Summary
SMILES: CCCCCCCCCCCCC/C=C/[C@H](C(NC(=O)CCCCCCCCCCCCCCCCCCCCCCCC)CO[C@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O[C@@H]1O[C@H](CO)[C@@H]([C@@H]([C@H]1O)O)O[C@H]1O[C@H](CO)[C@@H]([C@@H]([C@H]1O)O[C@@H]1O[C@H](CO)[C@@H]([C@@H]([C@H]1NC(=O)C)O)O)O)OInChI: InChI=1S/C69H128N2O23/c1-4-6-8-10-12-14-16-18-19-20-21-22-23-24-25-26-28-30-32-34-36-38-40-53(78)71-47(48(77)39-37-35-33-31-29-27-17-15-13-11-9-7-5-2)45-87-67-60(84)58(82)63(51(43-74)90-67)92-68-61(85)59(83)64(52(44-75)91-68)93-69-62(86)65(56(80)50(42-73)89-69)94-66-54(70-46(3)76)57(81)55(79)49(41-72)88-66/h37,39,47-52,54-69,72-75,77,79-86H,4-36,38,40-45H2,1-3H3,(H,70,76)(H,71,78)/b39-37+/t47?,48-,49-,50-,51-,52-,54-,55+,56+,57-,58-,59-,60-,61-,62-,63-,64+,65+,66+,67+,68+,69-/m1/s1InChIKey: BIDGDAHARPMCIU-CEBHBINMSA-N
DeepSMILES: CCCCCCCCCCCCC/C=C/[C@H]CNC=O)CCCCCCCCCCCCCCCCCCCCCCCC))))))))))))))))))))))))))CO[C@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O[C@@H]O[C@H]CO))[C@@H][C@@H][C@H]6O))O))O[C@H]O[C@H]CO))[C@@H][C@@H][C@H]6O))O[C@@H]O[C@H]CO))[C@@H][C@@H][C@H]6NC=O)C))))O))O)))))))O))))))))))))))))))O
Scaffold Graph/Node/Bond level: C1CCC(OC2CCOC(OC3CCC(OC4CCCOC4)OC3)C2)OC1
Scaffold Graph/Node level: C1CCC(OC2CCOC(OC3CCC(OC4CCCOC4)OC3)C2)OC1
Scaffold Graph level: C1CCC(CC2CCC(CC3CCCC(CC4CCCCC4)C3)CC2)CC1
Functional groups: C/C=C/C; CC(=O)NC; CNC(C)=O; CO; CO[C@@H](C)OC; CO[C@H](C)OC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Sphingolipids
ClassyFire Subclass: Glycosphingolipids
NP Classifier Biosynthetic pathway: Fatty acids
NP Classifier Superclass: Sphingolipids
NP Classifier Class: Neutral glycosphingolipids
Synonymous chemical names:globoside
External chemical identifiers:CID:102601546
Chemical structure download
