In-Silico Structure Database (LMISSD)

Systematic Name
Galβ1-3GalNAcβ1-4Galα1-4Galβ1-4Glcβ-Cer(d18:1/22:0)
LM ID
LMSP0502BK04
Status
Active (generated by computational methods)
Exact Mass
Calculate m/z
1472.896668
Formula

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MDLMOL SDF CSV TSV PNG
MDLMOL files can be opened in various drawing programs. In ChemDraw, open as filetype "MDL Molfile".

Main

Classification

Category
Main Class
Sub Class
Sphingolipids [SP]
Neutral glycosphingolipids [SP05]
Galalpha1-4Galbeta1-4Glc- (Globo series) [SP0502]

String Representations

InChiKey (Click to copy)
VYYDVIYRFGZEDT-ISQRFBDLSA-N
InChi (Click to copy)
InChI=1S/C72H132N2O28/c1-4-6-8-10-12-14-16-18-19-20-21-22-23-25-27-29-31-33-35-37-52(82)74-45(46(81)36-34-32-30-28-26-24-17-15-13-11-9-7-5-2)43-93-69-61(90)57(86)65(49(40-77)96-69)100-72-63(92)59(88)66(51(42-79)98-72)101-71-62(91)58(87)64(50(41-78)97-71)99-68-53(73-44(3)80)67(55(84)48(39-76)94-68)102-70-60(89)56(85)54(83)47(38-75)95-70/h34,36,45-51,53-72,75-79,81,83-92H,4-33,35,37-43H2,1-3H3,(H,73,80)(H,74,82)/b36-34+/t45-,46+,47?,48?,49?,50?,51?,53?,54-,55-,56-,57+,58+,59+,60?,61?,62?,63?,64-,65+,66-,67+,68-,69+,70-,71?,72-/m0/s1
SMILES (Click to copy)
CC(=O)NC1[C@@H](O[C@@H]2OC(CO)[C@H](O)[C@H](O)C2O)[C@@H](O)C(CO)O[C@H]1O[C@@H]1[C@H](O)C(O)[C@H](O[C@@H]2[C@H](O)C(O)[C@H](O[C@H]3[C@H](O)C(O)[C@H](OC[C@H](NC(=O)CCCCCCCCCCCCCCCCCCCCC)[C@H](O)/C=C/CCCCCCCCCCCCC)OC3CO)OC2CO)OC1CO

References

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 102
Rings 5
Aromatic Rings 0
Rotatable Bonds 52
Van der Waals Molecular Volume 1452.56
Topological Polar Surface Area 484.53
Hydrogen Bond Donors 18
Hydrogen Bond Acceptors 28
logP 10.61
Molar Refractivity 384.78