CHEBI:147829 - α-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc

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ChEBI Name α-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc
ChEBI ID CHEBI:147829
ChEBI ASCII Name alpha-D-Manp-(1->4)-beta-D-GlcpNAc-(1->4)-D-GlcpNAc
Definition An amino trisaccharide consisting of α-D-mannopyranose, 2-acetamido-2-deoxy-β-D-glucopyranose and 2-acetamido-2-deoxy-D-glucopyranose residues joined in sequence by (1→4) glycosidic bonds.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Gareth Owen
Supplier Information
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Formula C22H38N2O16
Net Charge 0
Average Mass 586.544
Monoisotopic Mass 586.22213
InChI InChI=1S/C22H38N2O16/c1-6(28)23-11-14(31)18(9(4-26)36-20(11)35)39-21-12(24-7(2)29)15(32)19(10(5-27)38-21)40-22-17(34)16(33)13(30)8(3-25)37-22/h8-22,25-27,30-35H,3-5H2,1-2H3,(H,23,28)(H,24,29)/t8-,9-,10-,11-,12-,13-,14-,15-,16+,17+,18-,19-,20?,21+,22-/m1/s1
InChIKey OCPQLCXSCTTXMX-WZABUGRGSA-N
SMILES O1[C@@H](O[C@H]2[C@H](O)[C@@H](NC(=O)C)C(O[C@@H]2CO)O)[C@H](NC(=O)C)[C@@H](O)[C@H](O[C@H]3O[C@@H]([C@@H](O)[C@H](O)[C@@H]3O)CO)[C@H]1CO
ChEBI Ontology
Outgoing α-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc (CHEBI:147829) is a acetamides (CHEBI:22160)
α-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc (CHEBI:147829) is a amino trisaccharide (CHEBI:59266)
α-D-Manp-(1→4)-β-D-GlcpNAc-(1→4)-D-GlcpNAc (CHEBI:147829) is a glucosamine oligosaccharide (CHEBI:22485)
IUPAC Names
α-D-mannopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→4)-2-acetamido-2-deoxy-D-glucopyranose
Man(a1-4)GlcNAc(b1-4)GlcNAc
Synonyms Sources
α-D-manno-hexopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-gluco-hexopyranosyl-(1→4)-2-acetamido-2-deoxy-D-gluco-hexopyranose IUPAC
N-[(3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3-acetamido-4-hydroxy-6-(hydroxymethyl)-5-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,4-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide IUPAC
WURCS=2.0/3,3,2/[a2122h-1x_1-5_2*NCC/3=O][a2122h-1b_1-5_2*NCC/3=O][a1122h-1a_1-5]/1-2-3/a4-b1_b4-c1 SUBMITTER
Manual Xrefs Databases
G09280 KEGG GLYCAN
G18081AA GlyTouCan
G18081AA GlyGen
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Last Modified
20 May 2020