Structure Database (LMSD)
Common Name
galgactosyl-paraglobside(d18:1/26:0)
Systematic Name
Galβ1-3Galβ1-4GlcNAcβ1-3Galβ1-4Glcβ-Cer(d18:1/26:0)
Synonyms
LM ID
LMSP0505BJ06
Formula
Exact Mass
Calculate m/z
1528.959268
Sum Composition
Status
Active (generated by computational methods)
3D model of galgactosyl-paraglobside(d18:1/26:0)
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)
CEUFYYMHFPJOQE-BUKWTRQRSA-N
InChi (Click to copy)
InChI=1S/C76H140N2O28/c1-4-6-8-10-12-14-16-18-19-20-21-22-23-24-25-26-27-29-31-33-35-37-39-41-56(86)78-49(50(85)40-38-36-34-32-30-28-17-15-13-11-9-7-5-2)47-97-73-65(94)63(92)69(55(46-83)102-73)104-76-66(95)70(59(88)52(43-80)100-76)105-72-57(77-48(3)84)61(90)68(54(45-82)101-72)103-75-67(96)71(60(89)53(44-81)99-75)106-74-64(93)62(91)58(87)51(42-79)98-74/h38,40,49-55,57-76,79-83,85,87-96H,4-37,39,41-47H2,1-3H3,(H,77,84)(H,78,86)/b40-38+/t49-,50+,51+,52+,53+,54+,55+,57+,58-,59-,60-,61+,62-,63+,64+,65+,66+,67+,68+,69+,70-,71-,72-,73+,74-,75-,76-/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](O[C@@H]3O[C@H](CO)[C@@H](O[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]3NC(=O)C)[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
106
Rings
5
Aromatic Rings
0
Rotatable Bonds
56
Van der Waals Molecular Volume
1521.76
Topological Polar Surface Area
484.53
Hydrogen Bond Donors
18
Hydrogen Bond Acceptors
28
logP
12.17
Molar Refractivity
403.25
Admin
Created at
-
Updated at
26th Jul 2021