EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C44H75NO36 |
| Net Charge | 0 |
| Average Mass | 1194.055 |
| Monoisotopic Mass | 1193.40688 |
| SMILES | CC(=O)N[C@H]1[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@@H](O)O[C@@H]2CO)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[C@H]3O[C@H](CO[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]4O[C@H]4O[C@H](CO)[C@@H](O)[C@H](O[C@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]5O)[C@@H]4O)[C@@H](O)[C@H](O)[C@@H]3O)[C@@H](O)[C@H](O)[C@@H]2O)[C@@H]1O |
| WURCS | WURCS=2.0/4,7,6/[a2122h-1a_1-5][a2122h-1b_1-5_2*NCC/3=O][a1122h-1b_1-5][a1122h-1a_1-5]/1-2-3-4-4-4-4/a4-b1_b4-c1_c6-d1_d6-e1_e2-f1_f3-g1 |
| InChI | InChI=1S/C44H75NO36/c1-9(51)45-17-23(57)34(14(6-50)75-39(17)78-35-13(5-49)71-38(68)29(63)28(35)62)79-42-32(66)26(60)21(55)16(77-42)7-69-40-30(64)25(59)20(54)15(76-40)8-70-44-37(27(61)19(53)11(3-47)74-44)81-43-33(67)36(22(56)12(4-48)73-43)80-41-31(65)24(58)18(52)10(2-46)72-41/h10-44,46-50,52-68H,2-8H2,1H3,(H,45,51)/t10-,11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24+,25+,26+,27+,28-,29-,30+,31+,32+,33+,34-,35-,36+,37+,38+,39+,40+,41-,42+,43-,44+/m1/s1 |
| InChIKey | PLUWHWOKRDDFIP-WWTVEKJASA-N |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| N-[(2S,3R,4R,5S,6R)-5-[(2S,3S,4S,5S,6R)-6-[[(2S,3S,4S,5S,6R)-6-[[(2S,3S,4S,5S,6R)-3-[(2R,3S,4S,5R,6R)-3,5-Dihydroxy-6-(hydroxymethyl)-4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]acetamide (CHEBI:152301) is a oligosaccharide (CHEBI:50699) |
| Synonyms | Source |
|---|---|
| alpha-D-manno-hexopyranosyl-(1->3)-alpha-D-manno-hexopyranosyl-(1->2)-alpha-D-manno-hexopyranosyl-(1->6)-alpha-D-manno-hexopyranosyl-(1->6)-beta-D-manno-hexopyranosyl-(1->4)-2-acetamido-2-deoxy-beta-D-gluco-hexopyranosyl-(1->4)-alpha-D-gluco-hexopyranose | SUBMITTER |
| Man(a1-3)Man(a1-2)Man(a1-6)Man(a1-6)Man(b1-4)GlcNAc(b1-4)a-Glc | SUBMITTER |