Structure Database (LMSD)
Common Name
sialyl-Lea(d18:1/24:0)
Systematic Name
NeuAcα2-3Galβ1-3(Fucα1-4)GlcNAcβ1-3Galβ1-4Glcβ-Cer(d18:1/24:0)
Synonyms
LM ID
LMSP0601DL05
Formula
Exact Mass
Calculate m/z
1776.028472
Sum Composition
Status
Active (generated by computational methods)
No other lipid differing only in stereochemistry/bond geometry found
3D model of sialyl-Lea(d18:1/24:0)
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)
PFYDVMQVAHVITB-GQJBLTRDSA-N
InChi (Click to copy)
InChI=1S/C85H153N3O35/c1-6-8-10-12-14-16-18-20-21-22-23-24-25-26-27-29-31-33-35-37-39-41-60(99)88-52(53(96)40-38-36-34-32-30-28-19-17-15-13-11-9-7-2)48-112-80-70(107)68(105)73(58(46-92)117-80)118-82-71(108)77(65(102)56(44-90)114-82)121-79-62(87-51(5)95)76(74(59(47-93)116-79)119-81-69(106)67(104)63(100)49(3)113-81)120-83-72(109)78(66(103)57(45-91)115-83)123-85(84(110)111)42-54(97)61(86-50(4)94)75(122-85)64(101)55(98)43-89/h38,40,49,52-59,61-83,89-93,96-98,100-109H,6-37,39,41-48H2,1-5H3,(H,86,94)(H,87,95)(H,88,99)(H,110,111)/b40-38+/t49-,52+,53-,54+,55-,56-,57-,58-,59-,61-,62-,63-,64-,65+,66+,67-,68-,69+,70-,71-,72-,73-,74-,75-,76-,77+,78+,79+,80-,81-,82+,83+,85+/m1/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](C)[C@@H](O)[C@@H](O)[C@@H]4O)[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]3NC(=O)C)[C@H]2O)[C@H](O)[C@H]1O)([H])(NC(CCCCCCCCCCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCCCCCC
References
Calculated Physicochemical Properties
Heavy Atoms
123
Rings
6
Aromatic Rings
0
Rotatable Bonds
60
Van der Waals Molecular Volume
1732.35
Topological Polar Surface Area
611.92
Hydrogen Bond Donors
22
Hydrogen Bond Acceptors
35
logP
11.31
Molar Refractivity
457.11
Reactions
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Admin
Created at
-
Updated at
26th Jul 2021