Structure Database (LMSD)
Systematic Name
GalNAcβ1-4(NeuGcα2-3)Galβ1-4Glcβ-Cer(d18:1/26:0)
Synonyms
LM ID
LMSP0601CI06
Formula
Exact Mass
Calculate m/z
1511.943952
Sum Composition
Status
Active (generated by computational methods)
No other lipid differing only in stereochemistry/bond geometry found
3D model of
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Main
Classification
Category
Main Class
Sub Class
String Representations
InChiKey (Click to copy)
QUHZMDMFYCGHAZ-VJMRSZEASA-N
InChi (Click to copy)
InChI=1S/C75H137N3O27/c1-4-6-8-10-12-14-16-18-19-20-21-22-23-24-25-26-27-29-31-33-35-37-39-41-57(88)77-50(51(85)40-38-36-34-32-30-28-17-15-13-11-9-7-5-2)48-98-72-65(94)64(93)67(55(45-81)100-72)102-73-66(95)70(68(56(46-82)101-73)103-71-60(76-49(3)84)63(92)62(91)54(44-80)99-71)105-75(74(96)97)42-52(86)59(78-58(89)47-83)69(104-75)61(90)53(87)43-79/h38,40,50-56,59-73,79-83,85-87,90-95H,4-37,39,41-48H2,1-3H3,(H,76,84)(H,77,88)(H,78,89)(H,96,97)/b40-38+/t50-,51+,52-,53+,54+,55+,56+,59+,60+,61+,62-,63+,64+,65+,66+,67+,68-,69+,70+,71-,72+,73-,75-/m0/s1
SMILES (Click to copy)
[C@](CO[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O[C@@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3NC(=O)C)[C@H](O[C@]3(O[C@@]([H])([C@H](O)[C@H](O)CO)[C@H](NC(=O)CO)[C@@H](O)C3)C(O)=O)[C@H]2O)[C@H](O)[C@H]1O)([H])(NC(CCCCCCCCCCCCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCCCCCC
References
Calculated Physicochemical Properties
Heavy Atoms
105
Rings
4
Aromatic Rings
0
Rotatable Bonds
58
Van der Waals Molecular Volume
1513.75
Topological Polar Surface Area
489.94
Hydrogen Bond Donors
18
Hydrogen Bond Acceptors
27
logP
11.52
Molar Refractivity
398.78
Admin
Created at
-
Updated at
26th Jul 2021