CHEBI:137174 - α-D-Rhap4NFo-(1→3)-α-D-Rhap4NFo-(1→2)-α-D-Rhap4NFoO[CH2]5CO2Me

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name α-D-Rhap4NFo-(1→3)-α-D-Rhap4NFo-(1→2)-α-D-Rhap4NFoO[CH2]5CO2Me
ChEBI ID CHEBI:137174
ChEBI ASCII Name alpha-D-Rhap4NFo-(1->3)-alpha-D-Rhap4NFo-(1->2)-alpha-D-Rhap4NFoO[CH2]5CO2Me
Definition A glycoside that consists of three N-formyl-α-D-perosamine residues linked sequentially (1→3) and (1→2) and linked at the reducing end glycosidically to a 5-(methoxycarbonyl)pentyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C28H47N3O15
Net Charge 0
Average Mass 665.685
Monoisotopic Mass 665.30072
InChI InChI=1S/C28H47N3O15/c1-13-17(29-10-32)20(36)22(38)26(42-13)45-24-19(31-12-34)15(3)43-27(23(24)39)46-25-21(37)18(30-11-33)14(2)44-28(25)41-9-7-5-6-8-16(35)40-4/h10-15,17-28,36-39H,5-9H2,1-4H3,(H,29,32)(H,30,33)(H,31,34)/t13-,14-,15-,17-,18-,19-,20+,21+,22+,23+,24+,25+,26-,27-,28+/m1/s1
InChIKey VQLAQYQYICCAHP-UAZIWKOSSA-N
SMILES [C@H]1([C@H]([C@H]([C@@H]([C@H](O1)C)NC([H])=O)O)O)O[C@@H]2[C@@H]([C@H](O[C@@H]([C@H]2NC([H])=O)C)O[C@@H]3[C@H](O[C@@H]([C@H]([C@@H]3O)NC([H])=O)C)OCCCCCC(OC)=O)O
ChEBI Ontology
Outgoing α-D-Rhap4NFo-(1→3)-α-D-Rhap4NFo-(1→2)-α-D-Rhap4NFoO[CH2]5CO2Me (CHEBI:137174) has functional parent α-D-Rhap4NFo-(1→3)-α-D-Rhap4NFo-(1→2)-α-D-Rhap4NFo (CHEBI:85396)
α-D-Rhap4NFo-(1→3)-α-D-Rhap4NFo-(1→2)-α-D-Rhap4NFoO[CH2]5CO2Me (CHEBI:137174) is a glycoside (CHEBI:24400)
α-D-Rhap4NFo-(1→3)-α-D-Rhap4NFo-(1→2)-α-D-Rhap4NFoO[CH2]5CO2Me (CHEBI:137174) is a methyl ester (CHEBI:25248)
α-D-Rhap4NFo-(1→3)-α-D-Rhap4NFo-(1→2)-α-D-Rhap4NFoO[CH2]5CO2Me (CHEBI:137174) is a trisaccharide derivative (CHEBI:63571)
IUPAC Names
methyl 6-{[4,6-dideoxy-4-formamido-α-D-mannopyranosyl-(1→3)-4,6-dideoxy-4-formamido-α-D-mannopyranosyl-(1→2)-4,6-dideoxy-4-formamido-α-D-mannopyranosyl]oxy}hexanoate
methyl 6-{[4-deoxy-4-formamido-α-D-rhamnopyranosyl-(1→3)-4-deoxy-4-formamido-α-D-rhamnopyranosyl-(1→2)-4-deoxy-4-formamido-α-D-rhamnopyranosyl]oxy}hexanoate
Synonyms Sources
5-methoxycarbonylpentyl 4,6-dideoxy-4-formamido-α-D-mannopyranosyl-(1→3)-4,6-dideoxy-4-formamido-α-D-mannopyranosyl-(1→2)-4,6-dideoxy-4-formamido-α-D-mannopyranoside ChEBI
5-methoxycarbonylpentyl N-formyl-α-D-perosaminyl-(1→3)-N-formyl-α-D-perosaminyl-(1→2)-N-formyl-α-D-perosaminide ChEBI
α-D-Rha4NFo-(1→3)-α-D-Rha4NFo-(1→2)-α-D-Rha4NFoO[CH2]5CO2Me ChEBI
α-D-Rha4NFo-(1→3)-α-D-Rha4NFo-(1→2)-α-D-Rha4NFoOCH2CH2CH2CH2CH2CO2Me ChEBI
α-D-Rhap4NFo-(1→3)-α-D-Rhap4NFo-(1→2)-α-D-Rhap4NFoOCH2CH2CH2CH2CH2CO2Me IUPAC
methyl 6-{[N-formyl-α-D-perosaminyl-(1→3)-N-formyl-α-D-perosaminyl-(1→2)-N-formyl-α-D-perosaminyl]oxy}hexanoate ChEBI
Registry Number Type Source
27628877 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
25263136 PubMed citation Europe PMC
28338626 PubMed citation Europe PMC
Last Modified
30 May 2017