Structure Database (LMSD)
Systematic Name
Galα1-3(NeuAcα2-3Galβ1-4GlcNAcβ1-6)Galβ1-4Glcβ-Cer(d18:1/22:0)
Synonyms
LM ID
LMSP0601GS04
Formula
Exact Mass
Calculate m/z
1763.992087
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)
SLIPLTNQOIQTQL-XHJIVBJZSA-N
InChi (Click to copy)
InChI=1S/C83H149N3O36/c1-5-7-9-11-13-15-17-19-20-21-22-23-24-26-28-30-32-34-36-38-58(97)86-49(50(94)37-35-33-31-29-27-25-18-16-14-12-10-8-6-2)45-111-78-69(106)67(104)73(56(44-91)116-78)119-80-70(107)75(120-79-68(105)66(103)62(99)53(41-88)113-79)64(101)57(117-80)46-112-77-60(85-48(4)93)65(102)72(55(43-90)115-77)118-81-71(108)76(63(100)54(42-89)114-81)122-83(82(109)110)39-51(95)59(84-47(3)92)74(121-83)61(98)52(96)40-87/h35,37,49-57,59-81,87-91,94-96,98-108H,5-34,36,38-46H2,1-4H3,(H,84,92)(H,85,93)(H,86,97)(H,109,110)/b37-35+/t49-,50+,51-,52+,53+,54+,55+,56+,57+,59+,60+,61+,62-,63-,64-,65+,66-,67+,68+,69+,70+,71+,72+,73+,74+,75-,76-,77+,78+,79+,80-,81-,83-/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]3O[C@H](CO)[C@@H](O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O[C@]5(O[C@@]([H])([C@H](O)[C@H](O)CO)[C@H](NC(=O)C)[C@@H](O)C5)C(O)=O)[C@H]4O)[C@H](O)[C@H]3NC(=O)C)[C@H](O)[C@H](O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)[C@H]2O)[C@H](O)[C@H]1O)([H])(NC(CCCCCCCCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCCCCCC
References
Calculated Physicochemical Properties
Heavy Atoms
122
Rings
6
Aromatic Rings
0
Rotatable Bonds
59
Van der Waals Molecular Volume
1706.54
Topological Polar Surface Area
632.15
Hydrogen Bond Donors
23
Hydrogen Bond Acceptors
36
logP
9.79
Molar Refractivity
449.78
Admin
Created at
-
Updated at
26th Jul 2021