28-20(42)16(38)23(11(8-33)48-28)51-29-17(39)12(34)13(35)24(52-29)25(43)44/h9-24,26-29,31-42H,1-8,30H2,(H,43,44)/t9-,10-,11-,12+,13+,14-,15-,16-,17-,18-,19-,20-,21+,22-,23-,24+,26+,27-,28+,29-/m1/s1
InChIKey PNXOBYQYNUFSII-KPEFKLFASA-N
SMILES O[C@H]1[C@@H]([C@H]([C@@H](O[C@@H]1C(O)=O)O[C@H]2[C@@H]([C@H]([C@@H](O[C@@H]2CO)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)OCCCCCN)O)O)O)O)O)O)O)O
ChEBI Ontology
Outgoing β-D-GlcpA-(1→4)-β-D-Glcp-(1→4)-α-D-Glcp-(1→4)-α-D-GalpO[CH2]5NH2 (CHEBI:136741) is a α-D-galactoside (CHEBI:46953)
β-D-GlcpA-(1→4)-β-D-Glcp-(1→4)-α-D-Glcp-(1→4)-α-D-GalpO[CH2]5NH2 (CHEBI:136741) is a tetrasaccharide derivative (CHEBI:63567)
IUPAC Name
5-aminopentyl β-D-glucopyranuronosyl-(1→4)-β-D-glucopyranosyl-(1→4)-α-D-glucopyranosyl-(1→4)-α-D-galactopyranoside
Synonyms Sources
5-aminopentyl (β-D-glucopyranosyluronic acid)-(1→4)-β-D-glucopyranosyl-(1→4)-α-D-glucopyranosyl-(1→4)-α-D-galactopyranoside IUPAC
5-aminopentyl β-D-glucuronosyl-(1→4)-β-D-glucosyl-(1→4)-α-D-glucosyl-(1→4)-α-D-galactoside ChEBI
β-D-GlcA-(1→4)-β-D-Glc-(1→4)-α-D-Glc-(1→4)-α-D-GalO[CH2]5NH2 ChEBI
GlcAβ1-4Glcβ1-4Glcα1-4GalαO[CH2]5NH2 ChEBI
Manual Xrefs Databases
AU2015323651 Patent
EP3000820 Patent
View more database links
Registry Number Type Source
29433906 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
28275152 PubMed citation Europe PMC
Last Modified
06 April 2017