CHEBI:144028 - α-D-Man-(1→6)-α-D-Man-(1→4)-α-D-glucosaminyl-(1→6)-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-2-acyl-inositol zwitterion

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
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ChEBI Name α-D-Man-(1→6)-α-D-Man-(1→4)-α-D-glucosaminyl-(1→6)-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-2-acyl-inositol zwitterion
ChEBI ID CHEBI:144028
ChEBI ASCII Name alpha-D-Man-(1->6)-alpha-D-Man-(1->4)-alpha-D-glucosaminyl-(1->6)-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-2-acyl-inositol zwitterion
Definition A glycosyl-phosphatidylinositol derivative where R1 can be an alkyl or an acyl group, R2 and R3 are both acyl groups of undefined composition.
Stars This entity has been manually annotated by a third party.
Submitter Lucila Aimo
Download Molfile XML SDF
Formula C29H47NO27PR3
Net Charge 0
Average Mass (excl. R groups) 872.649
Monoisotopic Mass (excl. R groups) 872.20731
SMILES [C@@H]1([C@@H]([C@@H]([C@@H]([C@H]([C@@H]1O)O)O)OC(=O)*)OP(OC[C@H](CO*)OC(=O)*)(=O)[O-])O[C@@H]2[C@H]([NH3+])[C@@H](O)[C@@H]([C@H](O2)CO)O[C@@H]3[C@H]([C@H]([C@@H]([C@H](O3)CO[C@@H]4[C@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O)O
ChEBI Ontology
Outgoing α-D-Man-(1→6)-α-D-Man-(1→4)-α-D-glucosaminyl-(1→6)-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-2-acyl-inositol zwitterion (CHEBI:144028) is a organic molecular entity (CHEBI:50860)
Incoming D-mannose-(α1→2)-D-mannose-(α1→6)-D-mannose-(α1→4)-D-glucosaminyl-(α1→6)-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-2-acyl-inositol zwitterion (CHEBI:144074) has functional parent α-D-Man-(1→6)-α-D-Man-(1→4)-α-D-glucosaminyl-(1→6)-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-2-acyl-inositol zwitterion (CHEBI:144028)
Synonyms Sources
α-D-mannosyl-(1→6)-α-D-mannosyl-(1→4)-α-D-glucosaminyl-(1→6)-1-phosphatidyl-2-acyl-D-myo-inositol SUBMITTER
an α-D-Man-(1→6)-α-D-Man-(1→4)-α-D-GlcN-(1→6)-(1-radyl,2-acyl-sn-glycero-3-phospho)-1D-myo-2-acyl-inositol UniProt
H3 glycosylphosphatidyl(acyl)inositol SUBMITTER
Man-Man-GlcN-(acyl)PI SUBMITTER
Man-Man-GP(acyl)I SUBMITTER
Citation Waiting for Citations Type Source
15623507 PubMed citation SUBMITTER